Mechanical stretch: physiological and pathological implications for human vascular endothelial cells
© Jufri et al. 2015
Received: 25 May 2015
Accepted: 25 August 2015
Published: 18 September 2015
Vascular endothelial cells are subjected to hemodynamic forces such as mechanical stretch due to the pulsatile nature of blood flow. Mechanical stretch of different intensities is detected by mechanoreceptors on the cell surface which enables the conversion of external mechanical stimuli to biochemical signals in the cell, activating downstream signaling pathways. This activation may vary depending on whether the cell is exposed to physiological or pathological stretch intensities. Substantial stretch associated with normal physiological functioning is important in maintaining vascular homeostasis as it is involved in the regulation of cell structure, vascular angiogenesis, proliferation and control of vascular tone. However, the elevated pressure that occurs with hypertension exposes cells to excessive mechanical load, and this may lead to pathological consequences through the formation of reactive oxygen species, inflammation and/or apoptosis. These processes are activated by downstream signaling through various pathways that determine the fate of cells. Identification of the proteins involved in these processes may help elucidate novel mechanisms involved in vascular disease associated with pathological mechanical stretch and could provide new insight into therapeutic strategies aimed at countering the mechanisms’ negative effects.
Blood vessels consist of three primary layers: the tunica intima, the tunica media and the tunica adventitia. The tunica intima is the innermost layer that contains the endothelium (endothelial cell (EC) layers) that provides a smooth surface for blood flow, whereas the tunica media contains thick layers of elastin, collagen and smooth muscle cells (SMCs) for vascular dilation or constriction. The outermost layer, the tunica adventitia, is composed of a mixture of connective tissue, collagen and elastic fibers and is used for arterial support. Hemodynamic forces, such as shear and tensile stress, continuously act upon blood vessels due to the pumping motion of the heart. Specifically, shear stress arises from the friction of the blood flow with the endothelial layer, whereas tensile stress primarily acts upon the medial layers and is due to the pulsatile nature of blood pumped from the heart.
Mechanical stretch enables vascular maintenance through proliferation, angiogenesis, the formation of reactive oxygen species, control of vascular tone and vascular remodeling [1–6]. However, the excessive mechanical stretch that occurs during hypertension has been shown to be detrimental as it perturbs these processes and causes inappropriate cellular responses that can lead to cardiovascular abnormalities . As such, mechanical stretch has been modeled in vitro by regulating stretch intensity to simulate physiological and pathological stretch magnitudes (the percentage of the cell elongation from the cell’s original dimensions). Low magnitude stretches of 5–10 % are categorized as physiological stretch, whereas high magnitude stretches of 20 % and above are considered pathological stretch and are thought to simulate what is proposed to occur during hypertension . The differences in stretch intensity may activate different downstream signaling pathways that determine the cells’ functional, biological and phenotypic features.
Mechanical stretch induces various biological processes in endothelial cells
Yoshigi et al. 2003 
Cells oriented 65 ° to stretch direction
Barron et al. 2007 
Cells oriented 47.8 ° at 100 %
Takemasa et al. 1998 
Cells oriented at 70/90 °
Wang et al. 2001 
Cells oriented at 60–70 ° at 10–15 % stretch
Haghighipour et al. 2010 
Perpendicular cell’s orientation
Moretti et al. 2004 
Paxillin needed for initial cell orientation
Huang et al. 2012 
Rho proteins for perpendicular alignment
Kaunas et al. 2005 
↑ JNK (2.6-fold) at 30 min
Kaunas et al. 2006 
↑ CAMP (3-fold)
Yamada et al. 2000 
Local stretch by microneedle
↑ Src homology 2-containing tyrosine phosphatase
Ueki et al. 2009 
↑ Hsp 25 (relative activity 40 %)
Luo et al. 2007 
↑ Hsp 70 (relative activity 60 %)
↑ JNK (5-fold)
Hsu et al. 2010 
↑ ERK (4-fold)
↑ p38 (4-fold)
Naruse et al. 1998 
↑ Ca2+ (2-fold) via transient receptor potential vanilloid 4
Thodeti et al. 2009 
↑ Ca2+ via transient receptor potential channels
Berrout et al. 2012 
↑ c-src (3.2-fold) at 15 min
Naruse et al. 1998 
Naruse et al. 1998 
↑ p21ras (24.7 % ratio) at 1 min
Ikeda et al. 1999 
↑ tyrosine phosphorylation (>2000 arbitrary unit)
Katanosaka et al. 2008 
↑ ERK at 15 mins
Shi et al. 2007 
↑ integrin beta-3 (171 %) at 4 h
Suzuki et al. 1997 
↑ Akt phosphorylation at 5 %, 10 min (6000 arbitrary unit)
Kou et al. 2009 
↑ Akt phosphorylation at 20 %, 30 min (1000 arbitrary unit)
↑ Akt phosphorylation and ↑ Bad phosphorylation in presence of TNFα at 6 %
Liu et al. 2003 
↑ Akt phosphorylation at Ser 473 at 30–60 mins
Nishimura et al. 2006 
↑ S6K phosphorylation (1.5-fold) at 30 mins
Li and Sumpio 2005 
↑ Rac1 (5-fold)
Liu et al. 2007 
↑ c-Myc (2–3-fold) at 1–2 h
Hurley et al. 2010 
↑ Egr-1 (5.5-fold) at 90 mins
Zhang et al. 2013 
↑ MMP-2 (3.7-fold) at 18 h
Wang et al. 2003 
↑ MMP-14 (3-fold) at 18 h
↑ MMP-2 (8-fold) at 8 h
von Offenberg Sweeney et al. 2004 
↑ pro MMP-2
Shukla et al. 2004 
↑ MCP-1 (200 %) at 6 h
Demicheva et al. 2008 
↑ IL-6 (3-fold) at 90 min
Kobayashi et al. 2003 
↑ COX-2 (2.5-fold) at 3 h
Zhao et al. 2009 
↑ thromboxane A2 synthase (150 %)
↑ von Willebrand factor to 5 mU/L at 60 min
Xiong et al. 2013 
↑ IL-8 (2.6-fold)
Okada et al. 1998 
↑ MCP-1 (2.8-fold)
↓ MCP-1 by exposure of nitric oxide donor
Wung et al. 2001 
MMP-9 silencing block migration and tube formation
von Offenberg Sweeney et al. 2005 
Endothelial cord aligning to 67.5–90°
Joung et al. 2006 
↑ Ang-2 (4.8-fold)
Yung et al. 2009 
PDGF-ββ (↑ 5.0-fold)
↑ VEGF (1.4-fold)
Zheng et al. 2001 
↑ VEGF-R2 (3.2-fold)
Zheng et al. 2008 
↑ Tie-2 (1.8-fold)
Wilkins et al. 2014 
↑ Flk-1 (1.7-fold)
Zheng et al. 2004 
↑ Tie-1 (2-fold)
↑ Tie-2 (1.9-fold)
↑ Alpha smooth muscle actin (1.6-fold)
Shoajei et al. 2014 
↑ Smooth muscle myosin heavy chain (1.3-fold)
↑ Alpha smooth muscle actin (165 %)
Cevallos et al. 2006 
↑ Caldesmon-1 (443 %)
↑ Smooth muscle myosin heavy chain (205 %)
↑ Calponin-1 (174 %)
↑ Young’s modulus of elasticity
Hatami et al. 2013 
↑ eNOS phosphorylation (1.8 arbitrary unit)
Takeda et al. 2006 
↑ NO (1.4-fold)
↑ eNOS (7-fold) at 50 %
Hu et al. 2013 
↑ Et-1 (2.3-fold)
Cheng et al. 2001 
↑ Et-1 (1.6-fold)
Toda et al. 2008 
↑ 8,9-epoxyeicosatrienoic acid (EET) (4–8-fold)
Fisslthaler et al. 2001 
↑ glutathione peroxidase to 200 %
Wagner et al. 2009 
↑ p66Shc (150–200-fold)
Spescha et al. 2014 
↓ Nox4 (40 %) 12 %, 24 h
Goettsch et al. 2009 
↑ eNOS (3-fold) at 12 %, 24 h
↑ NO (2 uM) at 5 %, 24 h
↑ ROS (221 %), 6 h
Ali et al. 2004 
↑ FAK phosphorylation
Ali et al. 2006 
Mechanical stretch receptors induce signal transduction
Mechanical stretch generates a cascade of biochemical signaling processes in ECs. The fundamental paradigm is that mechanoreceptors on the plasma membrane of ECs, through a series of signaling pathways, induce gene expression and protein synthesis to promote or ablate processes such as angiogenesis, proliferation, inflammation, apoptosis, vascular tone and cell survival.
Biochemically, mechanotransduction of stretch is detected by three known mechanoreceptor proteins that are distributed throughout the cell: stretch activated (SA) channel, integrin proteins and the platelet endothelial cell adhesion molecule-1 (PECAM). The SA channel is located on the plasma membrane and has been shown to participate in calcium (Ca2+) influx in response to stretch that later initiates PI3K activation mediated by Rho and Rho-associated kinase (ROCK) for cellular orientation [13, 14]. Studies on the SA channel have determined that the specific ion channel known as the transient receptor potential (TRP) is responsible for the Ca2+ influx . The transient receptor potential vanilloid channel 4 (TRPV4) is found to be highly expressed in ECs. Meanwhile, brain ECs specifically exhibit transient receptor potential classical 1 (TRPC1) and transient receptor potential polycystin 2 (TRPP2) . Knockdown of TRPP2 has been found to inhibit the Ca2+ influx, and this leads to disruption of blood–brain barrier integrity and to edema .
Integrins are the second known type of mechanoreceptors that act by transmitting stretch signals from the ECM into the cell. Integrins are transmembrane heterodimeric glycoproteins consisting of one of 8 different α and one of 18 different β subunits. They attach the cell to the ECM and to proteins located within the matrix (e.g., latent TGFβ1 for ITGB6). Stretch-exposed HUVECs express higher levels of the endothelial cell integrin αVβ3 through P13K activation, suggesting enhanced adhesiveness of the cells to RGD (tripeptide of L-arginine, glycine, and L-aspartic acid)-containing ECM substrates such as fibronectin [17, 18]. As integrin-ECM binding is increased, it stimulates an increased level of Ca2+ influx that is associated with promoting phosphorylation of focal adhesion kinase (FAK) and Src family kinases proximal to the inner surfaces of the integrin. FAK is one of the components of the focal adhesion complex which is composed of a group of proteins (i.e., zyxin, vinculin, talin, paxillin and actinin) that function together to connect the ECM and integrins to the cytoskeleton at the plasma membrane . In addition, mechanical stretch induces Src tyrosine kinase activation of molecules localized to the focal adhesion (FA), and this appears to be central to signal transduction pathways and changes actin organization in HUVECs .
The third class of proteins that act as a mechanoreceptors is the platelet endothelial cell adhesion molecule-1 (PECAM-1), also known as CD31. It is a cell adhesion molecule that is abundantly expressed in ECs, especially in regions of cell-to-cell contact . It is suggested that the application of a specific force generates EC deformation, and PECAM-1 is able to sense this change from the neighboring cells through PECAM-1 tyrosine phosphorylation. This is then followed by activation of the extracellular signal-related kinase 1/2 (ERK1/2) signaling cascade via P21ras and Raf-1 [21–23]. In addition, PECAM-1 phosphorylation initiates SHP-2 binding to activate MAPK and ERK1/2 pathways that promote cellular reorientation [24, 25]. Expression of these mechanoreceptor proteins across the EC indicates that sensing the force is a crucial initial step to activate mechanotransduction.
Morphology and structural changes induced by mechanical stretch
The perpendicular orientation of early phase ECs is mediated by paxillin, one of the signaling structural scaffold proteins found in the FA complex . Knockdown of paxillin abolishes the perpendicular orientation of stretched HUVECs, suggesting it plays a pivotal role in aligning stress fibers during stretch . Equally, stretching increases JNK and ERK phosphorylation during the early stages of stress fiber orientation, and these levels subside after the stress fiber is oriented perpendicular to the stretch direction [36, 37]. In addition, heat shock protein 70 (HSP70) expression has also been shown to be increased by stretch and its inhibition shown to inhibit EC stress fiber formation . Thus, these intracellular signals are suggestive of complex processes involved in the regulation of stress fibers in determining EC morphology when they are subjected to mechanical stretch.
Extracellular matrix remodeling by mechanical stretch
The ECM comprises a mixture of molecules, such as collagen, elastin, proteoglycans, laminin and fibronectin that provide structural support, adhesion sites and transmission of biochemical signals to surrounding cells . Synthesis and degradation of ECM is an essential part of the vascular remodeling process for homeostasis and during physiological and pathological responses. Zinc-dependent endopeptidases from the matrix metalloproteinase (MMP) protease family can induce the breakdown of ECM if the zymogen MMPs are activated physiologically [40–42]. MMPs contribute to vascular remodeling through vascular adaptation, angiogenesis and repair during physiological stretch. Physiological stretch increases MMP-2 expression in bovine arterial endothelial cells (BAEC), and this is thought to be mediated by the Gβγ/p38 and PTK/Shc/ERK pathways . By contrast, pathological stretch increases both MMP-2 and MMP-14 in HUVECs, and this was shown to be mediated through the TNF-α and JNK pathways [44, 45]. MMP activity during pathological stretch is thought to contribute to atherosclerosis as it facilitates the migration of vascular smooth muscle cells into the intima layer where further proliferation contributes to plaque formation .
Physiological stretch induces angiogenesis
Vascular ECs are known to play a major role in angiogenesis as they are involved in vessel cord formation, sprouting, migration and tube formation, and this appears to be facilitated by a series of chemical stimuli (Table 1). Several processes involved in angiogenesis have been associated with physiological stretch. For example, physiological stretch has been found to upregulate key tyrosine kinase receptors such as Flk-1, Tie-2 and Tie-1 in both HUVECs and RCMECs [47, 48]. These receptors are sensitive to growth factors and act to induce the formation of new blood vessel.
In addition, stretch stimulates the secretion of angiogenic factors that circulate in a paracrine or autocrine manner in the vascular system [49, 47]. Physiological stretch has been reported to increase the secretion of vascular endothelial growth factor (VEGF) and the expression of its receptor, VEGF-R2 (Flk-1) . Both of these are key proteins needed for cell proliferation and tube formation during HUVEC angiogenesis [50, 51]. In addition, basic fibroblast growth factor (bFGF) was also increased and found to promote sprouting during angiogenesis when ECs were subjected to stretch . bFGF may be released at the initial state of angiogenesis before being replaced by VEGF to complete the angiogenesis process . Furthermore, physiological stretch was found to activate endogenous biochemical molecules such as angiopoietin-2 and platelet derived growth factor ββ (PDGF-ββ) that may be involved in endothelial cell migration and sprout formation . EC migration and tube formation were also increased during stretch due to the activation of Gi protein subunits and increased GTPase activity which facilitates angiogenesis . Taken together, these results show that physiological stretch is intimately involved in evoking vasculature angiogenic processes across the vascular system.
Mechanical stretch stimulates EC proliferation
Cell proliferation is a fundamental process for replacing old and damaged cells and represents an important part of tissue homeostasis and stretch is thought to influence this biological function (Table 1). Exposure to physiological stretch in BAECs was found to induce cell proliferation, mediated by the P13K-dependent S6K mTOR-4E-BP1 pathway . The mammalian target of rapamycin (mTOR) is an important key translational pathway that regulates cell cycle, proliferation and growth. In addition, cell-to-cell adhesion is required for ECs to proliferate during stretch. This cell-to-cell adhesion is principally mediated by cadherins that transduce mechanical forces through Rac1 activation . This may limit stretch-mediated EC proliferation as it occurs only in the presence of adjacent cells and serves as a mechanism to prevent ECs from displaying elements of invasive behavior and/or excessive proliferation . However, uncontrolled proliferation of ECs has been observed in pathological stretch as the expression of the oncogene c-Myc was upregulated in HUVEC . This could be a major contributor to vascular disease as it could lead to the intimal thickening that increases vascular resistance and blood pressure. In addition, the observation that early growth response protein-1 (Egr-1) promotes proliferation during stretch in vein graft models supports the suggestion that pathological stretch plays a role in restenosis . Thus, future strategies aimed at targeting these proteins may be of therapeutic value for controlling cell proliferation that originates from hypertension.
Expression of vasoconstrictors and vasodilators during stretch
Blood vessels depend on numerous vasodilating and vasoconstricting protein factors to regulate vascular tone through the homeostatic balancing of blood pressure (Table 1). Endothelin 1 (ET-1) is a potent vasoconstrictor produced by vascular ECs. The endothelium-derived hyperpolarizing factor (EDHF) induced by epoxyeicosatrienoic acid (EET) generated by the cytochrome P450 (CYP) epoxygenase enzyme subfamily is another vasoconstrictor that functions to increase blood pressure [59, 60]. On the other hand nitric oxide (NO) plays an important role in vasodilation and is generated from the conversion of L-arginine to L-citrulline by phosphorylated endothelial nitric oxide synthase (eNOS) . The synthesis of eNOS is controlled by stretch, and its production is dependent on Ca2+ influx. Specifically, a decrease of Ca2+ elicited by an inhibitor of the SA channel was shown to inhibit eNOS phosphorylation . Physiological stretch was found to increase ET-1 mRNA levels in HUVECs, whereas EET and CYP 2C mRNA expression for the generation of EDHF was increased in the coronary artery of ECs . Pathological stretch was found to increase ET-1 in HUVECs [4, 64] whereas eNOS and NO were increased in BAECs and HUVECs [5, 62]. Several mechanisms have been proposed for the regulation of NO expression, such as an increase of Ca2+ concentration via the stretch-activated channel at the early phase of stretch followed by eNOS phosphorylation via the PKA pathway and activation of the P13K-Akt/PKB pathway in the late stage of stretch [5, 62, 65]. NO has anti-atherogenic properties, as it inhibits transcription factors that regulate expression of pro-atherogenic or pro-inflammatory genes. However, the balance of NO might be altered in pathological stretch as the ROS levels are often elevated significantly in this condition and results in reduced levels of NO. Thus, stretch intensity is an important factor in determining ROS balance to ensure healthy cellular function in the vascular system.
Increased production of reactive oxygen species by pathological stretch
Cells continuously produce ROS as a by-product of normal mitochondrial electron transfer. There are several forms of ROS, such as superoxide anions (O2 −), peroxynitrite anions (ONOO−) and hydroxyl radicals (−OH) with the most common being hydrogen peroxide (H2O2) a by-product of superoxide dismutation. At physiological concentrations, these short-lived reactive intermediates are involved in microbial defense, signal transduction and regulation of the cell cycle (Table 1). ROS act as second messengers in signal transduction cascades including those that mediate FAK phosphorylation and are necessary for cell motility and survival . Physiological stretch results in a decrease in superoxide anion production, as Nox4 expression is reduced in HUVECs. In ECs, Nox4-containing NAD(P)H oxidase complexes have been identified as a major source of superoxide anion formation. However, physiological stretch was found to suppress Nox4, increase NO release and reduce ROS formation, suggesting it performs a vasoprotective role . However, increased levels of ROS in pathological stretch can induce pro-atherogenic or pro-inflammatory conditions in HUVECs. Pathological stretch produces excessive O2 − that can react alone or through the enzyme superoxide dismutase to generate H2O2 . H2O2 later activates NFκB and the subsequent transcriptional activity of adhesion molecules such as VCAM-1. This promotes pro-inflammatory activity that leads to atherosclerosis formation over time . In addition, pathological stretch was found to phosphorylate p66Shc in HAEC, which leads to an increase of superoxide anions and a reduction of NO . p66Shc is an adaptor protein that mediates vascular dysfunction in hypertensive mice . Phosphorylation of p66Shc during pathological stretch disturbs the ROS balance as the superoxide anion reacts with NO to generate ONOO− . This results in reduced NO bioavailability and contributes to endothelial dysfunction as ECs lose NO-dependent anti-atherogenic properties . The findings indicate that pathological stretch is associated with excessive ROS production in ECs that can induce oxidative stress and eventually advance cardiovascular disease.
Interestingly, ECs have developed an adaptive mechanism of producing antioxidant enzymes during pathological stretch in HUVECs . For example, the glutathione peroxidase enzyme can degrade accumulating H2O2 resulting from the reaction of superoxide anion and NO that is involved in pro-inflammatory gene activation, thereby serving as an adaptive mechanism to protect cells from stress conditions. Furthermore, heat shock proteins (such as HSP10) may be upregulated in stretch-induced cells to ensure proper protein folding in response to stress that is thought to cause protein aggregation and misfolding . Thus, the expression of these proteins may serve as the cell’s protection against cellular injury although we suggest that their effect eventually wanes in response to the sustained production of ROS.
Mechanical stretch promotes inflammation in ECs
In pathological stretch, IL-8 can be secreted from the Weibel–Palade body’s storage granule that was highly exocytosed in HUVECs . In addition, IL-6 secretion has been shown to be mediated by the inflammatory transcription factor NFκB . The activation of NFκB results from the release of ROS to the cytoplasm that then reacts with Cu/Zn superoxide dismutase to form H2O2 that can subsequently activate NFκβ . Activation of NFκβ also activates adhesion molecules such as the vascular cell adhesion molecule 1 (VCAM-1) and intercellular adhesion molecule 1 (ICAM-1) that are pro-inflammatory. Additionally, application of mechanical stretch on the co-culture system of ECs and SMC showed that CD40 was also highly expressed in HUVECs . These surface molecules exert pro-inflammatory responses by recruiting monocytes or leukocytes, and their high expression predisposes patients to atherosclerotic plaque development. Taken together, evidence of expression of VCAM-1, ICAM-1 and IL-6/8 supports the proposition that mechanical stretch, especially at pathological intensity, stimulates protein expression associated with monocyte, leukocyte and T-cell recruitment and can lead to atherosclerosis as it stimulates the invasion and accumulation of white blood cells in the blood vessels (Table 1).
Apoptosis and survival of ECs during mechanical stretch
Cyclic stretch affects apoptosis and survival of ECs, and this appears to be based on the magnitude and duration of stretch applied to the cell (Table 1). Apoptosis of ECs is involved in plaque development by inducing inflammatory cell infiltration into the sub-endothelial layer of the vessel wall. In addition, luminal ECs in atherosclerotic plaques that undergo apoptosis are more likely to cause plaque erosion and rupture . Application of physiological stretch on BAEC was found to reduce apoptosis via P13K and Akt activation . This can be explained further by noting that Akt was phosphorylated in 5 % stretch, whereas when 20 % stretch was applied to HAEC, Akt was dephosphorylated . Akt promotes cell survival as it enables the phosphorylation of the pro-apoptotic protein BAD from inducing cell death in BAEC . In addition, expression of NADPH oxidase subunit p22phox in stretched ECs is found to increase ECs survival as p22phox gene knockdown induces pro-apoptotic caspase-3. The discrepancies between physiological and pathological stretch in the promotion of apoptosis indicate that physiological stretch plays a vasculoprotective role whereas pathological stretch plays a role in the promotion of EC apoptosis .
Pathological implications of mechanical stretch
As high-intensity stretch introduces a stressful environment to the blood vessels, they are modified to accommodate this by a collective process that has been termed ‘vascular remodeling’. This process involves vascular alteration in the form of migration, proliferation, apoptosis and ECM reorganization involving ECM synthesis and degradation . However, degradation of ECM in blood vessels is related to the development of atherosclerosis as a result of smooth muscle cells migrating into the intima layer due to degradation of the internal elastic lamina in the tunica intima and the subsequent initiation of plaque formation . Chronic hypertension, a state associated with prolonged pathological stretch, promotes pro-inflammatory responses by cytokines (IL-8, IL-6) and MCP-1 and results in recruitment of neutrophils and monocytes to the vessel, leading to the development of atherosclerotic plaques . The accumulation of inflammatory cells at the site of inflammation acts as an initial event for fatty streak or atherosclerotic lesion formation and later induces SMC proliferation and migration into the intima layer leading to intimal thickening . Furthermore, mechanical stretch is found to increase EC stiffening which may exacerbate atherosclerosis . Interestingly, trans-differentiation of ECs to SMCs has been observed when stretch is applied to cells. Specifically, SMC marker genes (SM22-α, α-SMA, caldesmon-1, SM MHC and calponin) were increased by stretch, whereas a subsequent reduction in endothelial markers was observed [83, 84]. The presence of SMC markers on EC suggests EC plasticity towards SMC phenotype occurs during mechanical stretch, and this may contribute to the development of atherosclerosis.
As has been mentioned previously, pathological stretch could increase ROS production. This will in turn induce endothelial dysfunction and act as the initial step of atherogenesis. Endothelial dysfunction is an early indicator of atherogenesis that is characterized by reduced NO production that promotes platelet aggregation, thrombus formation and alterations in vasodilation . Excessive ROS production leads to oxidative stress, which in turn leads to oxidation of low-density lipoproteins, the uptake of which by macrophages is easily compared with non-oxidized lipoproteins in the formation of atheroma. Furthermore, ROS can also alter ECs such that they exhibit a pro-inflammatory phenotype characterized by the overexpression of MCP-1 and VCAM-1 . This attracts inflammatory cells, such as white blood cells, and results in the formation of fatty streaks on the tunica intima during atherosclerosis development.
Stenosis is a common vascular pathology characterized by the narrowing of a blood vessel due to atherosclerosis. Stenosis is treated by the use of balloon angioplasty or stents to widen the vessel. Balloon angioplasty reduces the recurrence of restenosis by 40 %, whereas treatment using stents reduces the recurrence of restenosis by 25 % . It is thought that stretching plays a role in this process by increasing cell proliferation and intimal thickening at the vascular graft area after the treatment, although this has yet to be conclusively proven [81, 87]. As previously mentioned, identification of the Egr-1 gene in stretched cells may hold future therapeutic potential as this gene is involved in cell proliferation and silencing it may prevent this process .
Another vascular pathology that may be associated with stretch is aneurysm formation. Aneurysms are formed due to the weakening of blood vessels, and their rupture in the brain is considered a cause of strokes. Approximately 2–3.2 % of the general population of the world develops intracranial aneurysms, and the rupture of aneurysms affects approximately 6 per 100,000 people per year [88–90]. Excessive stress could exacerbate the conditions leading to aneurysm rupture as there is a weakening of the vascular structure due to ECM degradation by MMP and cell apoptosis. The rupture of brain aneurysms has recently been reported to be caused by a mechanical force against the thin aneurysm wall . Thus, further study to elucidate mechanical stretch as the etiology for aneurysm development and rupture may assist in understanding aneurysm pathology.
The cells of the vascular system are exposed to complex environments and interact with various cell types, hormones, mechanical forces and other vasoactive substances. Due to the complexity of the cellular environment, it is particularly challenging to investigate specific outcomes from mechanical stretch of ECs. Thus, the application of stretch to ECs per se has unraveled protein signaling pathways and phenotypic changes as well as pathological consequences. It is therefore not surprising that designing experiments that simulate the conditions that exist in the vascular environment are near impossible. However, a reductionist approach has provided insight into some of mechanisms that can be pieced together to form a fragmented, although detailed, picture.
Shear stress and tensile stretch are two forces that are exerted on the vascular system, but these have contrasting effects on ECs, thus making it challenging to determine the precise mechanisms involved when both stimuli are applied . Therefore, a mechanical device capable of combining forces has been manufactured to explore its simultaneous effect on ECs [93, 92]. In addition, the application of co-culture systems can simulate more accurate complex vascular systems such as those in which ECs have close contact with SMCs. These approaches are still limited, but they may elucidate interactions between ECs and SMCs under conditions of mechanical stress. Outcomes may vary based on differences in stretch frequency, load cycle, amplitude, substrate rigidity and cell confluence [26, 34, 37, 94].
One recent addition to the “omics” suite dubbed “mechanomics” involves generating tools to map global molecular and cellular responses induced by mechanical forces . Application of these technologies could help elucidate comprehensive patterns of expression of genes (genomic), mRNA (transcriptomic), proteins (proteomic) and metabolites (metabolomics); however, the spatio-temporal nature of these technologies may be limiting. These technologies undoubtedly rely on a significant infrastructure and knowledge base, and, therefore, bioinformatics is an invaluable tool in teasing out the mechanistic implications of the protein and gene expression levels. As these fields continue to develop, combinations of gene expression, protein expression, metabolite data and transcriptomic data will provide a comprehensive understanding of stretch biology that will better illustrate the mechanotransduction processes .
Mechanical stretch involves various extracellular to intracellular changes in the coordination of ECs that leads to phenotypic changes in these cells. The response is dynamic such that aberrant changes lead to an imbalance in homeostasis and potentially lead to failure of function or undesired effects that can lead to hypertension and atherosclerosis, among other pathologies. ECs have complex adaptation mechanisms to counteract this stressful state, and a better understanding of these would be helpful in finding novel therapeutic approaches related to hypertension, atherosclerosis, restenosis and aneurysm formation.
This article was supported by Faculty of Medicine and Health Sciences, Macquarie University and a scholarship from the Malaysian Ministry of Education to Nurul F. Jufri.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Li W, Sumpio BE. Strain-induced vascular endothelial cell proliferation requires PI3K-dependent mTOR-4E-BP1 signal pathway. Am J Physiol Heart Circ Physiol. 2005;288(4):1591–7. doi:https://doi.org/10.1152/ajpheart.00382.2004.View ArticleGoogle Scholar
- Joung IS, Iwamoto MN, Shiu YT, Quam CT. Cyclic strain modulates tubulogenesis of endothelial cells in a 3D tissue culture model. Microvasc Res. 2006;71(1):1–11. doi:https://doi.org/10.1016/j.mvr.2005.10.005.View ArticlePubMedGoogle Scholar
- Birukov KG. Cyclic stretch, reactive oxygen species, and vascular remodeling. Antioxid Redox Signal. 2009;11(7):1651–67. doi:https://doi.org/10.1089/ars.2008.2390.PubMed CentralView ArticlePubMedGoogle Scholar
- Cheng TH, Shih NL, Chen SY, Loh SH, Cheng PY, Tsai CS, et al. Reactive oxygen species mediate cyclic strain-induced endothelin-1 gene expression via Ras/Raf/extracellular signal-regulated kinase pathway in endothelial cells. J Mol Cell Cardiol. 2001;33(10):1805–14. doi:https://doi.org/10.1006/jmcc.2001.1444.View ArticlePubMedGoogle Scholar
- Hu Z, Xiong Y, Han X, Geng C, Jiang B, Huo Y, et al. Acute mechanical stretch promotes eNOS activation in venous endothelial cells mainly via PKA and Akt pathways. PLoS One. 2013;8(8):e71359. doi:https://doi.org/10.1371/journal.pone.0071359.PubMed CentralView ArticlePubMedGoogle Scholar
- Lehoux S, Castier Y, Tedgui A. Molecular mechanisms of the vascular responses to haemodynamic forces. J Intern Med. 2006;259(4):381–92. doi:https://doi.org/10.1111/j.1365-2796.2006.01624.x.View ArticlePubMedGoogle Scholar
- Lal H, Verma S, Golden H, Foster D, Holt A, Dostal D. Molecular signaling mechanisms of myocardial stretch: implications for heart disease. In: Kamkin A, Kiseleva I, editors. Mechanosensitivity of the heart. Mechanosensitivity in cells and tissues: Springer Netherlands. 2010. p. 55–81.Google Scholar
- Anwar MA, Shalhoub J, Lim CS, Gohel MS, Davies AH. The effect of pressure-induced mechanical stretch on vascular wall differential gene expression. J Vasc Res. 2012;49(6):463–78. doi:https://doi.org/10.1159/000339151.View ArticlePubMedGoogle Scholar
- Chiu JJ, Usami S, Chien S. Vascular endothelial responses to altered shear stress: pathologic implications for atherosclerosis. Ann Med. 2009;41(1):19–28. doi:https://doi.org/10.1080/07853890802186921.View ArticlePubMedGoogle Scholar
- Ngai CY, Yao X. Vascular responses to shear stress: the involvement of mechanosensors in endothelial cells. Open Circ Vasc J. 2010;3:85–94.View ArticleGoogle Scholar
- Shyu KG. Cellular and molecular effects of mechanical stretch on vascular cells and cardiac myocytes. Clin Sci (Lond). 2009;116(5):377–89. doi:https://doi.org/10.1042/cs20080163.View ArticleGoogle Scholar
- Lacolley P. Mechanical influence of cyclic stretch on vascular endothelial cells. Cardiovasc Res. 2004;63(4):577–9. doi:https://doi.org/10.1016/j.cardiores.2004.06.017.View ArticlePubMedGoogle Scholar
- Thodeti CK, Matthews B, Ravi A, Mammoto A, Ghosh K, Bracha AL, et al. TRPV4 channels mediate cyclic strain-induced endothelial cell reorientation through integrin-to-integrin signaling. Circ Res. 2009;104(9):1123–30. doi:https://doi.org/10.1161/circresaha.108.192930.PubMed CentralView ArticlePubMedGoogle Scholar
- Naruse K, Yamada T, Sokabe M. Involvement of SA channels in orienting response of cultured endothelial cells to cyclic stretch. Am J Physiol. 1998;274(5 Pt 2):H1532–8.PubMedGoogle Scholar
- Adapala RK, Talasila PK, Bratz IN, Zhang DX, Suzuki M, Meszaros JG, et al. PKCalpha mediates acetylcholine-induced activation of TRPV4-dependent calcium influx in endothelial cells. Am J Physiol Heart Circ Physiol. 2011;301(3):H757–65. doi:https://doi.org/10.1152/ajpheart.00142.2011.PubMed CentralView ArticlePubMedGoogle Scholar
- Berrout J, Jin M, O’Neil RG. Critical role of TRPP2 and TRPC1 channels in stretch-induced injury of blood–brain barrier endothelial cells. Brain Res. 2012;1436:1–12. doi:https://doi.org/10.1016/j.brainres.2011.11.044.View ArticlePubMedGoogle Scholar
- Suzuki M, Naruse K, Asano Y, Okamoto T, Nishikimi N, Sakurai T, et al. Up-regulation of integrin beta 3 expression by cyclic stretch in human umbilical endothelial cells. Biochem Biophys Res Commun. 1997;239(2):372–6. doi:https://doi.org/10.1006/bbrc.1997.7364.View ArticlePubMedGoogle Scholar
- Katsumi A, Naoe T, Matsushita T, Kaibuchi K, Schwartz MA. Integrin activation and matrix binding mediate cellular responses to mechanical stretch. J Biol Chem. 2005;280(17):16546–9. doi:https://doi.org/10.1074/jbc.C400455200.View ArticlePubMedGoogle Scholar
- Zebda N, Dubrovskyi O, Birukov KG. Focal adhesion kinase regulation of mechanotransduction and its impact on endothelial cell functions. Microvas Res. 2012;83(1):71–81. doi:https://doi.org/10.1016/j.mvr.2011.06.007.View ArticleGoogle Scholar
- Katanosaka Y, Bao JH, Komatsu T, Suemori T, Yamada A, Mohri S, et al. Analysis of cyclic-stretching responses using cell-adhesion-patterned cells. J Biotechnol. 2008;133(1):82–9. doi:https://doi.org/10.1016/j.jbiotec.2007.09.017.View ArticlePubMedGoogle Scholar
- Osawa M, Masuda M, Kusano K-i, Fujiwara K. Evidence for a role of platelet endothelial cell adhesion molecule-1 in endothelial cell mechanosignal transduction: is it a mechanoresponsive molecule? J Cell Biol. 2002;158:773–85. doi:https://doi.org/10.1083/jcb.200205049.PubMed CentralView ArticlePubMedGoogle Scholar
- Ikeda M, Kito H, Sumpio BE. Phosphatidylinositol-3 kinase dependent MAP kinase activation via p21ras in endothelial cells exposed to cyclic strain. Biochem Biophys Res Commun. 1999;257(3):668–71. doi:https://doi.org/10.1006/bbrc.1999.0532.View ArticlePubMedGoogle Scholar
- Shi F, Chiu YJ, Cho Y, Bullard TA, Sokabe M, Fujiwara K. Down-regulation of ERK but not MEK phosphorylation in cultured endothelial cells by repeated changes in cyclic stretch. Cardiovas Res. 2007;73(4):813–22. doi:https://doi.org/10.1016/j.cardiores.2006.12.014.View ArticleGoogle Scholar
- Fujiwara K. Mechanical stresses keep endothelial cells healthy: beneficial effects of a physiological level of cyclic stretch on endothelial barrier function. Am J Physiol Lung Cell M Physiol. 2003;285(4):L782–4. doi:https://doi.org/10.1152/ajplung.00142.2003.View ArticleGoogle Scholar
- Ueki Y, Sakamoto N, Ohashi T, Sato M. Morphological responses of vascular endothelial cells induced by local stretch transmitted through intercellular junctions. Exp Mech. 2009;49(1):125–34. doi:https://doi.org/10.1007/s11340-008-9143-3.View ArticleGoogle Scholar
- Tojkander S, Gateva G, Lappalainen P. Actin stress fibers–assembly, dynamics and biological roles. J Cell Sci. 2012;125(Pt 8):1855–64. doi:https://doi.org/10.1242/jcs.098087.View ArticlePubMedGoogle Scholar
- Takemasa T, Yamaguchi T, Yamamoto Y, Sugimoto K, Yamashita K. Oblique alignment of stress fibers in cells reduces the mechanical stress in cyclically deforming fields. Eur J Cell Biol. 1998;77(2):91–9. doi:https://doi.org/10.1016/s0171-9335(98)80076-9.View ArticlePubMedGoogle Scholar
- Yoshigi M, Hoffman LM, Jensen CC, Yost HJ, Beckerle MC. Mechanical force mobilizes zyxin from focal adhesions to actin filaments and regulates cytoskeletal reinforcement. J C Biol. 2005;171(2):209–15. doi:https://doi.org/10.1083/jcb.200505018.View ArticleGoogle Scholar
- Yoshigi M, Clark EB, Yost HJ. Quantification of stretch-induced cytoskeletal remodeling in vascular endothelial cells by image processing. Cytometry A. 2003;55(2):109–18. doi:https://doi.org/10.1002/cyto.a.10076.View ArticlePubMedGoogle Scholar
- Huang W, Sakamoto N, Miyazawa R, Sato M. Role of paxillin in the early phase of orientation of the vascular endothelial cells exposed to cyclic stretching. Biochem Biophys Res Commun. 2012;418(4):708–13. doi:https://doi.org/10.1016/j.bbrc.2012.01.083.View ArticlePubMedGoogle Scholar
- Moretti M, Prina-Mello A, Reid AJ, Barron V, Prendergast PJ. Endothelial cell alignment on cyclically-stretched silicone surfaces. J Mater Sci Mater Med. 2004;15(10):1159–64. doi:https://doi.org/10.1023/b%3Ajmsm.0000046400.18607.72.View ArticlePubMedGoogle Scholar
- Barron V, Brougham C, Coghlan K, McLucas E, O’Mahoney D, Stenson-Cox C, et al. The effect of physiological cyclic stretch on the cell morphology, cell orientation and protein expression of endothelial cells. J Mater Sci Mater Med. 2007;18(10):1973–81. doi:https://doi.org/10.1007/s10856-007-3125-3.View ArticlePubMedGoogle Scholar
- Chien S. Mechanotransduction and endothelial cell homeostasis: the wisdom of the cell. Am J Physiol Heart Circ Physiol. 2007;292(3):H1209–24. doi:https://doi.org/10.1152/ajpheart.01047.2006.View ArticlePubMedGoogle Scholar
- Wang JH, Goldschmidt-Clermont P, Wille J, Yin FC. Specificity of endothelial cell reorientation in response to cyclic mechanical stretching. J Biomech. 2001;34(12):1563–72.View ArticlePubMedGoogle Scholar
- Kaunas R, Nguyen P, Usami S, Chien S. Cooperative effects of Rho and mechanical stretch on stress fiber organization. Proc Natl Acad Sci U S A. 2005;102(44):15895–900. doi:https://doi.org/10.1073/pnas.0506041102.PubMed CentralView ArticlePubMedGoogle Scholar
- Kaunas R, Usami S, Chien S. Regulation of stretch-induced JNK activation by stress fiber orientation. Cell Signal. 2006;18(11):1924–31. doi:https://doi.org/10.1016/j.cellsig.2006.02.008.View ArticlePubMedGoogle Scholar
- Hsu HJ, Lee CF, Locke A, Vanderzyl SQ, Kaunas R. Stretch-induced stress fiber remodeling and the activations of JNK and ERK depend on mechanical strain rate, but not FAK. PLoS One. 2010;5(8):e12470. doi:https://doi.org/10.1371/journal.pone.0012470.PubMed CentralView ArticlePubMedGoogle Scholar
- Luo SS, Sugimoto K, Fujii S, Takemasa T, Fu SB, Yamashita K. Role of heat shock protein 70 in induction of stress fiber formation in rat arterial endothelial cells in response to stretch stress. Acta Histochem Cytochem. 2007;40(1):9–17. doi:https://doi.org/10.1267/ahc.06011.PubMed CentralView ArticlePubMedGoogle Scholar
- Wang JH, Thampatty BP. An introductory review of cell mechanobiology. Biomech Model Mechanobiol. 2006;5(1):1–16. doi:https://doi.org/10.1007/s10237-005-0012-z.View ArticlePubMedGoogle Scholar
- Mekkawy AH, Pourgholami MH, Morris DL. Involvement of urokinase-type plasminogen activator system in cancer: an overview. Med Res Rev. 2014;34(5):918–56. doi:https://doi.org/10.1002/med.21308.View ArticlePubMedGoogle Scholar
- Loftus IM, Thompson MM. The role of matrix metalloproteinases in vascular disease. Vasc Med. 2002;7(2):117–33. doi:https://doi.org/10.1191/1358863x02vm420ra
- Rundhaug JE. Matrix metalloproteinases and angiogenesis. J Cell Mol Med. 2005;9(2):267–85.View ArticlePubMedGoogle Scholar
- von Offenberg SN, Cummins PM, Birney YA, Cullen JP, Redmond EM, Cahill PA. Cyclic strain-mediated regulation of endothelial matrix metalloproteinase-2 expression and activity. Cardiovasc Res. 2004;63(4):625–34. doi:https://doi.org/10.1016/j.cardiores.2004.05.008.View ArticleGoogle Scholar
- Wang B-W, Chang H, Lin S, Kuan P, Shyu K-G. Induction of matrix metalloproteinases-14 and −2 by cyclical mechanical stretch is mediated by tumor necrosis factor-alpha in cultured human umbilical vein endothelial cells. Cardiovasc Res. 2003;59:460–9.View ArticlePubMedGoogle Scholar
- Liu X-m L, Ensenat D, Wang H, Schafer AI, Durante W. Physiologic cyclic stretch inhibits apoptosis in vascular endothelium. FEBS Lett. 2003;541:52–6. doi:https://doi.org/10.1016/S0014-5793(03)00285-0.View ArticlePubMedGoogle Scholar
- Agewall S. Matrix metalloproteinases and cardiovascular disease. Eur Heart J. 2006;27:121–2. doi:https://doi.org/10.1093/eurheartj/ehi639.View ArticlePubMedGoogle Scholar
- Zheng W, Christensen LP, Tomanek RJ. Stretch induces upregulation of key tyrosine kinase receptors in microvascular endothelial cells. Am J Physiol Heart Circl Physiol. 2004;52242:2739–45. doi:https://doi.org/10.1152/ajpheart.00410.2004.View ArticleGoogle Scholar
- Zheng W, Christensen LP, Tomanek RJ. Differential effects of cyclic and static stretch on coronary microvascular endothelial cell receptors and vasculogenic / angiogenic responses. Am J Physiol Heart Circl Physiol. 2008;52242:794–800. doi:https://doi.org/10.1152/ajpheart.00343.2008.View ArticleGoogle Scholar
- Bocci G, Fasciani A, Danesi R, Viacava P, Genazzani AR, Del Tacca M. In-vitro evidence of autocrine secretion of vascular endothelial growth factor by endothelial cells from human placental blood vessels. Mol Hum Reprod. 2001;7(8):771–7.View ArticlePubMedGoogle Scholar
- Wang C, Jiao C, Hanlon HD, Zheng W, Tomanek RJ, Schatteman GC. Mechanical, cellular, and molecular factors interact to modulate circulating endothelial cell progenitors. Am J Physiol Heart Circl Physiol. 2004;286(5):H1985–93. doi:https://doi.org/10.1152/ajpheart.00431.2003.View ArticleGoogle Scholar
- Zheng W, Seftor EA, Meininger CJ, Hendrix MJ, Tomanek RJ. Mechanisms of coronary angiogenesis in response to stretch: role of VEGF and TGF-beta. Am J Physiol Heart Circl Physiol. 2001;280(2):H909–17.Google Scholar
- Wilkins JR, Pike DB, Gibson CC, Kubota A, Shiu YT. Differential effects of cyclic stretch on bFGF- and VEGF-induced sprouting angiogenesis. Biotechnol Prog. 2014;30(4):879–88. doi:https://doi.org/10.1002/btpr.1883.View ArticlePubMedGoogle Scholar
- Bao P, Kodra A, Tomic-Canic M, Golinko MS, Ehrlich HP, Brem H. The role of vascular endothelial growth factor in wound healing. J Surg Res. 2009;153(2):347–58. doi:https://doi.org/10.1016/j.jss.2008.04.023.PubMed CentralView ArticlePubMedGoogle Scholar
- Yung YC, Chae J, Buehler MJ, Hunter CP, Mooney DJ. Cyclic tensile strain triggers a sequence of autocrine and paracrine signaling to regulate angiogenic sprouting in human vascular cells. Proc Natl Acad Sci U S A. 2009;106:15279–84. doi:https://doi.org/10.1073/pnas.0905891106.PubMed CentralView ArticlePubMedGoogle Scholar
- Von Offenberg SN, Cummins PM, Cotter EJ, Fitzpatrick PA, Birney YA, Redmond EM, et al. Cyclic strain-mediated regulation of vascular endothelial cell migration and tube formation. Biochem Biophys Res Commun. 2005;329(2):573–82. doi:https://doi.org/10.1016/j.bbrc.2005.02.013.View ArticleGoogle Scholar
- Liu WF, Nelson CM, Tan JL, Chen CS. Cadherins, RhoA, and Rac1 are differentially required for stretch-mediated proliferation in endothelial versus smooth muscle cells. Circ Res. 2007;101:44–52. doi:https://doi.org/10.1161/CIRCRESAHA.107.158329.View ArticleGoogle Scholar
- Hurley NE, Schildmeyer LA, Bosworth KA, Sakurai Y, Eskin SG, Hurley LH, et al. Modulating the functional contributions of c-Myc to the human endothelial cell cyclic strain response. J Vasc Res. 2010;47:80–90. doi:https://doi.org/10.1159/000235928.PubMed CentralView ArticlePubMedGoogle Scholar
- Zhang K, Cao J, Dong R, Du J. Early growth response protein 1 promotes restenosis by upregulating intercellular adhesion molecule-1 in vein graft. Oxid Med Cell Longev. 2013;2013:1–9. doi:https://doi.org/10.1155/2013/432409.Google Scholar
- Michaelis UR, Fleming I. From endothelium-derived hyperpolarizing factor (EDHF) to angiogenesis: Epoxyeicosatrienoic acids (EETs) and cell signaling. Pharmacol Ther. 2006;111(3):584–95. doi:https://doi.org/10.1016/j.pharmthera.2005.11.003.View ArticlePubMedGoogle Scholar
- Cifarelli V, Lee S, Kim DH, Zhang T, Kamagate A, Slusher S, et al. FOXO1 mediates the autocrine effect of endothelin-1 on endothelial cell survival. Mol Endocrinol. 2012;26(7):1213–24. doi:https://doi.org/10.1210/me.2011-1276.PubMed CentralView ArticlePubMedGoogle Scholar
- Thacher TN, Silacci P, Stergiopulos N, da Silva RF. Autonomous effects of shear stress and cyclic circumferential stretch regarding endothelial dysfunction and oxidative stress: an ex vivo arterial model. J Vasc Res. 2010;47(4):336–45. doi:https://doi.org/10.1159/000265567.View ArticlePubMedGoogle Scholar
- Takeda H, Komori K, Nishikimi N, Nimura Y, Sokabe M, Naruse K. Bi-phasic activation of eNOS in response to uni-axial cyclic stretch is mediated by differential mechanisms in BAECs. Life Sci. 2006;79(3):233–9. doi:https://doi.org/10.1016/j.lfs.2005.12.051.View ArticlePubMedGoogle Scholar
- Fisslthaler B, Popp R, Michaelis UR, Kiss L, Fleming I, Busse R. Cyclic stretch enhances the expression and activity of coronary endothelium-derived hyperpolarizing factor synthase. Hypertension. 2001;38(6):1427–32. doi:https://doi.org/10.1161/hy1201.096532.
- Toda M, Yamamoto K, Shimizu N, Obi S, Kumagaya S, Igarashi T, et al. Differential gene responses in endothelial cells exposed to a combination of shear stress and cyclic stretch. J Biotechnol. 2008;133:239–44. doi:https://doi.org/10.1016/j.jbiotec.2007.08.009.View ArticlePubMedGoogle Scholar
- Koller A. Signaling pathways of mechanotransduction in arteriolar endothelium and smooth muscle cells in hypertension. Microcirculation. 2002;9:277–94. doi:https://doi.org/10.1038/sj.mn/7800142.View ArticlePubMedGoogle Scholar
- Ali MH, Mungai PT, Schumacker PT, Mir H, Stretch- PTS. Stretch-induced phosphorylation of focal adhesion kinase in endothelial cells : role of mitochondrial oxidants. Am J Physiol Heart Circl Physiol. 2006;60611:38–45. doi:https://doi.org/10.1152/ajplung.00287.2004.Google Scholar
- Goettsch C, Goettsch W, Arsov A, Hofbauer LC, Bornstein SR, Morawietz H. Long-term cyclic strain downregulates endothelial Nox4. Antioxid Redox Signal. 2009;11:2385–97. doi:https://doi.org/10.1089/ARS.2009.2561.View ArticlePubMedGoogle Scholar
- Ali MH, Pearlstein DP, Mathieu CE, Schumacker PT. Mitochondrial requirement for endothelial responses to cyclic strain: implications for mechanotransduction. Am J Physiol Lung Cell Mol Physiol. 2004;287:486–96. doi:https://doi.org/10.1152/ajplung.00389.2003.View ArticleGoogle Scholar
- Ross R. Atherosclerosis-an inflammatory disease. N Engl J Med. 1999;340:115–26.View ArticlePubMedGoogle Scholar
- Spescha RD, Glanzmann M, Simic B, Witassek F, Keller S, Akhmedov A, et al. Adaptor protein p66Shc mediates hypertension-associated, cyclic stretch-dependent, endothelial damage. Hypertension. 2014;64:347–53. doi:https://doi.org/10.1161/HYPERTENSIONAHA.113.02129.View ArticlePubMedGoogle Scholar
- Wagner AH, Kautz O, Fricke K, Zerr-Fouineau M, Demicheva E, Güldenzoph B, et al. Upregulation of glutathione peroxidase offsets stretch-induced proatherogenic gene expression in human endothelial cells. Arterioscler Thromb Vasc Biol. 2009;29:1894–901. doi:https://doi.org/10.1161/ATVBAHA.109.194738.View ArticlePubMedGoogle Scholar
- Balligand JL, Feron O, Dessy C. eNOS activation by physical forces: from short-term regulation of contraction to chronic remodeling of cardiovascular tissues. Physiol Rev. 2009;89(2):481–534. doi:https://doi.org/10.1152/physrev.00042.2007.View ArticlePubMedGoogle Scholar
- Frye SR, Yee A, Eskin SG, Guerra R, Cong X, McIntire LV. cDNA microarray analysis of endothelial cells subjected to cyclic mechanical strain: importance of motion control. Physiol Genomics. 2005;21(1):124–30. doi:https://doi.org/10.1152/physiolgenomics.00029.2003.View ArticlePubMedGoogle Scholar
- Xiong Y, Hu Z, Han X, Jiang B, Zhang R, Zhang X, et al. Hypertensive stretch regulates endothelial exocytosis of Weibel-Palade bodies through VEGF receptor 2 signaling pathways. Cell Res. 2013;23:820–34. doi:https://doi.org/10.1038/cr.2013.56.PubMed CentralView ArticlePubMedGoogle Scholar
- Kobayashi S, Nagino M, Komatsu S, Naruse K, Nimura Y, Nakanishi M, et al. Stretch-induced IL-6 secretion from endothelial cells requires NF-κB activation. Biochem Biophys Res Commun. 2003;308:306–12. doi:https://doi.org/10.1016/S0006-291X(03)01362-7.View ArticlePubMedGoogle Scholar
- Korff T, Aufgebauer K, Hecker M. Cyclic stretch controls the expression of CD40 in endothelial cells by changing their transforming growth factor-beta1 response. Circulation. 2007;116:2288–97. doi:https://doi.org/10.1161/CIRCULATIONAHA.107.730309.View ArticlePubMedGoogle Scholar
- Kou B, Zhang J, Singer DRJ. Effects of cyclic strain on endothelial cell apoptosis and tubulogenesis are dependent on ROS production via NAD(P)H subunit p22phox. Microvasc Res. 2009;77:125–33. doi:https://doi.org/10.1016/j.mvr.2008.08.001.View ArticlePubMedGoogle Scholar
- Nishimura K, Li W, Hoshino Y, Kadohama T, Asada H, Ohgi S, et al. Role of AKT in cyclic strain-induced endothelial cell proliferation and survival. Am J Physiol Cell Physiol. 2006;8062:812–21. doi:https://doi.org/10.1152/ajpcell.00347.2005.Google Scholar
- Lemarie CA, Tharaux PL, Lehoux S. Extracellular matrix alterations in hypertensive vascular remodeling. J Mol Cell Cardiol. 2010;48(3):433–9. doi:https://doi.org/10.1016/j.yjmcc.2009.09.018.View ArticlePubMedGoogle Scholar
- Okada M, Matsumori A, Ono K, Furukawa Y, Shioi T, Iwasaki A, et al. Cyclic stretch upregulates production of interleukin-8 and monocyte chemotactic and activating factor/monocyte chemoattractant protein-1 in human endothelial cells. Arterioscler Thromb Vasc Biol. 1998;18(6):894–901. doi:https://doi.org/10.1161/01.ATV.18.6.894
- Lee YU, Hayman D, Sprague EA, Han HC. Effects of axial stretch on cell proliferation and intimal thickness in arteries in organ culture. Cell Mol Bioeng. 2010;3(3):286–95. doi:https://doi.org/10.1007/s12195-010-0128-9.PubMed CentralView ArticlePubMedGoogle Scholar
- Hatami J, Tafazzoli-Shadpour M, Haghighipour N, Shokrgozar MA, Janmaleki M. Influence of cyclic stretch on mechanical properties of endothelial cells. Exp Mech. 2013;53(8):1291–8. doi:https://doi.org/10.1007/s11340-013-9744-3.View ArticleGoogle Scholar
- Cevallos M, Riha GM, Wang X, Yang H, Yan S, Li M, et al. Cyclic strain induces expression of specific smooth muscle cell markers in human endothelial cells. Differentiation. 2006;74(9–10):552–61. doi:https://doi.org/10.1111/j.1432-0436.2006.00089.x.View ArticlePubMedGoogle Scholar
- Shoajei S, Tafazzoli-Shahdpour M, Shokrgozar MA, Haghighipour N. Alteration of human umbilical vein endothelial cell gene expression in different biomechanical environments. Cell Biol Int. 2014;38(5):577–81. doi:https://doi.org/10.1002/cbin.10237.View ArticlePubMedGoogle Scholar
- Montezano AC, Touyz RM. Reactive oxygen species and endothelial function–role of nitric oxide synthase uncoupling and Nox family nicotinamide adenine dinucleotide phosphate oxidases. Basic Clin Pharmacol Toxicol. 2012;110(1):87–94. doi:https://doi.org/10.1111/j.1742-7843.2011.00785.x.View ArticlePubMedGoogle Scholar
- Dangas G. Restenosis: repeat narrowing of a coronary artery: prevention and treatment. Circulation. 2002;105(22):2586–87. doi:https://doi.org/10.1161/01.CIR.0000019122.00032.DF.
- Stula M, Orzechowski HD, Gschwend S, Vetter R, von Harsdorf R, Dietz R, et al. Influence of sustained mechanical stress on Egr-1 mRNA expression in cultured human endothelial cells. Mol Cell Biochem. 2000;210(1–2):101–8.View ArticlePubMedGoogle Scholar
- Juvela S. Prevalence of and risk factors for intracranial aneurysms. Lancet Neurol. 2011;10(7):595–7. doi:https://doi.org/10.1016/s1474-4422(11)70125-9.View ArticlePubMedGoogle Scholar
- Rinkel GJ, Djibuti M, Algra A, van Gijn J. Prevalence and risk of rupture of intracranial aneurysms: a systematic review. Stroke. 1998;29(1):251–6. doi:https://doi.org/10.1161/01.STR.29.1.251.
- Linn FH, Rinkel GJ, Algra A, van Gijn J. Incidence of subarachnoid hemorrhage: role of region, year, and rate of computed tomography: a meta-analysis. Stroke. 1996;27(4):625–9.View ArticlePubMedGoogle Scholar
- Fox B, Humphries WE, Doss VT, Hoit D, Elijovich L, Arthur AS. Rupture of giant vertebrobasilar aneurysm following flow diversion: mechanical stretch as a potential mechanism for early aneurysm rupture. J Neurointerv Surg. 2014;00:1-4. doi:https://doi.org/10.1136/bcr-2014-011325.
- Shikata Y, Rios A, Kawkitinarong K, DePaola N, Garcia JG, Birukov KG. Differential effects of shear stress and cyclic stretch on focal adhesion remodeling, site-specific FAK phosphorylation, and small GTPases in human lung endothelial cells. Exp Cell Res. 2005;304(1):40–9. doi:https://doi.org/10.1016/j.yexcr.2004.11.001.View ArticlePubMedGoogle Scholar
- Owatverot TB, Oswald SJ, Chen Y, Wille JJ, Yin FC. Effect of combined cyclic stretch and fluid shear stress on endothelial cell morphological responses. J Biomech Eng. 2005;127(3):374–82. doi:https://doi.org/10.1115/1.1894180.
- Haghighipour N, Tafazzoli-Shadpour M, Shokrgozar MA, Amini S. Effects of cyclic stretch waveform on endothelial cell morphology using fractal analysis. Artif Organs. 2010;34(6):481–90. doi:https://doi.org/10.1111/j.1525-1594.2010.01003.x.View ArticlePubMedGoogle Scholar
- Wang J, Lu D, Mao D, Long M. Mechanomics: an emerging field between biology and biomechanics. Protein Cell. 2014;5(7):518–31. doi:https://doi.org/10.1007/s13238-014-0057-9.PubMed CentralView ArticlePubMedGoogle Scholar
- Yamada T, Naruse K, Sokabe M. Stretch-induced morphological changes of human endothelial cells depend on the intracellular level of Ca2+ rather than of cAMP. Life Sci. 2000;67:2605–13.Google Scholar
- Naruse K, Sai X, Yokoyama N, Sokabe M. Uni-axial cyclic stretch induces c-src activation and translocation in human endothelial cells via SA channel activation. FEBS Lett. 1998;441:111–5.View ArticlePubMedGoogle Scholar
- Naruse K, Yamada T, Sai X, Hamaguchi M, Sokabe M. Pp125 FAK is required for stretch dependent morphological response of endothelial cells. Oncogene. 1998;17:455–63.View ArticlePubMedGoogle Scholar
- Shukla a, Dunn aR, Moses Ma, Van Vliet KJ. Endothelial cells as mechanical transducers: enzymatic activity and network formation under cyclic strain. Mech Chem Biosyst. 2004;1:279–90.Google Scholar
- Demicheva E, Hecker M, Korff T. Stretch-induced activation of the transcription factor activator protein-1 controls monocyte chemoattractant protein-1 expression during arteriogenesis. Circ Res. 2008;103:477–84. doi:https://doi.org/10.1161/CIRCRESAHA.108.177782.
- Zhao H, Hiroi T, Hansen BS, Rade JJ. Cyclic stretch induces cyclooxygenase-2 gene expression in vascular endothelial cells via activation of nuclear factor kappa-beta. Biochem Biophys Res Commun. 2009;389:599–601. doi:https://doi.org/10.1016/j.bbrc.2009.09.028.
- Wung BS, Cheng JJ, Shyue S-K, Wang DL. NO modulates monocyte chemotactic protein-1 expression in endothelial cells under cyclic strain. Arterioscler Thromb Vasc Biol. 2001;21:1941–47. doi:https://doi.org/10.1161/hq1201.099428.