首页> 外文会议>Annual Northeast Bioengineering Conference >Interstitial Flow Induces MMP-1 Expression and SMC Migration in 3-D Collagen I Gels via an ERKl/2-c-Jun Pathway and Mechanosenation by Heparan Sulfate Proteoglycans and Focal Adhesions
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Interstitial Flow Induces MMP-1 Expression and SMC Migration in 3-D Collagen I Gels via an ERKl/2-c-Jun Pathway and Mechanosenation by Heparan Sulfate Proteoglycans and Focal Adhesions

机译:间质流量通过Erkl / 2-C-Jun途径和通过硫酸普肽蛋白多糖和局灶性粘连在3-D胶原蛋白I凝胶中诱导MMP-1表达和SMC迁移

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The migration of vascular smooth muscle cells (SMCs) and fibroblasts into the intima after vascular injury is a central process in vascular lesion formation. The elevation of transmural interstitial flow is also observed after damage to the vascular endothelium. We have previously shown that interstitial flow promotes vascular cell motility in 3-D collagen I gels via upregulation of MMP-1. In this work, we further reveal that interstitial flow-induced MMP-1 expression and cell migration proceeds through the ERKl/2-c-Jun pathway. We also show that heparin sulfate proteoglycans (HSPGs) and focal adhesion kinase (FAK) are sensors and transmitters which convert the interstitial flow stimulus to biomolecular responses and altered cell function (migration). Our findings suggest that interstitial flow shear stress may play an important role in migration of SMCs and fibroblasts during neointima formation and vascular remodeling.
机译:血管损伤后血管平滑肌细胞(SMC)和成纤维细胞的迁移为血管病变形成的中央方法。在对血管内皮损伤后,也观察到透息间流动的升高。我们以前表明,间质流动通过MMP-1的上调促进了3-D胶原I凝胶中的血管细胞运动。在这项工作中,我们进一步揭示了间质流动诱导的MMP-1表达和细胞迁移通过ERKL / 2-C-Jun路径进行。我们还表明,硫酸肝素蛋白多糖(HSPG)和局灶性粘附激酶(FAK)是转化为生物分子应答和改变细胞功能(迁移)的间质流量刺激的传感器和发射器。我们的研究结果表明,间质流量剪切应力可能在新内膜形成和血管重塑期间在SMC和成纤维细胞迁移中发挥重要作用。

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