Endothelial connexin 37, connexin 40, and connexin 43 respond uniquely to substrate and shear stress.

Tiffany L Johnson, Robert M Nerem
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引用次数: 51

Abstract

Endothelial connexins have been linked to atherosclerosis and hypertension; however, little is know about their sensitivity to stimuli and individual functions. This study investigates the responses of endothelial connexin 37, connexin 40, and connexin 43 (Cx37, Cx40, and Cx43) to shear stress and substrate. Human endothelial cells were seeded on adsorbed collagen or a collagen gel containing smooth muscle cells and exposed to static or laminar shear stress. Connexin mRNA, protein, and gap junction communication were examined. Endothelial monolayers were treated with connexin-specific short interfering RNA (siRNA) and evaluated for communication, proliferation, and morphology under static and shear stress. Results show differential responses of Cx37, Cx40, and Cx43 to substrate and shear stress with reduced communication after shear exposure. RNA interference of individual connexins resulted in expression change of nontarget connexins, which suggests linked expression. Gap junction communication under static conditions is reduced following Cx43 siRNA treatment. Endothelial cells are more elongated with RNA interference (RNAi) targeting Cx40. In conclusion, endothelial connexins demonstrated novel sensitivity to mechanical environment and substrate. Individual isotypes show differential responses and RNAi knockdown provides new insight into connexin function and potential roles in the vasculature.

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内皮连接蛋白 37、连接蛋白 40 和连接蛋白 43 对底物和剪切应力有独特的反应。
内皮连接蛋白与动脉粥样硬化和高血压有关;然而,人们对它们对刺激的敏感性和各自的功能知之甚少。本研究调查了内皮连接蛋白 37、连接蛋白 40 和连接蛋白 43(Cx37、Cx40 和 Cx43)对剪切应力和基质的反应。将人内皮细胞播种在吸附的胶原蛋白或含有平滑肌细胞的胶原凝胶上,并暴露在静态或层状剪切应力下。对连接蛋白 mRNA、蛋白质和缝隙连接通信进行了检测。用连接蛋白特异性短干扰 RNA(siRNA)处理内皮单层,并评估其在静态和剪切应力下的通讯、增殖和形态。结果显示,Cx37、Cx40 和 Cx43 对基质和剪切应力的反应不同,剪切暴露后的通讯减少。对单个连接蛋白的 RNA 干扰导致非目标连接蛋白的表达发生变化,这表明连接蛋白的表达是相互关联的。Cx43 siRNA 处理后,静态条件下的缝隙连接通讯减少。针对 Cx40 的 RNA 干扰(RNAi)会使内皮细胞更加伸长。总之,内皮连接蛋白对机械环境和基质表现出了新的敏感性。单个异型表现出不同的反应,而 RNAi 敲除则提供了对连接蛋白功能和在血管中潜在作用的新见解。
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