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Shear stress magnitude is critical in regulating the differentiation of mesenchymal stem cells even with endothelial growth medium

机译:剪切应力的大小对于调节间充质干细胞的分化至关重要,即使在内皮生长培养基中也是如此

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摘要

Human mesenchymal stem cells (MSC) were seeded onto the inner surface of a tubular silicon construct and, after 24 h, were exposed to a shearing stress of either 2.5 or 10 dyne/cm2 for 1 day. The fluid contained endothelial growth factors in both cases. Morphological changes and cytoskeletal rearrangements were observed in the stimulated cells. Immunofluorescence staining showed that low (2.5 dyne/cm2) and high shear stress (10 dyne/cm2) resulted in the expression of von Willebrand factor (vWF) and calponin, respectively. At low shear stress, CD31 (PECAM-1) was significantly expressed whereas vWF and KDR expression was only slightly higher than those under 10 dyne/cm2. All three markers related to smooth muscle cells (myocardin, myosin heavy chain, and SM‐22α) had significantly higher expression under shear stress of 10 dyne/cm2 compared with a 2.5 dyne/cm2, even in endothelial growth medium. Shear stress plays a critical role in regulating MSC differentiation and must be considered for bioengineered blood vessels.
机译:将人间充质干细胞(MSC)播种到管状硅构建体的内表面上,并在24小时后暴露于2.5或10达因/ cm 2 的剪切应力下1天。在两种情况下,液体均含有内皮生长因子。在刺激的细胞中观察到形态变化和细胞骨架重排。免疫荧光染色显示,低(2.5达因/ cm 2 )和高切应力(10达因/ cm 2 )导致血管性假血友病因子(vWF)和钙蛋白的表达, 分别。在低剪切应力下,CD31(PECAM-1)的表达明显,而vWF和KDR的表达仅略高于10达因/ cm 2 下的表达。在剪切应力为10达因/ cm 2 的情况下,与平滑肌细胞相关的所有三个标志物(心肌素,肌球蛋白重链和SM-22α)的表达均显着高于2.5达因/ cm 2 ,甚至在内皮生长培养基中也是如此。剪应力在调节MSC分化中起着关键作用,对于生物工程血管必须考虑。

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