Department of Chemistry and Forensic Science, Savannah State University, Savannah, GA, 31404, USA.
Department of Chemistry and Forensic Science, Savannah State University, Savannah, GA, 31404, USA.
Biochem Biophys Res Commun. 2019 Jan 1;508(1):302-307. doi: 10.1016/j.bbrc.2018.11.142. Epub 2018 Nov 28.
Vinculin is a key player in sensing and responding to external mechanical cues such as extracellular matrix stiffness. Increased matrix stiffness is often associated with certain pathological conditions including hypertension induced cellular cytoskeleton changes in vascular smooth muscle (VSM) cells. However, little is known on how stiffness affects cytoskeletal remodeling via vinculin in VSM cells. Thus, we utilized matrices with elastic moduli that simulate vascular stiffness in different stages of hypertension to investigate how matrix stiffness regulates cell cytoskeleton via vinculin in synthetic VSM cells. Through selecting a suitable reference gene, we found that an increase in physiologically relevant extracellular matrix stiffness (2-50 kPa) downregulates vinculin gene expression but upregulates vinculin protein expression. This discrepancy, which was not observed previously for non-muscle cells, suggests that the vinculin-mediated mecahnotransduction mechanism in synthetic VSM cells may be more complex than those proposed for non-muscle cells. Also adding to previous findings, we found that VSM cell growth may be impeded by substrates that are either too soft or too rigid.
粘着斑蛋白是感知和响应外部机械线索(如细胞外基质硬度)的关键分子。细胞外基质硬度的增加通常与某些病理状况有关,包括高血压引起的血管平滑肌(VSM)细胞细胞骨架的变化。然而,对于硬度如何通过粘着斑蛋白影响 VSM 细胞中的细胞骨架重塑,我们知之甚少。因此,我们利用模拟高血压不同阶段血管硬度的弹性模量不同的基质来研究基质硬度如何通过粘着斑蛋白调节合成 VSM 细胞中的细胞骨架。通过选择合适的参考基因,我们发现生理相关的细胞外基质硬度(2-50 kPa)的增加下调了粘着斑蛋白基因的表达,但上调了粘着斑蛋白的表达。这种差异在非肌肉细胞中以前没有观察到,这表明粘着斑蛋白介导的机械转导机制在合成 VSM 细胞中可能比在非肌肉细胞中更为复杂。此外,与以前的发现一致的是,我们发现 VSM 细胞的生长可能会受到太软或太硬的基质的阻碍。