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波形蛋白破坏对关节软骨细胞机械反应的影响。

Effects of vimentin disruption on the mechanoresponses of articular chondrocyte.

作者信息

Chen Cheng, Yin Li, Song Xiongbo, Yang Hao, Ren Xiang, Gong Xiaoyuan, Wang Fuyou, Yang Liu

机构信息

Center for Joint Surgery, Southwest Hospital, The Third Military Medical University, Chongqing 400038, PR China.

Center for Joint Surgery, Southwest Hospital, The Third Military Medical University, Chongqing 400038, PR China.

出版信息

Biochem Biophys Res Commun. 2016 Jan 1;469(1):132-137. doi: 10.1016/j.bbrc.2015.11.083. Epub 2015 Nov 23.

Abstract

Human articular cartilage is subjected to repetitive mechanical loading during life time. As the only cellular component of articular cartilage, chondrocytes play a key role in the mechanotransduction within this tissue. The mechanoresponses of chondrocytes are largely determined by the cytoskeleton. Vimentin intermediate filaments, one of the major cytoskeletal components, have been shown to regulate chondrocyte phenotype. However, the contribution of vimentin in chondrocyte mechanoresponses remains less studied. In this study, we seeded goat articular chondrocytes on a soft polyacrylamide gel, and disrupted the vimentin cytoskeleton using acrylamide. Then we applied a transient stretch or compression to the cells, and measured the changes of cellular stiffness and traction forces using Optical Magnetic Twisting Cytometry and Traction Force Microscopy, respectively. In addition, to study the effects of vimentin disruption on the intracellular force generation, we treated the cells with a variety of reagents that are known to increase or decrease cytoskeletal tension. We found that, after a compression, the contractile moment and cellular stiffness were not affected in untreated chondrocytes, but were decreased in vimentin-disrupted chondrocytes; after a stretch, vimentin-disrupted chondrocytes showed a lower level of fluidization-resolidification response compared to untreated cells. Moreover, vimentin-disrupted chondrocytes didn't show much difference to control cells in responding to reagents that target actin and ROCK pathway, but showed a weaker response to histamine and isoproterenol. These findings confirmed chondrocyte vimentin as a major contributor in withstanding compressive loading, and its minor role in regulating cytoskeletal tension.

摘要

人类关节软骨在生命周期中承受反复的机械负荷。作为关节软骨唯一的细胞成分,软骨细胞在该组织的机械转导中起关键作用。软骨细胞的机械反应在很大程度上由细胞骨架决定。波形蛋白中间丝是主要的细胞骨架成分之一,已被证明可调节软骨细胞表型。然而,波形蛋白在软骨细胞机械反应中的作用仍鲜少被研究。在本研究中,我们将山羊关节软骨细胞接种在柔软的聚丙烯酰胺凝胶上,并用丙烯酰胺破坏波形蛋白细胞骨架。然后我们对细胞施加短暂的拉伸或压缩,并分别使用光磁扭转细胞术和牵引力显微镜测量细胞硬度和牵引力的变化。此外,为了研究波形蛋白破坏对细胞内力产生的影响,我们用各种已知可增加或降低细胞骨架张力的试剂处理细胞。我们发现,压缩后,未处理的软骨细胞的收缩力矩和细胞硬度不受影响,但波形蛋白破坏的软骨细胞则降低;拉伸后,与未处理的细胞相比,波形蛋白破坏的软骨细胞表现出较低水平的流化 - 再固化反应。此外,波形蛋白破坏的软骨细胞在对靶向肌动蛋白和ROCK途径的试剂反应方面与对照细胞没有太大差异,但对组胺和异丙肾上腺素的反应较弱。这些发现证实软骨细胞波形蛋白是承受压缩负荷的主要因素,并且其在调节细胞骨架张力方面作用较小。

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