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细胞外基质的存在改变了软骨细胞对内质网应激的反应。

The presence of extracellular matrix alters the chondrocyte response to endoplasmic reticulum stress.

机构信息

Department of Anatomy and Neurobiology, Northeastern Ohio Universities Colleges of Medicine and Pharmacy, Rootstown, Ohio, USA.

出版信息

J Cell Biochem. 2011 Apr;112(4):1118-29. doi: 10.1002/jcb.23025.

Abstract

The objective of this study was to test the hypothesis that extracellular matrix (ECM) would alter the endoplasmic reticulum (ER) stress response of chondrocytes. Chondrocytes were isolated from calf knees and maintained in monolayer culture or suspended in collagen I to form spot cultures (SCs). Our laboratory has shown that bovine chondrocytes form cartilage with properties similar to native cartilage after 2-4 weeks in SCs. Monolayer cultures treated with ER stressors glucose withdrawal (-Glu), tunicamycin (TN), or thapsigargin (TG) up-regulated Grp78 and Gadd153, demonstrating a complete ER stress response. SCs were grown at specific times from 1 day to 6 weeks before treatment with ER stressors. Additionally, SCs grown for 1, 2, or 6 weeks were treated with increasing concentrations of TN or TG. Western blotting of SCs for Grp78 indicated that increased ECM accumulation results in delayed expression; however, Grp78 mRNA is up-regulated in response to ER stressors even after 6 weeks in culture. SCs treated with ER stressors did not up-regulate Gadd153, suggesting that the cells experienced ER stress but would not undergo apoptosis. In fact, SCs undergo apoptosis upon ER stress treatment after 0-1 day of growth; however, after 4 days and to 6 weeks, apoptosis in treated samples was not different than controls. Pro-survival molecules Bcl-2 and Bag-1 were up-regulated upon ER stress in SCs. These results suggest that presence of ECM confers protection from ER stressors. Future studies involving chondrocyte physiology should focus on responses in conditions more closely mimicking the in vivo cartilage environment.

摘要

本研究旨在验证以下假设

细胞外基质(ECM)会改变软骨细胞的内质网(ER)应激反应。从小牛膝盖中分离软骨细胞,并在单层培养或悬浮于 I 型胶原中形成点状培养物(SCs)中进行培养。本实验室已经证明,牛软骨细胞在 SC 中培养 2-4 周后可形成具有类似天然软骨特性的软骨。经葡萄糖剥夺(-Glu)、衣霉素(TN)或他普西隆(TG)等 ER 应激剂处理的单层培养物上调了 Grp78 和 Gadd153,表明其发生了完整的 ER 应激反应。SC 分别在培养 1 天至 6 周时开始用 ER 应激剂处理。此外,培养 1、2 或 6 周的 SC 用不同浓度的 TN 或 TG 处理。Grp78 的 SC 蛋白印迹表明,ECM 积累增加会导致表达延迟;然而,即使在培养 6 周后,Grp78 mRNA 仍会因 ER 应激剂而上调。用 ER 应激剂处理的 SC 并未上调 Gadd153,表明细胞经历了 ER 应激但不会发生细胞凋亡。实际上,SC 在培养 0-1 天后用 ER 应激剂处理时会发生细胞凋亡;但是,培养 4 天和 6 周后,处理组和对照组的凋亡没有差异。SC 中的生存促进分子 Bcl-2 和 Bag-1 在 ER 应激时上调。这些结果表明 ECM 的存在赋予了对 ER 应激剂的保护作用。未来涉及软骨细胞生理学的研究应集中在更接近模拟体内软骨环境的条件下的反应。

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