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牛关节软骨细胞中丝裂原活化蛋白激酶信号传导对流体流动的响应不需要钙动员。

Mitogen-activated protein kinase signaling in bovine articular chondrocytes in response to fluid flow does not require calcium mobilization.

作者信息

Hung C T, Henshaw D R, Wang C C, Mauck R L, Raia F, Palmer G, Chao P H, Mow V C, Ratcliffe A, Valhmu W B

机构信息

Cellular Engineering Laboratory, Center for Biomedical Engineering, Columbia University, New York, NY 10027, USA.

出版信息

J Biomech. 2000 Jan;33(1):73-80. doi: 10.1016/s0021-9290(99)00176-1.

Abstract

In the present study, the role of mitogen-activated protein kinases (MAPKs) in chondrocyte mechanotransduction was investigated. We hypothesized that MAPKs participate in fluid flow-induced chondrocyte mechanotransduction. To test our hypothesis, we studied cultured chondrocytes subjected to a well-defined mechanical stimulus generated with a laminar flow chamber. The extracellular signal-regulated kinases 1 and 2 (ERK1/2) were activated 1.6-3-fold after 5-15 min of fluid flow exposure corresponding to a chamber wall shear stress of 1.6 Pa. Activation of ERK1/2 was observed in the presence of both 10% FBS and 0.1% BSA, suggesting that the flow effects do not require serum agonists. Treatment with thapsigargin or EGTA had no significant effect on the ERK1/2 activation response to flow, suggesting that Ca2+ mobilization is not required for this response. To assess downstream effects of the activated MAPKs on transcription, flow studies were performed using chondrocytes transfected with a chimeric luciferase construct containing 2.4 kb of the promoter region along with exon 1 of the human aggrecan gene. Two-hour exposure of transfected chondrocytes to fluid flow significantly decreased aggrecan promoter activity by 40%. This response was blocked by treatment of chondrocytes with the MEK-1 inhibitor PD98059. These findings demonstrate that, under the conditions of the present study, fluid flow-induced signals activate the MEK-1/ERK signaling pathway in articular chondrocytes, leading to down-regulation of expression of the aggrecan gene.

摘要

在本研究中,我们调查了丝裂原活化蛋白激酶(MAPKs)在软骨细胞机械转导中的作用。我们假设MAPKs参与流体流动诱导的软骨细胞机械转导。为了验证我们的假设,我们研究了培养的软骨细胞,这些细胞受到层流室产生的明确机械刺激。在对应于1.6 Pa室壁剪切应力的流体流动暴露5 - 15分钟后,细胞外信号调节激酶1和2(ERK1/2)被激活1.6 - 3倍。在同时存在10%胎牛血清(FBS)和0.1%牛血清白蛋白(BSA)的情况下观察到ERK1/2的激活,这表明流动效应不需要血清激动剂。用毒胡萝卜素或乙二醇双四乙酸(EGTA)处理对ERK1/2对流动的激活反应没有显著影响,这表明该反应不需要Ca2+动员。为了评估活化的MAPKs对转录的下游效应,使用转染了包含2.4 kb启动子区域以及人聚集蛋白聚糖基因外显子1的嵌合荧光素酶构建体的软骨细胞进行流动研究。转染的软骨细胞暴露于流体流动两小时后,聚集蛋白聚糖启动子活性显著降低了40%。用MEK - 1抑制剂PD98059处理软骨细胞可阻断此反应。这些发现表明,在本研究条件下,流体流动诱导的信号激活关节软骨细胞中的MEK - 1/ERK信号通路,导致聚集蛋白聚糖基因表达下调。

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