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
Cellular Engineering Laboratory, Center for Biomedical Engineering, Columbia University, New York, NY 10027, USA.
J Biomech. 2000 Jan;33(1):73-80. doi: 10.1016/s0021-9290(99)00176-1.
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.
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。