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首页> 外文期刊>Journal of orthopaedic research >Leptin-mediated cytoskeletal remodeling in chondrocytes occurs via the RhoA/ROCK pathway.
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Leptin-mediated cytoskeletal remodeling in chondrocytes occurs via the RhoA/ROCK pathway.

机译:瘦素介导的软骨细胞重塑通过RhoA / ROCK途径发生。

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摘要

Leptin affects a number of cell signaling pathways, at present, the mechanism(s) by which leptin affects the cartilage cells in OA patient is not well understood. The current study seeks to elucidate whether leptin induces cytoskeletal remodeling in chondrocytes and the possible involvement of the RhoA/ROCK pathway and its downstream mediators in this process. Fluorescent resonance energy transfer (FRET) and western analysis were used to determine the activations of the key proteins in the RhoA/LIMK1/Cofilin pathway. Accompanying cytoskeletal remodeling was elucidated. Upon leptin stimulation, a substantial increase of RhoA activity localized at one end of the cell was observed from 2 to 30 min post-stimulation. The results of Western blot showed leptin significantly increased LIMK1 and cofilin-2 phosphorylation in a time-dependent manner with maximal stimulation attained 60 min and 24 h post-stimulation, respectively. Chondrocytes stimulated with leptin exhibited an epithelioid morphology with increased cellular spreading. F-actin in leptin-stimulated chondrocytes also showed more intense cytoplasmic staining with occasional localization along filamentous structures. The results indicate that leptin activates the RhoA/ROCK/LIMK/cofilin pathway, which results in cytoskeletal reorganization in chondrocytes. These findings provide novel evidence supporting the possible involvement of leptin and the RhoA pathway in the pathogenesis of OA.
机译:瘦素影响许多细胞信号传导途径,目前,瘦素影响OA患者的软骨细胞的机制尚不清楚。当前的研究试图阐明瘦素是否在软骨细胞中诱导细胞骨架重塑,以及RhoA / ROCK途径及其下游介质可能参与这一过程。荧光共振能量转移(FRET)和western分析用于确定RhoA / LIMK1 / Cofilin途径中关键蛋白的活化。阐明了伴随的细胞骨架重塑。瘦素刺激后,从刺激后2到30分钟观察到定位在细胞一端的RhoA活性显着增加。蛋白质印迹的结果表明,瘦素以时间依赖性方式显着增加LIMK1和cofilin-2磷酸化,最大刺激分别在刺激后60分钟和24小时达到。瘦素刺激的软骨细胞表现出上皮样形态,细胞扩散增加。瘦蛋白刺激的软骨细胞中的F-肌动蛋白还显示出更强烈的细胞质染色,偶有沿丝状结构的定位。结果表明瘦蛋白激活RhoA / ROCK / LIMK / cofilin途径,从而导致软骨细胞的细胞骨架重组。这些发现提供了新的证据,证明瘦素和RhoA途径可能与OA的发病有关。

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