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首页> 外文期刊>Journal of Biomechanics >Effect of LIMK2 RNAi on reorganization of the actin cytoskeleton in osteoblasts induced by fluid shear stress.
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Effect of LIMK2 RNAi on reorganization of the actin cytoskeleton in osteoblasts induced by fluid shear stress.

机译:LIMK2 RNAi对流体剪切应力诱导的成骨细胞肌动蛋白细胞骨架重组的影响。

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The biomechanical characteristics of bone tissue and its cells under mechanical stress are significant for bone biomechanics research, but the mechanism of mechanotransduction is still unknown. It has been established that the actin cytoskeleton of osteoblasts plays an important role in this process. However, the structure of the actin cytoskeleton is reorganized when loaded with mechanical stress, which results in changes in cell stiffness. These phenomena suggest that an actin-cytoskeleton-induced feedback regulation mechanism may be involved in the mechanotransduction of osteoblasts, but this has not yet been proven. The aim of this study was to explore the role of LIMK2 in the reorganization of the actin cytoskeleton induced by fluid shear stress in osteoblasts by using RNA interference. Balb/c mouse primary osteoblasts were divided into four groups. Cells in Groups 1 and 3 were transfected with negative control RNA, while cells in Groups 2 and 4 were transfected with a specific siRNA designed to silence the LIMK2 gene. Twenty-four hours after transfection, cells in Groups 1 and 2 were loaded with fluid shear stress at 12 dyne/cm2 while cells in Groups 3 and 4 were not. Compared with Group 1, the mean fluorescence density of the actin cytoskeleton in the other three groups was 28.9%, 45.7%, and 33.0%, respectively. These results indicate that LIMK2 plays an important role in the reorganization of the actin cytoskeleton induced by fluid shear stress.
机译:骨组织及其细胞在机械应力作用下的生物力学特性对骨生物力学研究具有重要意义,但机械转导的机制尚不清楚。已经确定,成骨细胞的肌动蛋白细胞骨架在该过程中起重要作用。然而,肌动蛋白细胞骨架的结构在受到机械压力时会重新组织,这会导致细胞硬度的变化。这些现象表明肌动蛋白细胞骨架诱导的反馈调节机制可能参与成骨细胞的机械转导,但尚未得到证实。这项研究的目的是探讨利用RNA干扰,LIMK2在成骨细胞中的流体剪切应力诱导的肌动蛋白细胞骨架重组中的作用。 Balb / c小鼠原代成骨细胞分为四组。将第1和第3组的细胞用阴性对照RNA转染,而将第2和第4组的细胞用设计为沉默LIMK2基因的特异性siRNA转染。转染后二十四小时,第1和第2组的细胞以12达因/平方厘米的流体剪切应力加载,而第3和第4组的细胞则没有。与第1组相比,其他三组肌动蛋白细胞骨架的平均荧光密度分别为28.9%,45.7%和33.0%。这些结果表明LIMK2在由流体剪切应力诱导的肌动蛋白细胞骨架的重组中起重要作用。

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