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Stimulation of regulatory volume decrease (RVD) by isolated bovine articular chondrocytes following F-actin disruption using latrunculin B

机译:F-肌动蛋白破坏后使用latrunculin B刺激分离的牛关节软骨细胞刺激调节体积减少(RVD)

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Articular chondrocytes are exposed to significant changes in extracellular osmolarity during normal joint activity, which can lead to changes in cell volume and metabolism of the extracellular matrix (ECM). Chondrocytes can respond to cell swelling/shrinking by volume regulatory pathways, but the signalling pathways are poorly understood although a role for the cytoskeleton is frequently implicated. Here, we have investigated the effects of disruption of the chondrocyte F-actin cytoskele-ton on the recovery of cell volume by RVD. The cytoskeleton was perturbed using the relatively specific agent latrunculin B (5 μM; 30 min) and loss of F-actin integrity quantified using fluorescent phalloidin-labelling and confocal laser scanning microscopy (CLSM). Imaging of isolated chondrocytes labelled with Fura-2 to measure the fluorescence associated with cell volume changes, showed that the extent of hypo-osmotic swelling was unaffected by latrunculin B treatment. Two categories of the chondrocyte RVD response were observed: 'fast' RVD where at 3 min post-osmotic challenge there was a recovery in cell fluorescence of ≥80%, whereas other cells exhibited 'slow' RVD. Latrunculin B increased the proportion of chondrocytes demonstrating 'fast' RVD by ~10 fold and reduced those cells showing 'slow' RVD. An inhibitor of chondrocyte RVD (REV 5901) had no significant effect on the integrity of the cytoskeleton showing that the RVD response could be inhibited independent of the state of the F-actin cytoskeleton. These results suggest that the intact cortical F-actin cytoskeleton has a restraining effect on the RVD response of isolated bovine articular chondrocytes.
机译:在正常关节活动期间,关节软骨细胞暴露于细胞外渗透压的显着变化,这可能导致细胞体积和细胞外基质(ECM)代谢的变化。软骨细胞可以通过体积调节途径对细胞肿胀/萎缩作出反应,但对信号传导途径的了解却很少,尽管经常涉及细胞骨架的作用。在这里,我们研究了软骨细胞F-肌动蛋白细胞骨架的破坏对RVD恢复细胞体积的影响。使用相对特异的试剂latrunculin B(5μM; 30分钟)扰动细胞骨架,并使用荧光鬼笔环肽标记和共聚焦激光扫描显微镜(CLSM)定量F-肌动蛋白完整性的丧失。对用Fura-2标记的分离的软骨细胞进行成像以测量与细胞体积变化相关的荧光,表明低渗溶胀程度不受latrunculin B处理的影响。观察到两种类型的软骨细胞RVD响应:“快速” RVD,在渗透后3分钟,细胞荧光恢复率≥80%,而其他细胞则显示“慢” RVD。 Latrunculin B使表现出“快速” RVD的软骨细胞比例增加了约10倍,并使显示“慢速” RVD的那些细胞减少。软骨细胞RVD抑制剂(REV 5901)对细胞骨架的完整性无明显影响,表明RVD反应可以不受F-肌动蛋白细胞骨架状态的抑制。这些结果表明完整的皮质F-肌动蛋白细胞骨架对分离的牛关节软骨细胞的RVD反应具有抑制作用。

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