Maturation of cell-substratum focal adhesions induced by depolymerization of microtubules is mediated by increased cortical tension.

O J Pletjushkina, A M Belkin, O J Ivanova, T Oliver, J M Vasiliev, K Jacobson
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引用次数: 44

Abstract

Dynamics of alterations of focal adhesions (FA) induced by a microtubule-depolymerizing drug, colcemid, was examined in several types of fibroblastic cells. Evolution of individual FA in cultured cells was monitored by interference-reflection microscopy (IRM); at the end of the monitoring period (3 hours) the cells were fixed and immunofluorescence microscopy of the same FA was performed with an antibody against vinculin. Control and colcemid-treated cells remained non-motile and did not show lamellipodial activity at the edges. During the incubation, formation of new FA or disappearance of pre-existing FA did not occur in either colcemid-treated or control cultures. However, FA in colcemid-treated cells significantly increased in size in the course of a 3 hour incubation. The growth of FA was centripetal and sometimes was accompanied by the fusion of several adjacent FA. Immunofluorescence examination showed that colcemid-induced growth of FA was accompanied by accumulation of several proteins specific for these structures including vinculin, talin, paxillin and pp125FAK kinase. Immunoblotting with anti-vinculin antibody showed that incubation with colcemid considerably increased the amount of vinculin associated with the ventral membranes due to its partial redistribution from a soluble pool into the growing adhesions. A substantial increase in tyrosine phosphorylation of pp125FAK was also observed in colcemid-treated cells. In cells plated on elastic silicone rubber films, colcemid induced formation of wrinkles in the films and these wrinkles relaxed after treatment with cytochalasin D. These results confirm that microtubule depolymerization increases traction transmitted to the substratum by the actin cortex and shows that an increase in cortical tension accompanies maturation of FA. Taken together, these data show that short-term incubation with colcemid does not affect the formation of initial FA. In contrast, microtubule depolymerization considerably stimulates the maturation FA, manifested by their centripetal growth. Maturation is proposed to be mediated by increased cortical tension, which is caused by microtubule depolymerization.

微管解聚引起的细胞-基质局灶性粘连的成熟是由皮质张力增加介导的。
在几种类型的成纤维细胞中,研究了一种微管解聚药物,秋碱引起的局灶粘连(FA)改变的动力学。用干涉反射显微镜(IRM)观察培养细胞中单个FA的进化;在监测期结束时(3小时),将细胞固定,并对同一FA进行免疫荧光显微镜检查,并使用抗vinculin抗体。对照和秋碱处理的细胞保持不运动,边缘不显示板足活性。在培养过程中,无论是用秋碱处理还是对照培养,都没有出现新的FA的形成或原有FA的消失。然而,在3小时的孵育过程中,经colcolid处理的细胞FA的大小显著增加。FA向心生长,有时伴有相邻几个FA的融合。免疫荧光检测显示,秋碱诱导的FA生长伴随着几种特异性蛋白的积累,包括vinculin、talin、paxillin和pp125FAK激酶。抗毒蛋白抗体免疫斑点分析显示,用秋胶肽孵育可显著增加与腹侧膜相关的毒蛋白的数量,这是由于其部分从可溶性池重新分布到生长的黏附中。在经colcolide处理的细胞中,pp125FAK的酪氨酸磷酸化也显著增加。在弹性硅橡胶薄膜上的细胞中,秋碱诱导薄膜上的皱纹形成,这些皱纹在细胞松弛素d处理后松弛。这些结果证实微管解聚增加了肌动蛋白皮层传递给基质的牵引力,并表明皮质张力的增加伴随着FA的成熟。综上所述,这些数据表明,短期用秋碱孵育不影响初始FA的形成。相反,微管解聚极大地刺激了FA的成熟,表现为它们的向心生长。成熟被认为是由微管解聚引起的皮质张力增加介导的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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