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胞质动力蛋白参与间期细胞中微管在中心体的保留。

Cytoplasmic dynein is involved in the retention of microtubules at the centrosome in interphase cells.

作者信息

Burakov Anton, Kovalenko Olga, Semenova Irina, Zhapparova Olga, Nadezhdina Elena, Rodionov Vladimir

机构信息

Department of Cell Biology and Center for Cell Analysis and Modeling, University of Connecticut Health Center, 263 Farmington Avenue-MC1507, Farmington, CT 06032-1507, USA.

出版信息

Traffic. 2008 Apr;9(4):472-80. doi: 10.1111/j.1600-0854.2007.00698.x. Epub 2007 Dec 26.

Abstract

Cytoplasmic dynein is known to be involved in the establishment of radial microtubule (MT) arrays. During mitosis, dynein activity is required for tethering of the MTs at the spindle poles. In interphase cells, dynein inhibitors induce loss of radial MT organization; however, the exact role of dynein in the maintenance of MT arrays is unclear. Here, we examined the effect of dynein inhibitors on MT distribution and the centrosome protein composition in cultured fibroblasts. We found that while these inhibitors induced rapid (t(1/2) approximately 20 min) loss of radial MT organization, the levels of key centrosomal proteins or the rates of MT nucleation did not change significantly in dynein-inhibited cells, suggesting that the loss of dynein activity does not affect the structural integrity of the centrosome or its capacity to nucleate MTs. Live observations of the centrosomal activity showed that dynein inhibition enhanced the detachment of MTs from the centrosome. We conclude that the primary role of dynein in the maintenance of a radial MT array in interphase cells consists of retention of MTs at the centrosome and hypothesize that dynein has a role in the MT retention, separate from the delivery to the centrosome of MT-anchoring proteins.

摘要

已知细胞质动力蛋白参与径向微管(MT)阵列的形成。在有丝分裂期间,动力蛋白活性对于微管在纺锤体极的锚定是必需的。在间期细胞中,动力蛋白抑制剂会导致径向微管组织的丧失;然而,动力蛋白在维持微管阵列的确切作用尚不清楚。在这里,我们研究了动力蛋白抑制剂对培养的成纤维细胞中微管分布和中心体蛋白组成的影响。我们发现,虽然这些抑制剂诱导径向微管组织迅速(半衰期约20分钟)丧失,但在动力蛋白抑制的细胞中,关键中心体蛋白的水平或微管成核速率没有显著变化,这表明动力蛋白活性的丧失不会影响中心体的结构完整性或其微管成核能力。对中心体活性的实时观察表明,动力蛋白抑制增强了微管从中心体的脱离。我们得出结论,动力蛋白在间期细胞中维持径向微管阵列的主要作用包括将微管保留在中心体,并推测动力蛋白在微管保留中发挥作用,这与将微管锚定蛋白输送到中心体的作用不同。

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