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脊椎动物组织培养细胞中异常的分裂沟:对胞质分裂机制的见解

Unusual cleavage furrows in vertebrate tissue culture cells: insights into the mechanisms of cytokinesis.

作者信息

Sanger J M, Dome J S, Sanger J W

机构信息

Department of Cell and Developmental Biology, University of Pennsylvania, School of Medicine, Philadelphia 19104-6058, USA.

出版信息

Cell Motil Cytoskeleton. 1998;39(2):95-106. doi: 10.1002/(SICI)1097-0169(1998)39:2<95::AID-CM1>3.0.CO;2-F.

Abstract

In cultures of the epithelial cell lines, PtK2 and LLC-PK, some cells assume unusually large flattened morphologies and, during cell division, produce unusual cleavage furrows. We have microinjected some of these large cells with fluorescent actin and myosin probes to determine how the cell's shape and the position of its mitotic spindle affect the deposition of actin and myosin in the forming cleavage furrow. In cells with two spindles, contractile proteins were recruited not only to the cortex bordering the former metaphase plates but also to the cortex midway between each pair of adjacent nondaughter poles or centrosomes. The furrowing between adjacent poles seen in these cultured epithelial cells conformed to the furrows seen when echinoderm eggs were manipulated into a torus shape so that the poles of two mitotic spindles were adjacent to one another [Rappaport, 1961]. The recruitment of contractile proteins and the formation of furrows between adjacent centrosomes was a function of the distances between them. When adjacent centrosomes were positioned too close together neither contractile protein recruitment nor furrow formation occurred. If a normal-sized spindle was present in a very large cell, fibers of contractile protein assembled in the cortex above the former metaphase plate but they did not extend to the cell periphery, resulting in an inhibition of cytokinesis. In all injected cells, the recruitment of actin and myosin to the cell surfaces could first be detected at mid-anaphase before there was any visible sign of furrowing. Our results suggest that vertebrate cells share common mechanisms for the establishment of the cleavage furrow with echinoderm cells. The results are consistent with a model in which (1) the positions of the centrosomes and their linearly connected microtubules determine the position for the assembly of the cleavage furrow, and (2) the signal arrives at the surface within a few minutes after the initiation of anaphase. We speculate that an interaction of the ends of microtubules from adjacent centrosomes with the cell surface promotes a clustering of integral membrane protein(s) that interact with and target contractile proteins to a position midway between centrosomes where furrowing occurs.

摘要

在上皮细胞系PtK2和LLC - PK的培养物中,一些细胞呈现出异常大的扁平形态,并且在细胞分裂期间产生异常的分裂沟。我们已用荧光肌动蛋白和肌球蛋白探针显微注射了其中一些大细胞,以确定细胞的形状及其有丝分裂纺锤体的位置如何影响肌动蛋白和肌球蛋白在形成的分裂沟中的沉积。在具有两个纺锤体的细胞中,收缩蛋白不仅被募集到与先前中期板相邻的皮质,而且还被募集到每对相邻的非子代极或中心体之间的中间皮质。在这些培养的上皮细胞中观察到的相邻极之间的沟与将棘皮动物卵操纵成环形使得两个有丝分裂纺锤体的极彼此相邻时所看到的沟一致[拉帕波特,1961]。收缩蛋白的募集以及相邻中心体之间沟的形成是它们之间距离的函数。当相邻中心体放置得太靠近时,既不会发生收缩蛋白的募集也不会形成沟。如果在非常大的细胞中存在正常大小的纺锤体,收缩蛋白纤维会在前中期板上方的皮质中组装,但它们不会延伸到细胞周边,从而导致胞质分裂受到抑制。在所有注射的细胞中,在有任何可见的沟形成迹象之前,在后期中期就可以首先检测到肌动蛋白和肌球蛋白向细胞表面的募集。我们的结果表明,脊椎动物细胞与棘皮动物细胞在建立分裂沟方面具有共同机制。这些结果与一个模型一致,在该模型中:(1)中心体及其线性连接的微管的位置决定了分裂沟组装的位置;(2)信号在后期开始后几分钟内到达表面。我们推测,来自相邻中心体的微管末端与细胞表面的相互作用促进了整合膜蛋白的聚集,这些整合膜蛋白与收缩蛋白相互作用并将其靶向到发生沟形成的中心体之间的中间位置。

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