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哺乳动物细胞中微管组装起始的多个位点。

Multiple sites for the initiation of microtubule assembly in mammalian cells.

作者信息

Spiegelman B M, Lopata M A, Kirschner M W

出版信息

Cell. 1979 Feb;16(2):239-52. doi: 10.1016/0092-8674(79)90002-3.

Abstract

The pattern of microtubule regrowth in mammalian fibroblast and epithelial cells has been examined by immunofluorescence of cytoskeletal preparations with antibody to tubulin. After reversal of treatment with colcemid, vinblastine or low temperature, microtubules appear to grow simultaneously from several distinct initiation sites located within 5 microns of the nucleus of mouse and human fibroblasts. Each site initiates the growth of 10-30 microtubules. More than 70% of the mouse fibroblasts have between 5 and 10 initiation sites with an average of 8. The human fibroblasts have an average of 5 sites per cell. The average number and numerical distribution of sites per fibroblast cell are not affected by time of exposure to colcemid or the concentration of colcemid applied to the cells. Multiple microtubule initiation sites are also observed during the process of microtubule depolymerization. In addition to growth from these complex initiation sites, microtubules appear to grow singly from the perinuclear region of human fibroblasts. The regrowth of individual microtubules from the perinuclear growth is especially prominent in epithelial cell lines from rat kangaroo and pig. These epithelial lines have only a single complex initiation site per cell. Two classes of complex initiation sites can be distinguished in microtubule regrowth experiments in human and mouse fibroblasts after exposure to griseofulvin. Microtubules first grow extensively from a single distinct site, which has approximately 20 microtubules growing from it and may be the centriole or centriolar pair. Subsequently, microtubules regrow from other perinuclear complex initiation sites. It thus appears that at least three distinct classes of initiation sites can be observed in mammalian cells: primary sites, which regrow microtubules first after griseofulvin treatment; secondary sites, which are distinct perinuclear sites and recover from griseofulvin treatment more slowly than the primary sites; and tertiary sites or sites of growth of single microtubules, also located near the cell nucleus.

摘要

通过用抗微管蛋白抗体对细胞骨架制剂进行免疫荧光检测,研究了哺乳动物成纤维细胞和上皮细胞中微管重新生长的模式。在用秋水仙酰胺、长春花碱或低温处理后恢复时,微管似乎从位于小鼠和人类成纤维细胞核5微米范围内的几个不同起始位点同时生长。每个位点起始10 - 30根微管的生长。超过70%的小鼠成纤维细胞有5到10个起始位点,平均为8个。人类成纤维细胞平均每个细胞有5个位点。每个成纤维细胞位点的平均数量和数值分布不受秋水仙酰胺暴露时间或施加到细胞上的秋水仙酰胺浓度的影响。在微管解聚过程中也观察到多个微管起始位点。除了从这些复杂起始位点生长外,微管似乎还从人类成纤维细胞的核周区域单个生长。来自大鼠袋鼠和猪的上皮细胞系中,从核周生长的单个微管的重新生长尤为突出。这些上皮细胞系每个细胞只有一个复杂起始位点。在接触灰黄霉素后,在人类和小鼠成纤维细胞的微管重新生长实验中可区分出两类复杂起始位点。微管首先从一个单一的不同位点大量生长,该位点有大约20根微管从其生长,可能是中心粒或中心粒对。随后,微管从其他核周复杂起始位点重新生长。因此,在哺乳动物细胞中似乎可以观察到至少三类不同的起始位点:主要位点,在灰黄霉素处理后首先重新生长微管;次要位点,是不同的核周位点,从灰黄霉素处理中恢复的速度比主要位点慢;第三类位点或单个微管的生长位点,也位于细胞核附近。

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