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果蝇中质膜相关位点微管成核的证据。

Evidence for microtubule nucleation at plasma membrane-associated sites in Drosophila.

作者信息

Mogensen M M, Tucker J B

机构信息

Department of Zoology and Marine Biology, University of St Andrews, Fife, UK.

出版信息

J Cell Sci. 1987 Aug;88 ( Pt 1):95-107. doi: 10.1242/jcs.88.1.95.

DOI:10.1242/jcs.88.1.95
PMID:3127404
Abstract

This report is concerned with the nucleation and organization of microtubule bundles that assemble after 'conventional' centrosomal microtubule-organizing centres have been lost. The microtubule bundles in question span the lengths of wing epidermal cells. Bundles extend between hemidesmosomes at the apical cuticle-secreting surfaces of cells and basal attachment desmosomes that unite the dorsal and ventral epidermal layers of developing wing blades. Furthermore, each bundle includes up to 1500 microtubules and most of the microtubules are composed of 15 protofilaments. Individual cells were serially cross-sectioned at an early stage of bundle assembly. The number of microtubule profiles/cell cross-section decreased progressively by up to 59% of the most apical values in section sequences cut from fairly apical to more basal levels in the cells. The apical ends of microtubules were associated with numerous small dense plaque-like sites (diameter 0.1-0.2 micron), which were specialized regions of plasma membranes at the apical surfaces of cells. Many of the microtubules near apical plaques were not well aligned with each other; they 'radiated away' from cell apices. This was in contrast to the situation at more basal levels where most microtubules were oriented parallel to the longitudinal axes of cells. These findings indicate that the relatively dispersed arrays of apical plasma membrane-associated plaques act as microtubule-nucleating sites to initiate basally directed elongation of bundle microtubules. Apical cell surfaces and their plaques seem to operate as microtubule-nucleating and -organizing regions that functionally replace the centrosomal microtubule-organizing centres lost earlier in cell differentiation.

摘要

本报告关注的是在“传统”中心体微管组织中心丧失后组装的微管束的成核与组织。所讨论的微管束跨越翅表皮细胞的长度。这些微管束在细胞顶端角质层分泌表面的半桥粒与连接发育中翅片背腹表皮层的基底附着桥粒之间延伸。此外,每个微管束包含多达1500根微管,且大多数微管由15条原纤维组成。在微管束组装的早期阶段,对单个细胞进行了连续切片。从细胞相当顶端到更基部水平切割的切片序列中,微管轮廓/细胞横截面的数量逐渐减少,最多可降至最顶端值的59%。微管的顶端与众多小的致密斑块状位点(直径0.1 - 0.2微米)相关联,这些位点是细胞顶端表面质膜的特化区域。靠近顶端斑块的许多微管彼此排列不佳;它们从细胞顶端“向外辐射”。这与更基部水平的情况形成对比,在那里大多数微管与细胞的纵轴平行排列。这些发现表明,顶端质膜相关斑块的相对分散排列充当微管成核位点,以启动微管束微管向基部的延伸。顶端细胞表面及其斑块似乎作为微管成核和组织区域,在功能上替代了在细胞分化早期丧失的中心体微管组织中心。

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