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细胞质片段的自主运动。

Autonomous movements of cytoplasmic fragments.

作者信息

Albrecht-Buehler G

出版信息

Proc Natl Acad Sci U S A. 1980 Nov;77(11):6639-43. doi: 10.1073/pnas.77.11.6639.

DOI:10.1073/pnas.77.11.6639
PMID:6935675
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC350342/
Abstract

Tiny fragments from the cytoplasm of human skin fibroblasts with about 2% of the original cell volume ("microplasts") were prepared by treatment with cytochalasin B, vigorous pipetting, and trypsinization of the attached fragments. They remained alive for 8 hr or longer. Some of the microplasts were able to produce and move filopodia, ruffle, or both; others blebbed continuously. Slow flattening was observed in the larger microplasts. In all cases tested, microplasts avoided contact with other cells or microplasts. The observations suggest that the cytoplasmic matrix and the membranes of animal cells are so constructed as to express locally and autonomously any one of the elementary amoeboid movements listed above. More importantly, whatever types of motile surface projections a microplast expressed, it continued to produce and move them in a stereotypical way as if there were long-lived structural or material determinants for each type. The microplasts were unable to locomote autonomously. Therefore, it is conceivable that directional movement of whole cells may require a supervising mechanism that confers a certain coordination and strategy on its component cytoplasmic bits. Otherwise they would continue to move in stereotypical and autonomous ways without ever displacing themselves, as suggested by the behavior of the microplasts.

摘要

通过用细胞松弛素B处理、剧烈吹打以及对附着碎片进行胰蛋白酶消化,制备出了来自人皮肤成纤维细胞胞质的微小碎片,其体积约为原始细胞的2%(“微质体”)。它们能存活8小时或更长时间。一些微质体能够产生并移动丝状伪足、褶皱,或两者皆有;其他的则持续出现泡状突出。在较大的微质体中观察到缓慢变平的现象。在所有测试的情况下,微质体都避免与其他细胞或微质体接触。这些观察结果表明,动物细胞的细胞质基质和膜的构建方式使得它们能够局部自主地表现出上述任何一种基本的阿米巴样运动。更重要的是,无论微质体表现出何种类型的能动表面突起,它都会以一种刻板的方式持续产生并移动这些突起,就好像每种类型都有长寿的结构或物质决定因素一样。微质体无法自主移动。因此,可以想象,整个细胞的定向运动可能需要一种监督机制,该机制赋予其组成的细胞质部分一定的协调性和策略。否则,正如微质体的行为所表明的那样,它们将继续以刻板和自主的方式移动,而永远不会移动自身。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3472/350342/d0a75bc61757/pnas00498-0395-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3472/350342/46ab8fc0c7b7/pnas00498-0393-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3472/350342/bf304606fcb1/pnas00498-0393-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3472/350342/7abf4ea70cc2/pnas00498-0394-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3472/350342/d0a75bc61757/pnas00498-0395-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3472/350342/46ab8fc0c7b7/pnas00498-0393-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3472/350342/bf304606fcb1/pnas00498-0393-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3472/350342/7abf4ea70cc2/pnas00498-0394-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3472/350342/d0a75bc61757/pnas00498-0395-a.jpg

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