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细胞松弛素D对已建系细胞的作用。III. 细胞表面的出芽和运动

Action of cytochalasin D on cells of established lines. III. Zeiosis and movements at the cell surface.

作者信息

Godman G C, Miranda A F, Deitch A D, Tanenbaum S W

出版信息

J Cell Biol. 1975 Mar;64(3):644-67. doi: 10.1083/jcb.64.3.644.

Abstract

The projection of knobby protuberances at the cell surface (zeiosis) is a general cellular response to cytochalasin D (CD), resulting from herniation of endoplasm through undefended places of the cortex during cell contractions and displacement of microfilaments induced by CD. Zeiosis is prevented by agents that interfere with the contractile response to CD, such as inhibitors of energy metabolism or cyclic AMP. The developed protrusions, which remain relatively stable in the presence of CD, contain chiefly mono- or subribosomes, and occasionally other organelles normally resident in endoplasm; compact microfilament felt occupies their bases and extends into their proximal stalks. Protein synthesis in the knobs is less than half of that in the polyribosome-containing endoplasm residual in the main body of the cell. Knobs first protrude singly near the margin of the contracting cells and rapidly cluster into small groups in the periphery even at lower temperature. The clusters then migrate centripetally and coalesce into a large aggregate near the apex of the immobilized and retracted cell: this movement is energy- and temperature-dependent. Aggregation is more prominent and stable in cell lines of epithelial derivation than in fibroblastic or other lines in which nuclear extrusion occurs more readily. The latter is regarded as a special manifestation of zeiosis. Macromarkers, such as latex spherules, migrate like the zeiotic knobs on the cell surfaces in the presence of CD. The aggregated knobs, although persistent for days in the presence of CD, are rapidly recessed after withdrawal of the agent as ruffling is resumed and the cells spread. These movements are discussed in terms of current concepts of mobility of the cell membrane.

摘要

细胞表面出现的瘤状突起(胞质突出)是细胞对细胞松弛素D(CD)的一种普遍反应,这是由于在细胞收缩过程中内质通过皮质未受保护的部位疝出以及CD诱导的微丝移位所致。干扰对CD收缩反应的试剂,如能量代谢抑制剂或环磷酸腺苷,可防止胞质突出。在CD存在下保持相对稳定的已形成的突起主要含有单核糖体或亚核糖体,偶尔还含有内质中通常存在的其他细胞器;致密的微丝毡占据其基部并延伸至其近端柄部。瘤状突起中的蛋白质合成不到细胞主体中含多核糖体的内质中蛋白质合成的一半。瘤状突起首先在收缩细胞边缘附近单个突出,即使在较低温度下也会在周边迅速聚集成小群。然后这些小群向心迁移并在固定和收缩细胞的顶端附近合并成一个大聚集体:这种运动依赖于能量和温度。上皮来源的细胞系中的聚集比成纤维细胞系或其他更容易发生核挤出的细胞系中的聚集更显著和稳定。后者被认为是胞质突出的一种特殊表现。大分子标记物,如乳胶小球,在CD存在下会像细胞表面的胞质突出瘤状突起一样迁移。聚集的瘤状突起虽然在CD存在下能持续数天,但在去除该试剂后,随着细胞恢复皱褶并铺展,会迅速凹陷。这些运动根据当前关于细胞膜流动性的概念进行了讨论。

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