Keller H, Eggli P
Department of Pathology, University of Bern, Switzerland.
Cell Motil Cytoskeleton. 1998;41(2):181-93. doi: 10.1002/(SICI)1097-0169(1998)41:2<181::AID-CM8>3.0.CO;2-H.
The dynamic events at the front of locomoting blebbing Walker carcinosarcoma cells [Keller and Bebie, Cell Motil. Cytoskeleton 33:241-251, 1996] are interpreted on the basis of an analysis of the actin cytoskeleton and its relationship to the plasma membrane in fixed cells using a novel double-staining procedure. The data show that blebs are formed where cortical actin is locally depolymerized and/or by detachment of the plasma membrane from more or less intact cortical actin layers. Dissociation between the cortical actin layer and the plasma membrane, which is stimulated by microtubule disassembly, is achieved by forward movement of the plasma membrane, rather than by retraction of the actin layer. Therefore, the detached actin layers form a boundary between the newly forming protrusions and the rest of the cell. They can be associated with "constriction rings," which we have termed "restriction rings." Detached actin layers can impede entry of organelles and the nucleus into the protrusions and thereby compartmentalize the cytoplasm. Later, detached cortical actin layers depolymerize, allowing for relaxation of the restriction rings and for forward movement of cytoplasmic organelles and the nucleus. Actin may repolymerize along the detached plasma membrane allowing for a new cycle to occur. Estimates indicate that the actin polymerization/depolymerization cycles may be largely confined to the front of blebbing cells. The findings suggest that the dynamic events at the front of blebbing metazoan cells are similar to those previously found in Amoeba proteus [Grebecki, Protoplasma, 154:98-111, 1990] but different from those found in lamellipodia.
运用一种全新的双重染色方法,通过对固定细胞中肌动蛋白细胞骨架及其与质膜的关系进行分析,阐释了游动泡状沃克癌肉瘤细胞前沿的动态事件[凯勒和贝比,《细胞运动与细胞骨架》33:241 - 251,1996]。数据表明,泡状结构在皮质肌动蛋白局部解聚的部位形成,和/或通过质膜与或多或少完整的皮质肌动蛋白层分离而形成。皮质肌动蛋白层与质膜之间的解离,由微管解聚所刺激,是通过质膜的向前移动实现的,而非肌动蛋白层的回缩。因此,分离的肌动蛋白层在新形成的突起与细胞其余部分之间形成边界。它们可能与“收缩环”相关,我们将其称为“限制环”。分离的肌动蛋白层会阻碍细胞器和细胞核进入突起,从而使细胞质分隔开来。随后,分离的皮质肌动蛋白层解聚,使得限制环松弛,细胞质细胞器和细胞核能够向前移动。肌动蛋白可能会沿着分离的质膜重新聚合,从而开启新的循环。估计表明,肌动蛋白的聚合/解聚循环可能主要局限于泡状细胞的前沿。这些发现表明,后生动物泡状细胞前沿的动态事件与先前在变形虫中发现的类似[格雷贝茨基,《原生质体》,154:98 - 111,1990],但与片足中发现的不同。