Regen C M, Horwitz A F
Department of Cell and Structural Biology, University of Illinois, Urbana 61801.
J Cell Biol. 1992 Dec;119(5):1347-59. doi: 10.1083/jcb.119.5.1347.
Motile chick skeletal fibroblasts adhere to a laminin substrate by means of clustered beta 1 integrins. These integrin "macroaggregates" are similar to classic focal contacts but do not appear dark under interference-reflection microscopy. They contain alpha 5 integrin and are associated with extracellular fibronectin. To study their behavior during cell movement, time-lapse, low-light video microscopy was used to image integrins on living cells tagged with a fluorescent anti-beta 1 integrin antibody. Integrin macroaggregates remain fixed with respect to the substratum, despite the fact that they fluctuate in size, density, and shape over a period of minutes. Upon detachment of the cell rear, as much as 85% of the beta 1 integrin density of a macroaggregate remains behind on the substrate, along with both alpha 5 integrin and fibronectin. Release of the cell rear does not involve cleavage of the beta 1 integrin cytoplasmic domain from the remainder of the protein. These results indicate that cell motility does not require regulated detachment of integrin receptors from the substrate. On the other hand, cytoskeletal components and a variable fraction of the integrins are carried forward with the cell during detachment, suggesting that some type of cortical disassembly process does occur. Integrin macroaggregate structures are not recycled intact after detachment of the cell rear from the substrate. They do not persist on the cell surface, nor can they be seen to be engulfed by vesicles; yet, some of the individual integrins that make up these macroaggregates are eventually transported forward by both vesicular and cell-surface routes. Antibody-tagged integrins accumulate in dense patches at the lateral edges and dorsal surface of the cell, and move forward on the cell surface. The tagged integrins also enter cytoplasmic vesicles, which move forward within the cytoplasm. Macroaggregates generally form and grow at the cell front; however, application of fluorescent antibody causes integrins to disappear from the leading edge. Therefore, it has not been possible to directly visualize the recycling of the forward moving tagged integrins into new macroaggregates at the cell front. Surprisingly, under these conditions cells move normally despite the absence of any delivery of tagged integrin to the leading edge, indicating that recycling of integrins to the lamella is not required for apparently normal motility.
活动的鸡胚骨骼肌成纤维细胞通过聚集的β1整合素黏附于层粘连蛋白底物。这些整合素“大聚集体”类似于经典的黏着斑,但在干涉反射显微镜下看起来并不暗。它们含有α5整合素,并与细胞外纤连蛋白相关。为了研究它们在细胞运动过程中的行为,采用延时、低光视频显微镜对用荧光抗β1整合素抗体标记的活细胞上的整合素进行成像。整合素大聚集体相对于底物保持固定,尽管它们在几分钟内大小、密度和形状会发生波动。在细胞尾部脱离时,一个大聚集体中多达85%的β1整合素密度连同α5整合素和纤连蛋白一起留在底物上。细胞尾部的脱离并不涉及β1整合素胞质结构域与蛋白质其余部分的切割。这些结果表明细胞运动不需要整合素受体从底物上进行调节性脱离。另一方面,细胞骨架成分和可变比例的整合素在脱离过程中随细胞向前移动,这表明确实发生了某种类型的皮质解体过程。在细胞尾部从底物脱离后,整合素大聚集体结构不会完整回收。它们不会持续存在于细胞表面,也看不到被小泡吞噬;然而,构成这些大聚集体的一些单个整合素最终会通过小泡和细胞表面途径向前运输。抗体标记的整合素在细胞的侧边缘和背表面的致密斑块中积累,并在细胞表面向前移动。标记的整合素也进入细胞质小泡,这些小泡在细胞质内向前移动。大聚集体通常在细胞前端形成并生长;然而,应用荧光抗体导致整合素从前缘消失。因此,无法直接观察到向前移动的标记整合素在细胞前端重新进入新的大聚集体的循环过程。令人惊讶的是,在这些条件下,尽管没有任何标记整合素输送到前缘,细胞仍能正常移动,这表明整合素循环到片层对于明显正常的运动不是必需的。