Sider J R, Mandato C A, Weber K L, Zandy A J, Beach D, Finst R J, Skoble J, Bement W M
Department of Zoology and Program in Cellular and Molecular Biology, University of Wisconsin, Madison, WI, USA.
J Cell Sci. 1999 Jun;112 ( Pt 12):1947-56. doi: 10.1242/jcs.112.12.1947.
Coordinated interplay of the microtubule and actin cytoskeletons has long been known to be crucial for many cellular processes including cell migration and cytokinesis. However, interactions between these two systems have been difficult to document by conventional approaches, for a variety of technical reasons. Here the distribution of f-actin and microtubules were analyzed in the absence of fixation using Xenopus egg extracts as an in vitro source of microtubules and f-actin, demembranated Xenopus sperm to nucleate microtubule asters, fluorescent phalloidin as a probe for f-actin, and fluorescent tubulin as a probe for microtubules. F-actin consistently colocalized in a lengthwise manner with microtubules of asters subjected to extensive washing in flow chambers. F-actin-microtubule association was heterogenous within a given aster, such that f-actin is most abundant toward the distal (plus) ends of microtubules, and microtubules heavily labeled with f-actin are found in close proximity to microtubules devoid of f-actin. However, this distribution changed over time, in that 5 minute asters had more f-actin in their interiors than did 15 minute asters. Microtubule association with f-actin was correlated with microtubule bending and kinking, while elimination of f-actin resulted in straighter microtubules, indicating that the in vitro interaction between f-actin and microtubules is functionally significant. F-actin was also found to associate in a lengthwise fashion with microtubules in asters centrifuged through 30% sucrose, and microtubules alone (i.e. microtubules not seeded from demembranated sperm) centrifuged through sucrose, indicating that the association cannot be explained by flow-induced trapping and alignment of f-actin by aster microtubules. Further, cosedimentation analysis revealed that microtubule-f-actin association could be reconstituted from microtubules assembled from purified brain tubulin and f-actin assembled from purified muscle actin in the presence, but not the absence, of Xenopus oocyte microtubule binding proteins. The results provide direct evidence for an association between microtubules and f-actin in vitro, indicate that this interaction is mediated by one or more microtubule binding proteins, and suggest that this interaction may be responsible for the mutual regulation of the microtubule and actomyosin cytoskeletons observed in vivo.
长期以来,人们一直认为微管和肌动蛋白细胞骨架的协同相互作用对于包括细胞迁移和胞质分裂在内的许多细胞过程至关重要。然而,由于各种技术原因,用传统方法很难记录这两个系统之间的相互作用。在这里,在不进行固定的情况下,使用非洲爪蟾卵提取物作为微管和f-肌动蛋白的体外来源、去膜的非洲爪蟾精子来形成微管星状体、荧光鬼笔环肽作为f-肌动蛋白的探针以及荧光微管蛋白作为微管的探针,分析了f-肌动蛋白和微管的分布。在流动小室中经过大量洗涤的星状体微管中,f-肌动蛋白始终以纵向方式与微管共定位。在给定的星状体内,f-肌动蛋白与微管的结合是异质的,因此f-肌动蛋白在微管的远端(正端)最为丰富,并且在没有f-肌动蛋白的微管附近发现了大量被f-肌动蛋白标记的微管。然而,这种分布随时间变化,因为5分钟的星状体内部的f-肌动蛋白比15分钟的星状体更多。微管与f-肌动蛋白的结合与微管的弯曲和扭结相关,而去除f-肌动蛋白会导致微管更直,这表明f-肌动蛋白与微管在体外的相互作用在功能上具有重要意义。还发现f-肌动蛋白在通过30%蔗糖离心的星状体中以纵向方式与微管结合,并且单独的微管(即不是由去膜精子接种的微管)通过蔗糖离心,这表明这种结合不能用星状体微管对f-肌动蛋白的流动诱导捕获和排列来解释。此外,共沉降分析表明,在存在非洲爪蟾卵母细胞微管结合蛋白的情况下,但在没有这种蛋白的情况下,微管-f-肌动蛋白的结合可以由从纯化的脑微管蛋白组装的微管和从纯化的肌肉肌动蛋白组装的f-肌动蛋白重建。这些结果为微管和f-肌动蛋白在体外的结合提供了直接证据,表明这种相互作用是由一种或多种微管结合蛋白介导的,并表明这种相互作用可能是体内观察到的微管和肌动球蛋白细胞骨架相互调节的原因。