Albertini D F, Herman B, Sherline P
Eur J Cell Biol. 1984 Jan;33(1):134-43.
The involvement of high molecular weight microtubule-associated proteins (HMW-MAPs) in the process of taxol-induced microtubule bundling has been studied using immunofluorescence and electron microscopy. Immunofluorescence microscopy shows that HMW-MAPs are released from microtubules in granulosa cells which have been extracted in a Triton X-100 microtubule-stabilizing buffer (T-MTSB), unless the cells are pretreated with taxol. 1.0 microM taxol treatment for 48 h results in microtubule bundle formation and the retention of HMW-MAPs in these cells upon extraction with T-MTSB. Electron microscopy demonstrates that microtubules in control cytoskeletons are devoid of surface structures whereas the microtubules in taxol-treated cytoskeletons are decorated by globular particles of a mean diameter of 19.5 nm. The assembly of 3 X cycled whole microtubule protein (tubulin plus associated proteins) in vitro in the presence of 1.0 microM taxol, results in the formation of closely packed microtubules decorated with irregularly spaced globular particles, similar in size to those observed in cytoskeletons of taxol-treated granulosa cells. Microtubules assembled in vitro in the absence of taxol display prominent filamentous extensions from the microtubule surface and center-to-center spacings greater than that observed for microtubules assembled in the presence of taxol. Brain microtubule protein was purified into 6 s and HMW-MAP-enriched fractions, and the effects of taxol on the assembly and morphology of these fractions, separately or in combination, were examined. Microtubules assembled from 6 s tubulin alone or 6 s tubulin plus taxol (without HMW-MAPs) were short, free structures whereas those formed in the presence of taxol from 6 s tubulin and a HMW-MAP-enriched fraction were extensively crosslinked into aggregates. These data suggest that taxol induces microtubule bundling by stabilizing the association of HMW-MAPs with the microtubule surface which promotes lateral aggregation.
利用免疫荧光和电子显微镜技术,对高分子量微管相关蛋白(HMW - MAPs)在紫杉醇诱导微管束形成过程中的作用进行了研究。免疫荧光显微镜检查显示,在经Triton X - 100微管稳定缓冲液(T - MTSB)提取的颗粒细胞中,HMW - MAPs会从微管中释放出来,除非细胞先用紫杉醇进行预处理。用1.0 microM紫杉醇处理48小时会导致微管束形成,并且在用T - MTSB提取时,这些细胞中会保留HMW - MAPs。电子显微镜显示,对照细胞骨架中的微管没有表面结构,而紫杉醇处理的细胞骨架中的微管则被平均直径为19.5 nm的球状颗粒所修饰。在1.0 microM紫杉醇存在的情况下,体外组装3次循环的全微管蛋白(微管蛋白加相关蛋白),会形成紧密堆积的微管,这些微管上装饰有间隔不规则的球状颗粒,其大小与在紫杉醇处理的颗粒细胞骨架中观察到的颗粒相似。在没有紫杉醇的情况下体外组装的微管在微管表面和中心到中心的间距方面显示出明显的丝状延伸,大于在有紫杉醇存在的情况下组装的微管所观察到的间距。脑微管蛋白被纯化为6s和富含HMW - MAPs的组分,并分别或联合检查了紫杉醇对这些组分组装和形态的影响。仅由6s微管蛋白或6s微管蛋白加紫杉醇(无HMW - MAPs)组装的微管是短的、游离的结构,而在有紫杉醇存在的情况下由6s微管蛋白和富含HMW - MAPs的组分形成的微管则广泛交联成聚集体。这些数据表明,紫杉醇通过稳定HMW - MAPs与微管表面的结合来诱导微管束形成,从而促进横向聚集。