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正丁醇在体内和体外均可诱导微管解聚。

n-Butanol induces depolymerization of microtubules in vivo and in vitro.

作者信息

Hirase Ai, Hamada Takahiro, Itoh Tomohiko J, Shimmen Teruo, Sonobe Seiji

机构信息

Graduate School of Life Science, University of Hyogo, Japan.

出版信息

Plant Cell Physiol. 2006 Jul;47(7):1004-9. doi: 10.1093/pcp/pcj055. Epub 2006 May 13.

Abstract

The effects of butanol on microtubules (MTs) were examined by immunofluorescence microscopy. Fragmentation of cortical MTs was induced by n-butanol, but not by s- and t-butanols, in cultured tobacco BY-2 cells. Taxol prevented n-butanol-induced MT fragmentation. Fragmented cortical MTs were still attached to the inner face of the plasma membrane when n-butanol-treated protoplasts were ruptured on the slide glass. Moreover, MTs were depolymerized in the presence of n-butanol in vitro. Therefore, n-butanol is not only an activator of phospholipase D but also an effective MT-depolymerizing agent.

摘要

通过免疫荧光显微镜检查了丁醇对微管(MTs)的影响。在培养的烟草BY-2细胞中,正丁醇可诱导皮层微管断裂,而异丁醇和叔丁醇则不能。紫杉醇可防止正丁醇诱导的微管断裂。当用正丁醇处理的原生质体在载玻片上破裂时,断裂的皮层微管仍附着在质膜的内表面。此外,在体外,微管在正丁醇存在的情况下会解聚。因此,正丁醇不仅是磷脂酶D的激活剂,也是一种有效的微管解聚剂。

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