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长春碱诱导的SV40转化的3T3小鼠成纤维细胞中微管支架的超微结构转变。

Vinblastine-induced ultrastructural transition of microtubular scaffoldings in the SV40-transformed 3T3 murine fibroblasts.

作者信息

Fan Dominic, Voelz Herbert G

机构信息

Department of Cancer Biology, The University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

J Exp Ther Oncol. 2009;8(2):85-94.

Abstract

SV40-transformed 3T3 cells (SV3T3) treated with the antitubulin chemotherapeutic agent vinblastine exhibited ultrastructural alterations in their cellular microtubular scaffolding by electron microscopy. Apparent disappearance of the subcellular microtubules occurred after the cells were incubated with vinblastine at 10 microg/ml at 37 degrees C for 8 hours. Typical cytoplasmic microtubular crystals were found with additional smooth membrane-limited vesicles. These vesicles mimic the differentiation cellular organelle called annulated lamellae. Microtubules were frequently seen associated with the Golgi apparatus and rough endoplasmic reticulum in the SV3T3 cells. These microtubules may contribute to transport of products between the Golgi and the rough endoplasmic reticulum. When treated with vinblastine, microtubular crystals were also observed between the Golgi and the rough endoplasmic reticulum. The size and numbers of cytoplasmic inclusions were increased in vinblastine-treated cells. In the SV3T3 cells, microtubules are determined by image analysis to be 230 A degrees in diameter with a subunit wall of 45 A degrees thick. These microtubules have a center-to-center space of 55.6 A degrees between the protofilaments. The skewed heterodimeric microtubular subunits are composed of disk-like structures of 45 A degrees in length, 30 A degrees in width, and 20 A degrees in thickness. The subunit center-to-center skewed angle is 40 degree. After the cells were treated with vinblastine, the microtubules undergo a transitional dissociation, and reassemble into ordered crystals. These transitional microtubules have an increased diameter of 350 A degrees, and a larger protofilament center-to-center space of 85 A degrees. These morphometric measurements indicated that there is a critical microtubule dissociation distance of 30 A degrees, exceeded which the typical microtubular ultrastructure may no longer exist.

摘要

用抗微管蛋白化疗药物长春花碱处理的猿猴病毒40(SV40)转化的3T3细胞(SV3T3),通过电子显微镜观察发现其细胞微管支架出现超微结构改变。在37℃下将细胞与10微克/毫升长春花碱孵育8小时后,亚细胞微管明显消失。发现典型的细胞质微管晶体以及额外的光滑膜包被小泡。这些小泡类似于称为环层板的分化细胞器。在SV3T3细胞中经常可见微管与高尔基体和粗面内质网相关联。这些微管可能有助于高尔基体和粗面内质网之间产物的运输。用长春花碱处理后,在高尔基体和粗面内质网之间也观察到微管晶体。长春花碱处理的细胞中细胞质内含物的大小和数量增加。在SV3T3细胞中,通过图像分析确定微管直径为230埃,亚基壁厚45埃。这些微管原纤维之间的中心间距为55.6埃。倾斜的异二聚体微管亚基由长度为45埃、宽度为30埃、厚度为20埃的盘状结构组成。亚基中心间倾斜角度为40度。细胞用长春花碱处理后,微管经历过渡性解离,并重新组装成有序晶体。这些过渡性微管直径增加到350埃,原纤维中心间距更大,为85埃。这些形态测量表明存在30埃的关键微管解离距离,超过此距离,典型的微管超微结构可能不再存在。

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