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[培养细胞胞质中微管长度测量的各种方法评估]

[Evaluation of various methods of measurement of the microtubule length in the cytoplasm of cultured cells].

作者信息

Chernobel'skaia O A, Grigor'ev I S, Alieva I B, Vorob'ev I A

机构信息

Belozerskii Research Institute of Physicochemical Biology, Moscow State University, Vorob'evy gory, Moscow, 119899 Russia.

出版信息

Ontogenez. 2001 Jan-Feb;32(1):58-66.

Abstract

It is generally assumed that microtubules in tissue culture cells extend from the centrosome to cell periphery, and the length of individual microtubules averages several dozens of microns. However, direct electron-microscopic measurements have cast some doubt on this assumption. In this study, the average length of microtubules in cultured Vero cells was estimated using a combined approach. The length of free cytoplasmic and centrosomal microtubules was determined by means of electron microscopy in serial sections; concurrently, the length of free microtubules in the lamella was measured in preparations stained with tubulin antibodies (an indirect immunofluorescent method), by tracing saltatory particle movements along the microtubules in living cells. According to the data of immunofluorescent microscopy, microtubule length in the lamella averaged 4.57 +/- 3.69 microns. However, since two or more microtubules can overlap, their length may be slightly overestimated by this method. On the other hand, saltatory movements are easy to monitor and measure fairly accurately, but their range may be shorter than the actual microtubule length because of a limited processiveness of motors (kinesin and dynein). On average, the trajectories of saltatory movements in living cells were 3.85 +/- 0.72 microns long. At the electron-microscopic level, microtubule length was analyzed using pseudo-three-dimensional reconstructions of the microtubule systems around the centrosome and in the lamella. The length of free microtubules in the lamella reached 18 microns, averaging 3.33 +/- 2.43 microns; the average length of centrosomal microtubules was 1.49 +/- 0.82 microns. Good correspondence between the data on microtubule length and arrangement obtained by different methods allows the conclusion that most of free microtubules in Vero cells actually have a length of 2-5 microns; i.e., they are much shorter than the cell radius (about 25 microns). Microtubules extending from the centrosome are shorter still and do not reach the cell periphery. Thus, most microtubules in the lamella of Vero cells are free and their ordered arrangement is not associated with their attachment to the centrosome.

摘要

一般认为,组织培养细胞中的微管从中心体延伸至细胞周边,单个微管的长度平均为几十微米。然而,直接的电子显微镜测量对此假设提出了一些质疑。在本研究中,采用组合方法估计培养的非洲绿猴肾细胞(Vero细胞)中微管的平均长度。通过电子显微镜对连续切片中游离的胞质微管和中心体微管的长度进行测定;同时,在微管蛋白抗体染色的制剂中(间接免疫荧光法),通过追踪活细胞中沿微管跳跃式移动的颗粒,测量片状伪足中游离微管的长度。根据免疫荧光显微镜的数据,片状伪足中的微管长度平均为4.57±3.69微米。然而,由于两根或更多微管可能重叠,通过该方法测量的微管长度可能会被略微高估。另一方面,跳跃式移动易于监测且测量相当准确,但由于驱动蛋白(驱动蛋白和动力蛋白)的持续性有限,其移动范围可能比实际微管长度短。活细胞中跳跃式移动轨迹的平均长度为3.85±0.72微米。在电子显微镜水平上,利用中心体周围和片状伪足中微管系统的伪三维重建分析微管长度。片状伪足中游离微管的长度达18微米,平均为3.33±2.43微米;中心体微管的平均长度为1.49±0.82微米。不同方法获得的微管长度和排列数据之间良好相符,这使得我们可以得出结论:非洲绿猴肾细胞中大多数游离微管的实际长度为2 - 5微米;即,它们比细胞半径(约25微米)短得多。从中心体延伸出的微管更短,无法到达细胞周边。因此,非洲绿猴肾细胞片状伪足中的大多数微管是游离的,其有序排列与它们与中心体的附着无关。

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