Frankel F R
Proc Natl Acad Sci U S A. 1976 Aug;73(8):2798-802. doi: 10.1073/pnas.73.8.2798.
The organization and growth of microtubules in cultured mouse macrophages and fibroblasts were examined by indirect immunofluorescence microscopy with antibodies to microtubule protein. In macrophages, microtubules converged at a samll region at the cytocenter. During depolymerization, and repolymerization, this region acted as a microtubule organizing center. Microtubule growth was energy-dependent, but unaffected by dibutyryl-adenosine 3':5'-cyclic monophosphate, cholera toxin, or dibutyryl-guanosine 3':5'-cyclic monophosphate. Fibroblasts, which did not show such a simple microtubule organization as macrophages, contained mainly one or two, but occasionally as many as four, organizing centers during repolymerization. These microtubule organizing centers often appeared as fluorescent rings with a dark center.
用抗微管蛋白抗体通过间接免疫荧光显微镜检查了培养的小鼠巨噬细胞和成纤维细胞中微管的组织和生长情况。在巨噬细胞中,微管在细胞中心的一个小区域汇聚。在解聚和再聚合过程中,该区域充当微管组织中心。微管生长依赖能量,但不受二丁酰腺苷3':5'-环磷酸、霍乱毒素或二丁酰鸟苷3':5'-环磷酸的影响。成纤维细胞不像巨噬细胞那样具有如此简单的微管组织,在再聚合过程中主要含有一两个,但偶尔多达四个组织中心。这些微管组织中心常常呈现为中心黑暗的荧光环。