Stearns M E, Wang M
Department of Pharmacology, Fox Chase Cancer Center, Philadelphia, PA 19111.
J Cell Sci. 1987 May;87 ( Pt 4):565-80. doi: 10.1242/jcs.87.4.565.
We have re-examined the involvement of microtubules in the process of pigment granule transport in squirrelfish erythrophores in situ (i.e. on scales). Light-microscopic studies revealed that following exposure to 5 microM-nocodazole for 1 h at 4 degrees C erythrophores retained an ability to aggregate and disperse their pigment uniformly, though at reduced rates. Serial thick-section stereo high-voltage electron-microscopic studies showed that the entire microtubule population was removed by drug treatment and that the microtubules were not reassembled as a result of pigment translocation processes in the presence of reduced levels of nocodazole (0.4 microM). Immunofluorescence microscopic studies confirmed that nocodazole (0.5-1 microM) produced rapid disassembly of the microtubules. Whole-mount electron-microscopic studies showed that the pigment granules were suspended in a cross-linking network of 3-10 nm filaments, which appeared to support ordered pigment transport in situ in the absence of microtubules. Drug inhibition studies showed that micromolar levels of estramustine, a novel anti-MAPs (microtubule-associated proteins) drug, reversibly inhibited pigment transport. The results suggest that an estramustine-sensitive cytomatrix component might produce polarized pigment transport in intact erythrophores.
我们重新研究了微管在松鼠鱼红色素细胞原位(即在鳞片上)色素颗粒运输过程中的作用。光学显微镜研究显示,在4℃下用5微摩尔诺考达唑处理1小时后,红色素细胞仍有能力均匀地聚集和分散其色素,尽管速率有所降低。连续厚切片立体高压电子显微镜研究表明,药物处理使整个微管群体消失,并且在诺考达唑水平降低(0.4微摩尔)的情况下,微管不会因色素转运过程而重新组装。免疫荧光显微镜研究证实,诺考达唑(0.5 - 1微摩尔)能使微管迅速解体。整装电子显微镜研究表明,色素颗粒悬浮在3 - 10纳米细丝的交联网络中;在没有微管的情况下,该网络似乎支持原位有序的色素运输。药物抑制研究表明,微摩尔水平的雌莫司汀(一种新型抗微管相关蛋白药物)可可逆地抑制色素运输。结果表明,一种对雌莫司汀敏感的细胞基质成分可能在完整的红色素细胞中产生极化色素运输。