Salles-Passador I, Moisand A, Planques V, Wright M
Laboratoire de Pharmacologie, C.N.R.S., Toulouse, France.
J Cell Sci. 1991 Nov;100 ( Pt 3):509-20. doi: 10.1242/jcs.100.3.509.
It has been claimed that the plasmodium of the myxomycete Physarum polycephalum constitutes a very unusual syncytium, devoid of cytoplasmic microtubules. In contrast, we have observed a cytoplasmic microtubule network, by both electron microscopy and immunofluorescence in standard synchronous plasmodia, either in semi-thin sections or in smears, and in thin plasmodia, used as a convenient model. Cytoplasmic microtubules could be seen after immunofluorescent staining with three different monospecific monoclonal anti-tubulin antibodies. The immunolabelling was strictly restricted to typical microtubules as shown by electron microscopy. These cytoplasmic microtubules were entirely and reversibly disassembled by cold treatment and by either of two microtubule poisons: methyl benzimidazole carbamate and griseofulvin. The microtubule network, present in all strains that have been studied, contains single microtubules and microtubule bundles composed of two to eight microtubules. Cytoplasmic microtubules form a dense and complex three-dimensional network, distinct from the microfilamentous domains and from the nuclei. The orientation of the microtubule network varies according to the plasmodial domain examined. Generally microtubules show no special orientation except in plasmodial veins where they are oriented parallel to the long axis of the veins. Differences between our observations and those of previous workers who failed to find cytoplasmic microtubules in plasmodia are discussed. We propose that they reflect difficulties of observation mainly due to the fluorescent background. In contrast with the previous view, the discovery of a microtubule cytoplasmic cytoskeleton in Physarum plasmodia raises several questions concerning its relationships with other cellular organelles and its dynamics during different cell cycle events.
有人声称,多头绒泡菌的疟原虫构成了一种非常特殊的合体细胞,没有细胞质微管。相比之下,我们通过电子显微镜和免疫荧光技术,在标准同步原质团的半薄切片或涂片以及用作便捷模型的薄原质团中,观察到了细胞质微管网络。用三种不同的单特异性抗微管蛋白单克隆抗体进行免疫荧光染色后,可以看到细胞质微管。如电子显微镜所示,免疫标记严格局限于典型的微管。这些细胞质微管通过冷处理以及两种微管毒物之一:甲基苯并咪唑氨基甲酸酯和灰黄霉素,完全且可逆地解聚。在所研究的所有菌株中都存在的微管网络,包含单微管和由两到八根微管组成的微管束。细胞质微管形成一个密集且复杂的三维网络,与微丝区域和细胞核不同。微管网络的方向根据所检查的原质团区域而变化。一般来说,微管没有特殊的方向,除了在原质团脉管中,它们与脉管的长轴平行排列。讨论了我们的观察结果与之前未能在原质团中发现细胞质微管的研究人员的观察结果之间的差异。我们认为,这些差异主要反映了观察上的困难,这主要是由于荧光背景造成的。与之前的观点相反,在多头绒泡菌原质团中发现微管细胞质细胞骨架引发了几个关于它与其他细胞器的关系以及在不同细胞周期事件中的动态变化的问题。