Yoshida T, Ioshii S O, Imanaka-Yoshida K, Izutsu K
Department of Pathology, Mie University School of Medicine, Japan.
J Cell Sci. 1994 Mar;107 ( Pt 3):625-33. doi: 10.1242/jcs.107.3.625.
During spermiogenesis, the shape of the spermatid nucleus, which is spherical, changes and it becomes the sperm head. A microtubular structure called a manchette is thought to be involved in this morphogenetic process. In this report, we demonstrate the localization of cytoplasmic dynein and manchette development by a double immunofluorescence technique using anti-bovine brain MAP 1C and anti-tubulin. Before step 6 of the Leblond and Clermont staging, the microtubules showed a fine reticular network, and the dynein staining was homogeneous. In step 6, the microtubular network was concentrated around the nucleus. The manchette developed in step 7 spermatids, and was fully formed, with a skirt-like appearance, covering the nuclear surface in step 8. Dynein fluorescence was associated with the microtubular manchette in steps 7-10. During these steps, the nucleus was protruded from the cytoplasm. In steps 11-13, the most active stages in nuclear shaping, the dynein was densely localized at the nuclear surface covered by the manchette. As the nucleus acquired a shape similar to the mature spermatozoon at step 14, the dynein fluorescence was localized only at the concave side of the nuclear caudal edge. The manchette became narrower and elongated. In step 15, the manchette extended into the elongated cytoplasm, diminishing during steps 16-18. The localization of the dynein was limited to the ventral aspect of the caudal head in these steps. There was little dynein fluorescence in mature spermatozoa. Immunoelectron microscopy showed positive reactions in the nuclear envelope and the inner region of the microtubular manchette. These observations suggest that cytoplasmic dynein, possibly bound to the nuclear envelope, and manchette microtubules are involved in the protrusion of the spermatid nucleus from the cytoplasm.
在精子发生过程中,呈球形的精子细胞核形状发生变化,形成精子头部。一种称为袖套的微管结构被认为参与了这一形态发生过程。在本报告中,我们通过使用抗牛脑微管相关蛋白1C和抗微管蛋白的双重免疫荧光技术,展示了细胞质动力蛋白的定位和袖套的发育过程。在勒布朗德和克莱蒙分期的第6步之前,微管呈现出精细的网状结构,动力蛋白染色均匀。在第6步时,微管网络集中在细胞核周围。袖套在第7步的精子细胞中开始发育,并在第8步时完全形成,呈裙状外观,覆盖在核表面。在第7 - 10步中,动力蛋白荧光与微管袖套相关。在这些步骤中,细胞核从细胞质中突出。在第11 - 13步,即细胞核塑形最活跃的阶段,动力蛋白密集地定位在被袖套覆盖的核表面。当细胞核在第14步获得类似于成熟精子的形状时,动力蛋白荧光仅定位在核尾缘的凹面。袖套变得更窄并拉长。在第15步,袖套延伸到拉长的细胞质中,并在第16 - 18步逐渐减少。在这些步骤中,动力蛋白的定位仅限于尾头的腹侧。成熟精子中几乎没有动力蛋白荧光。免疫电子显微镜显示在核膜和微管袖套的内部区域有阳性反应。这些观察结果表明,可能与核膜结合的细胞质动力蛋白和袖套微管参与了精子细胞核从细胞质中的突出过程。