Moreno Ricardo D, Palomino Jaime, Schatten Gerald
Unit of Reproduction and Developmental Biology, Physiology Department, Faculty of Biological Sciences, Pontifical Catholic University of Chile, Portugal 49-Santiago 340-213, Chile.
Dev Biol. 2006 May 1;293(1):218-27. doi: 10.1016/j.ydbio.2006.02.001. Epub 2006 Mar 15.
The acrosome is a secretory vesicle attached to the nucleus of the sperm. Our hypothesis is that microtubules participate in the membrane traffic between the Golgi apparatus and acrosome during the first steps of spermatid differentiation. In this work, we show that nocodazole-induced microtubule depolarization triggers the formation of vesicles of the acrosomal membrane, without detaching the acrosome from the nuclear envelope. Nocodazole also induced fragmentation of the Golgi apparatus as determined by antibodies against giantin, golgin-97 and GM130, and electron microscopy. Conversely, neither the acrosome nor the Golgi apparatus underwent fragmentation in elongating spermatids (acrosome- and maturation-phase). The microtubule network of round spermatids of azh/azh mice also became disorganized. Disorganization correlated with fragmentation of the acrosome and the Golgi apparatus, as evaluated by domain-specific markers. Elongating spermatids (acrosome and maturation-phase) of azh/azh mice also had alterations in microtubule organization, acrosome, and Golgi apparatus. Finally, the spermatozoa of azh/azh mice displayed aberrant localization of the acrosomal protein sp56 in both the post-acrosomal and flagellum domains. Our results suggest that microtubules participate in the formation and/or maintenance of the structure of the acrosome and the Golgi apparatus and that the organization of the microtubules in round spermatids is key to sorting acrosomal proteins to the proper organelle.
顶体是附着于精子细胞核的分泌小泡。我们的假设是,在精子细胞分化的最初阶段,微管参与高尔基体与顶体之间的膜运输。在这项研究中,我们发现诺考达唑诱导的微管去极化会触发顶体膜小泡的形成,而不会使顶体与核膜分离。诺考达唑还会诱导高尔基体碎片化,这通过抗巨蛋白、高尔基体蛋白97和GM130的抗体以及电子显微镜得以确定。相反,在伸长精子细胞(顶体和成熟阶段)中,顶体和高尔基体均未发生碎片化。azh/azh小鼠圆形精子细胞的微管网络也变得紊乱。通过结构域特异性标记评估,这种紊乱与顶体和高尔基体的碎片化相关。azh/azh小鼠的伸长精子细胞(顶体和成熟阶段)在微管组织、顶体和高尔基体方面也存在改变。最后,azh/azh小鼠的精子在顶体后和鞭毛区域均显示顶体蛋白sp56的异常定位。我们的结果表明,微管参与顶体和高尔基体结构的形成和/或维持,并且圆形精子细胞中微管的组织对于将顶体蛋白分选到合适的细胞器至关重要。