Ogawa T, Aréchaga J M, Avarbock M R, Brinster R L
Laboratory of Reproductive Physiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia 19104-6009, USA.
Int J Dev Biol. 1997 Feb;41(1):111-22.
In the adult male, germ cell differentiation takes place in the seminiferous tubules of the testis by a complex, highly organized and very efficient process. A population of diploid stem-cell spermatogonia that lie on the basement membrane of the tubule continuously undergoes self-renewal and produces progeny cells, which initiate the process of cellular differentiation to generate mature spermatozoa. Each testis contains many seminiferous tubules, which are connected at both ends to a collecting system called the rete testis. The mature spermatozoa pass from the tubules into the rete and are then carried through efferent ducts to the epididymis for final maturation before they are ready to fertilize an egg. In previous studies, we have demonstrated that donor testis cells collected from a fertile mouse are able to generate spermatogenesis when transplanted to the seminiferous tubules of an infertile male. The spermatozoa produced by the recipient from the donor-derived spermatogonial stem cells are able to fertilize eggs and produce progeny carrying the donor male haplotype. Furthermore, donor testis stem cells from a rat will generate normal rat spermatozoa following transplantation to a mouse testis. The spermatogonial transplantation technique is clearly valuable and applicable to many species, but it is difficult. Therefore, several procedures to introduce donor cells into the seminiferous tubules of a recipient have been developed using the mouse as a model, and they are described here in detail. The results indicate that microinjection of cell suspensions into the seminiferous tubules, efferent ducts or rete testis are equally effective in generating donor cell-derived spermatogenesis in recipients. Each approach is likely to be useful for different experimental purposes in a variety of species.
在成年雄性中,生殖细胞分化通过一个复杂、高度有序且非常高效的过程在睾丸的生精小管中发生。位于小管基底膜上的一群二倍体干细胞精原细胞持续进行自我更新并产生子代细胞,这些子代细胞启动细胞分化过程以生成成熟精子。每个睾丸包含许多生精小管,其两端与一个称为睾丸网的集合系统相连。成熟精子从生精小管进入睾丸网,然后通过输出小管被输送到附睾进行最终成熟,之后才准备好使卵子受精。在先前的研究中,我们已经证明,从可育小鼠收集的供体睾丸细胞移植到不育雄性的生精小管中时能够产生精子发生。受体由供体来源的精原干细胞产生的精子能够使卵子受精并产生携带供体雄性单倍型的后代。此外,大鼠的供体睾丸干细胞移植到小鼠睾丸后将产生正常的大鼠精子。精原细胞移植技术显然具有价值且适用于许多物种,但操作困难。因此,已经开发了几种以小鼠为模型将供体细胞引入受体生精小管的方法,在此详细描述。结果表明,将细胞悬液显微注射到生精小管、输出小管或睾丸网中在受体中产生供体细胞来源的精子发生方面同样有效。每种方法可能对各种物种的不同实验目的有用。