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Prospects for spermatogenesis in vitro

机译:体外生精的前景

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In recent years, extraordinary progress has been made in a broad range of reproductive technologies, including spermatogonial transplantation in the male. However, effective procedures for the complete recapitulation of spermatogenesis in vitro, including meiosis, have remained elusive. Such procedures have the potential to facilitate (1) mechanistic studies of spermatogenesis, (2) directed genetic modification of the male germ line, and (3) treatment of male factor infertility. Early studies demonstrated the importance of germ cell-Sertoli association for germ cell survival in vitro. Recently, evidence for male germ cell survival and progression through meiosis has been reported for the rat, mouse, and man. We demonstrated the expression of spermatid-specific genes (protamine and transition protein 1) by alginate-encapsulate neonatal bull testis cells after 10 weeks in culture, suggesting that meiosis had occurred. Although identifiable germ cells in these cultures were very sparse, some indication of acrosome development was observed. Following round spermatid injection (ROSI) with presumptive spermatids produced in vitro, 50% of blastocysts produced were diploid and 37% were Y-chromosome positive. Improved culture conditions, which promote germ cell survival, differentiation, and proliferation, are essential for in vitro spermatogenesis (IVS) to become a useful technology. Other approaches to male germ cell manipulation and spermatid production are discussed.
机译:近年来,在广泛的生殖技术方面取得了非凡的进步,包括男性的精原细胞移植。然而,在体外包括精子细胞减生的精子完全重现的有效方法仍然难以捉摸。这样的程序有可能促进(1)精子发生的机理研究,(2)雄性生殖系的定向遗传修饰,以及(3)雄性不育症的治疗。早期研究证明了生殖细胞-睾丸脂联对于体外生殖细胞存活的重要性。最近,已经报道了大鼠,小鼠和人的雄性生殖细胞通过减数分裂存活和发展的证据。我们证明了在培养10周后藻酸盐包裹新生牛睾丸细胞表达的精子特异性基因(鱼精蛋白和过渡蛋白1),表明减数分裂已经发生。尽管这些培养物中可识别的生殖细胞非常稀疏,但仍观察到一些顶体发育的迹象。圆形精子注射(ROSI)与体外产生的推测性精子后,产生的胚泡中有50%是二倍体,而Y染色体阳性是37%。促进生殖细胞存活,分化和增殖的改良培养条件对于体外精子形成(IVS)成为有用的技术至关重要。讨论了男性生殖细胞操纵和精子产生的其他方法。

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