首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Hormonal induction of all stages of spermatogenesis in vitro in the male Japanese eel (Anguilla japonica).
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Hormonal induction of all stages of spermatogenesis in vitro in the male Japanese eel (Anguilla japonica).

机译:雄性日本鳗鱼(Anguilla japonica)在体外对精子发生各个阶段的激素诱导。

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摘要

The importance of gonadotropins and androgens for spermatogenesis is generally accepted in vertebrates, but the role played by specific hormones has not been clarified. Under cultivation conditions, male Japanese eels (Anguilla japonica) have immature testes containing only premitotic spermatogonia, type A and early-type B spermatogonia. In the present study, a recently developed organ-culture system for eel testes was used to determine in vitro effects of various steroid hormones on spermatogenesis. After 9 days of culture in serum-free, chemically defined medium containing 11-ketotestosterone (10 ng/ml), a major androgen in male eels, type A and early-type B spermatogonia began mitosis, producing late-type B spermatogonia. After 18 days, zygotene spermatocytes with synaptonemal complexes appeared, indicating that meiosis had already started by this time. In testis fragments cultured for 21 days, round spermatids and spermatozoa were observed with spermatogenic cells at all stages of development. Addition of 11-ketotestosterone to the culture medium also caused a marked cytological activation of Sertoli cells. No other steroid hormones tested had such stimulatory effects. These results, together with our earlier observations, suggest the following sequence for the hormonal induction of spermatogenesis in eel testes; gonadotropin stimulates the Leydig cells to produce 11-ketotestosterone, which, in turn, activates the Sertoli cells leading to the completion of spermatogenesis. This is, thus, an example of an animal system in which all stages of spermatogenesis have been induced by hormonal manipulation in vitro.
机译:促性腺激素和雄激素对精子发生的重要性在脊椎动物中已被普遍接受,但具体激素所起的作用尚未阐明。在栽培条件下,雄性日本鳗els(Anguilla japonica)的睾丸未成熟,仅含有有丝分裂的精原细胞,A型和B型早期精原细胞。在本研究中,最近开发的鳗test睾丸器官培养系统用于确定各种类固醇激素对精子发生的体外作用。在含有11-酮睾丸酮(10 ng / ml)的无血清化学成分确定的培养基中培养9天后,雄性鳗鱼(A型和B型早期精原细胞)中的主要雄激素开始有丝分裂,产生B型晚期精原细胞。 18天后,出现带有突触复合物的合子精子细胞,表明此时已经开始减数分裂。在培养21天的睾丸碎片中,在发育的各个阶段均观察到圆形的精子和精子与生精细胞。向培养基中添加11-酮睾酮也引起Sertoli细胞的明显细胞学活化。没有其他测试的类固醇激素具有这种刺激作用。这些结果,加上我们较早的观察结果,提示了激素诱导鳗鱼睾丸生精的以下顺序。促性腺激素刺激Leydig细胞产生11-酮睾酮,进而激活Sertoli细胞,导致精子发生完成。因此,这是动物系统的一个例子,其中精子发生的所有阶段都已通过荷尔蒙的体外操纵而被诱导。

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