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使用器官培养技术进行体外精子发生。

In vitro spermatogenesis using an organ culture technique.

作者信息

Yokonishi Tetsuhiro, Sato Takuya, Katagiri Kumiko, Ogawa Takehiko

机构信息

Department of Urology, Yokohama City University Graduate School of Medicine, Kanazawa-ku, Yokohama, Japan.

出版信息

Methods Mol Biol. 2013;927:479-88. doi: 10.1007/978-1-62703-038-0_41.

Abstract

Research on in vitro spermatogenesis has a long history and remained to be an unaccomplished task until very recently. In 2010, we succeeded in producing murine sperm from primitive spermatogonia using an organ culture method. The fertility of the sperm or haploid spermatids was demonstrated by microinsemination. This organ culture technique uses the classical air-liquid interphase method and is based on conditions extensively examined by Steinbergers in 1960s. Among adaptations in the new culture system, application of serum-free media was the most important. The system is very simple and easy to follow.

摘要

体外精子发生的研究历史悠久,直到最近仍是一项未完成的任务。2010年,我们利用器官培养方法成功地从原始精原细胞中产生了小鼠精子。通过显微授精证明了精子或单倍体精子细胞的生育能力。这种器官培养技术采用经典的气液界面方法,基于20世纪60年代斯坦伯格夫妇广泛研究的条件。在新的培养系统的改进中,无血清培养基的应用是最重要的。该系统非常简单且易于操作。

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