体内基因转移到睾丸和精子:发展和未来的应用。

Kevin Coward, Hiroki Kubota, John Parrington
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引用次数: 31

摘要

尽管通过辅助生殖技术(ART)治疗不育症取得了重大进展,但特发性男性不育症的根本原因仍不清楚。越来越多的证据表明,与睾丸基因表达相关的疾病可能在男性不育中起重要作用。为了能够充分研究精子发生和受精的分子机制,有必要对男性生殖细胞中的基因表达进行调控。由于目前还没有可靠的方法来重现精子发生培养,因此开发替代性的转基因方法对于研究睾丸和精子的基因功能至关重要。建立转基因动物的方法在很大程度上依赖于将DNA注射到原核中或将转染的胚胎干细胞注射到囊胚中形成嵌合体。尽管这两种方法在制造转基因和基因敲除动物方面取得了成功,但对转基因整合的成本和效率的担忧仍然存在。因此,正在努力评估可选的方法。目前,人们对利用精子作为基因转移载体的方法非常感兴趣。这些方法,包括睾丸介导的基因转移(TMGT)和精子介导的基因转移(SMGT),在不育研究和创造转基因动物方面具有很大的潜力。本文的目的是简要介绍这一领域的发展,并讨论如何将这些基因转移方法有效地应用于未来的研究和临床领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vivo gene transfer into testis and sperm: developments and future application.

Despite significant advances in the treatment of infertility via assisted reproductive technology (ART), the underlying causes of idiopathic male infertility still remain unclear. Accumulating evidence suggests that disorders associated with testicular gene expression may play an important role in male infertility. To be able to fully study the molecular mechanisms underlying spermatogenesis and fertilization, it is necessary to manipulate gene expression in male germ cells. Since there is still no reliable method of recapitulating spermatogenesis culture, the development of alternative transgenic approaches is paramount in the study of gene function in testis and sperm. Established methods of creating transgenic animals rely heavily upon injection of DNA into the pronucleus or the injection of transfected embryonic stem cells into blastocysts to form chimeras. Despite the success of these two approaches for making transgenic and knockout animals, concerns remain over costs and the efficiency of transgene integration. Consequently, efforts are in hand to evaluate alternative methodologies. At present, there is much interest in developing approaches that utilize spermatozoa as vectors for gene transfer. These approaches, including testis mediated gene transfer (TMGT) and sperm mediated gene transfer (SMGT), have great potential as tools for infertility research and in the creation of transgenic animals. The aim of this short review is to briefly describe developments in this field and discuss how these gene transfer methods might be used effectively in future research and clinical arenas.

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