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体内基因向睾丸和精子的转移:进展与未来应用。

In vivo gene transfer into testis and sperm: developments and future application.

作者信息

Coward Kevin, Kubota Hiroki, Parrington John

机构信息

Department of Pharmacology, University of Oxford, Oxford, UK.

出版信息

Arch Androl. 2007 Jul-Aug;53(4):187-97. doi: 10.1080/01485010701426455.

Abstract

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.

摘要

尽管通过辅助生殖技术(ART)治疗不孕症取得了重大进展,但特发性男性不育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紊乱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,有必要在雄性生殖细胞中操纵基因表达。由于仍然没有可靠的方法来重现精子发生培养,因此在睾丸和精子的基因功能研究中,开发替代的转基因方法至关重要。创建转基因动物的既定方法严重依赖于将DNA注入原核或将转染的胚胎干细胞注入囊胚以形成嵌合体。尽管这两种制造转基因和基因敲除动物的方法取得了成功,但人们仍然担心成本和转基因整合的效率。因此,正在努力评估替代方法。目前,人们对开发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),作为不孕症研究和创建转基因动物的工具具有巨大潜力。这篇简短综述的目的是简要描述该领域的发展,并讨论这些基因转移方法如何在未来的研究和临床领域中有效应用。

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