Suppr超能文献

视黄酸受体A在精子发生过程中对支持细胞和生殖细胞的潜在作用。

Potential functions of retinoic acid receptor A in Sertoli cells and germ cells during spermatogenesis.

作者信息

Doyle Timothy J, Braun Kirt W, McLean Derek J, Wright Raymond W, Griswold Michael D, Kim Kwan Hee

机构信息

School of Molecular Biosciences, Washington State University, Pullman, WA 99164-4234, USA.

出版信息

Ann N Y Acad Sci. 2007 Dec;1120:114-30. doi: 10.1196/annals.1411.008. Epub 2007 Sep 28.

Abstract

Elucidation of the retinoid signaling circuitry in the testis is critical to understanding how male germ cells develop to spermatozoa. Retinoic acid receptor A protein (RARA) is an essential mediator of retinoid signaling in the testis, as shown by a sterility phenotype observed for retinoic acid receptor A gene (Rara) knockout male mice. The seminiferous tubules of Rara knockout mice showed varying degrees of germ-cell degeneration. A dramatic increase in apoptosis of early meiotic prophase spermatocytes was observed in these tubules compared to the wild-type tubules. Germ-cell loss was dependent on the stages of the spermatogenic cycle: germ-cell loss was negligible in stages I-V, but severe after stages VIII and IX of the spermatogenic cycle. Using spermatogonial transplantation, the individual function of RARA in Sertoli cells or germ cells was determined. The wild-type donor germ cells, transplanted into Rara knockout testes, colonized and proliferated in the RARA-deficient microenvironment. The donor-derived cells were mostly early meiotic prophase spermatocytes, with few more advanced germ cells detected. Conversely, when Rara-deficient germ cells were injected into the microenvironment that express RARA, establishment of donor-derived germ-cell colonies was rare, but remarkably, once colonized, Rara-deficient germ cells progressed normally through spermatogenesis. These results together suggest that RARA may function in Sertoli cells to promote the survival and development of early meiotic prophase spermatocytes, whereas RARA in germ cells functions to increase the proliferation and differentiation of spermatogonia, prior to meiotic prophase.

摘要

阐明睾丸中的视黄酸信号传导通路对于理解雄性生殖细胞如何发育成精子至关重要。视黄酸受体A蛋白(RARA)是睾丸中视黄酸信号传导的重要介质,视黄酸受体A基因(Rara)敲除的雄性小鼠出现的不育表型证明了这一点。Rara敲除小鼠的生精小管显示出不同程度的生殖细胞退化。与野生型小管相比,在这些小管中观察到减数分裂前期早期精母细胞的凋亡显著增加。生殖细胞的丢失取决于生精周期的阶段:在I-V阶段生殖细胞丢失可忽略不计,但在生精周期的VIII和IX阶段之后则很严重。利用精原细胞移植,确定了RARA在支持细胞或生殖细胞中的个体功能。将野生型供体生殖细胞移植到Rara敲除的睾丸中,它们在缺乏RARA的微环境中定植并增殖。供体来源的细胞大多是减数分裂前期早期精母细胞,检测到的更晚期生殖细胞很少。相反,当将缺乏Rara的生殖细胞注射到表达RARA的微环境中时,供体来源的生殖细胞集落的建立很少见,但值得注意的是,一旦定植,缺乏Rara的生殖细胞在精子发生过程中正常进展。这些结果共同表明,RARA可能在支持细胞中发挥作用,以促进减数分裂前期早期精母细胞的存活和发育,而生殖细胞中的RARA在减数分裂前期之前发挥作用,以增加精原细胞的增殖和分化。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验