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E4转录因子1(E4F1)调节小鼠睾丸支持细胞增殖和生育能力。

E4 Transcription Factor 1 (E4F1) Regulates Sertoli Cell Proliferation and Fertility in Mice.

作者信息

Yan Rong-Ge, Yang Qi-Lin, Yang Qi-En

机构信息

Key Laboratory of Adaptation and Evolution of Plateau Biota, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining 810000, China.

College of Life Science, University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

Animals (Basel). 2020 Sep 18;10(9):1691. doi: 10.3390/ani10091691.

Abstract

In the mammalian testes, Sertoli cells are the only somatic cells in the seminiferous tubules that provide structural, nutritional and regulatory support for developing spermatogenic cells. Sertoli cells only proliferate during the fetal and neonatal periods and enter a quiescent state after puberty. Functional evidences suggest that the size of Sertoli cell population determines sperm production and fertility. However, factors that direct Sertoli cell proliferation and maturation are not fully understood. Transcription factor E4F1 is a multifunctional protein that serves essential roles in cell fate decisions and because it interacts with pRB, a master regulator of Sertoli cell function, we hypothesized that E4F1 may have a functional role in Sertoli cells. mRNA was present in murine testis and immunohistochemical staining confirmed that E4F1 was enriched in mature Sertoli cells. We generated a conditional knockout mouse model using and lines to study E4F1 fucntion in Sertoli cells and the results showed that deletion caused a significant reduction in testis size and fertility. Further analyses revealed that meiosis progression and spermiogenesis were normal, however, Sertoli cell proliferation was impaired and germ cell apoptosis was elevated in the testis of conditional knockout mice. On the basis of these findings, we concluded that E4F1 was expressed in murine Sertoli cells and served important functions in regulating Sertoli cell proliferation and fertility.

摘要

在哺乳动物睾丸中,支持细胞是生精小管中唯一的体细胞,为发育中的生精细胞提供结构、营养和调节支持。支持细胞仅在胎儿期和新生儿期增殖,青春期后进入静止状态。功能证据表明,支持细胞群体的大小决定精子生成和生育能力。然而,指导支持细胞增殖和成熟的因素尚未完全了解。转录因子E4F1是一种多功能蛋白,在细胞命运决定中起重要作用,并且由于它与支持细胞功能的主要调节因子pRB相互作用,我们推测E4F1可能在支持细胞中具有功能作用。mRNA存在于小鼠睾丸中,免疫组织化学染色证实E4F1在成熟支持细胞中富集。我们使用 和 品系生成了一个条件性敲除小鼠模型,以研究E4F1在支持细胞中的功能,结果表明 缺失导致睾丸大小和生育能力显著降低。进一步分析显示,减数分裂进程和精子发生正常,然而,在 条件性敲除小鼠的睾丸中,支持细胞增殖受损,生殖细胞凋亡增加。基于这些发现,我们得出结论,E4F1在小鼠支持细胞中表达,并在调节支持细胞增殖和生育能力方面发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b74/7552733/4eb8e0191561/animals-10-01691-g001.jpg

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