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本文引用的文献

1
Expression of stimulated by retinoic acid gene 8 (Stra8) and maturation of murine gonocytes and spermatogonia induced by retinoic acid in vitro.视黄酸诱导基因8(Stra8)的表达以及视黄酸在体外诱导小鼠生殖母细胞和精原细胞的成熟
Biol Reprod. 2008 Mar;78(3):537-45. doi: 10.1095/biolreprod.107.064337. Epub 2007 Nov 21.
2
In germ cells of mouse embryonic ovaries, the decision to enter meiosis precedes premeiotic DNA replication.在小鼠胚胎卵巢的生殖细胞中,进入减数分裂的决定先于减数分裂前的DNA复制。
Nat Genet. 2006 Dec;38(12):1430-4. doi: 10.1038/ng1919. Epub 2006 Nov 19.
3
Identifying genes important for spermatogonial stem cell self-renewal and survival.鉴定对精原干细胞自我更新和存活至关重要的基因。
Proc Natl Acad Sci U S A. 2006 Jun 20;103(25):9524-9. doi: 10.1073/pnas.0603332103. Epub 2006 Jun 1.
4
Retinoid signaling determines germ cell fate in mice.维甲酸信号通路决定小鼠生殖细胞的命运。
Science. 2006 Apr 28;312(5773):596-600. doi: 10.1126/science.1125691. Epub 2006 Mar 30.
5
Spermatogonial stem cells: characteristics and experimental possibilities.精原干细胞:特性与实验可能性
APMIS. 2005 Nov-Dec;113(11-12):727-42. doi: 10.1111/j.1600-0463.2005.apm_302.x.
6
Retinoic acid regulates sex-specific timing of meiotic initiation in mice.视黄酸调节小鼠减数分裂起始的性别特异性时间。
Proc Natl Acad Sci U S A. 2006 Feb 21;103(8):2474-9. doi: 10.1073/pnas.0510813103. Epub 2006 Feb 6.
7
Stem cell protein Piwil2 modulates expression of murine spermatogonial stem cell expressed genes.干细胞蛋白Piwil2调节小鼠精原干细胞表达基因的表达。
Mol Reprod Dev. 2006 Feb;73(2):173-9. doi: 10.1002/mrd.20391.
8
Preparation, isolation and characterization of stage-specific spermatogenic cells for cellular and molecular analysis.用于细胞和分子分析的阶段特异性生精细胞的制备、分离及特性鉴定
Nat Methods. 2004 Dec;1(3):249-54. doi: 10.1038/nmeth1204-249.
9
Maintenance of spermatogenesis requires TAF4b, a gonad-specific subunit of TFIID.精子发生的维持需要TAF4b,它是TFIID的一个性腺特异性亚基。
Genes Dev. 2005 Apr 1;19(7):794-803. doi: 10.1101/gad.1290105. Epub 2005 Mar 17.
10
Androgen-regulated transcripts in the neonatal mouse testis as determined through microarray analysis.通过微阵列分析确定的新生小鼠睾丸中的雄激素调节转录本。
Biol Reprod. 2005 Apr;72(4):1010-9. doi: 10.1095/biolreprod.104.035915. Epub 2004 Dec 15.

视黄酸诱导的生精细胞中视黄酸基因8(Stra8)的表达:维生素A充足的出生后小鼠睾丸的体内研究

Expression of stimulated by retinoic acid gene 8 (Stra8) in spermatogenic cells induced by retinoic acid: an in vivo study in vitamin A-sufficient postnatal murine testes.

作者信息

Zhou Qing, Nie Rong, Li Ying, Friel Patrick, Mitchell Debra, Hess Rex A, Small Christopher, Griswold Michael D

机构信息

School of Molecular Biosciences, Washington State University, Pullman, Washington 99164-4660, USA.

出版信息

Biol Reprod. 2008 Jul;79(1):35-42. doi: 10.1095/biolreprod.107.066795. Epub 2008 Mar 5.

DOI:10.1095/biolreprod.107.066795
PMID:18322276
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3208264/
Abstract

Vitamin A is required for male fertility and normal spermatogenesis. Retinoic acid (RA), an active metabolite of vitamin A, is necessary for spermatogonial maturation and proper entry of germ cells into meiotic prophase in the postnatal testes. The expression of Stra8, which is essential for successful meiosis in both male and female gonads and normal spermatogenesis, is directly related to the availability of RA. This study examined the developmental expression pattern of Stra8 transcript in both male and female gonads, provided specific cellular localization of STRA8 protein in the postnatal and adult testis, and investigated RA actions in adult germ cells in a vitamin A-sufficient condition. The peak of Stra8 mRNA expression coincided with the onset of meiosis in postnatal testes. STRA8 protein was detected in gonocytes as early as 5 days postpartum. The expression of STRA8 protein in the neonatal testes was not uniform among spermatogonia, perhaps heralding the asynchronous beginning of spermatogenesis. In adult testes, the highest level of Stra8 mRNA and protein was found in seminiferous epithelial stages VI-VIII. STRA8 protein was localized to some type A and B spermatogonia, preleptotene spermatocytes, and early leptotene spermatocytes. In the vitamin A-sufficient adult testes, RA but not retinol acetate stimulated Stra8 mRNA expression. STRA8 protein expression in adult spermatogonia was induced by RA stimulation, suggesting its role in spermatogonial differentiation. Retinoic acid also increased the number of preleptotene spermatocytes exhibiting 5-bromo-2-deoxyuridine incorporation, indicating a more synchronized premeiotic DNA replication.

摘要

维生素A对男性生育能力和正常精子发生是必需的。视黄酸(RA)是维生素A的一种活性代谢产物,对于生精细胞成熟以及出生后睾丸中生殖细胞正常进入减数分裂前期是必需的。Stra8的表达对于雄性和雌性性腺的成功减数分裂以及正常精子发生至关重要,它与RA的可利用性直接相关。本研究检测了Stra8转录本在雄性和雌性性腺中的发育表达模式,提供了STRA8蛋白在出生后和成年睾丸中的特定细胞定位,并研究了在维生素A充足条件下RA在成年生殖细胞中的作用。Stra8 mRNA表达的峰值与出生后睾丸减数分裂的开始时间一致。早在产后5天就在生殖母细胞中检测到了STRA8蛋白。STRA8蛋白在新生睾丸生精细胞中的表达并不均匀,这可能预示着精子发生的异步开始。在成年睾丸中,Stra8 mRNA和蛋白的最高水平出现在生精上皮的VI-VIII期。STRA8蛋白定位于一些A型和B型生精细胞、前细线期精母细胞和早期细线期精母细胞。在维生素A充足的成年睾丸中,RA而非醋酸视黄醇刺激了Stra8 mRNA的表达。RA刺激诱导了成年生精细胞中STRA8蛋白的表达,表明其在生精细胞分化中的作用。视黄酸还增加了显示5-溴-2-脱氧尿苷掺入的前细线期精母细胞的数量,表明减数分裂前DNA复制更加同步。