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本文引用的文献

1
Decline in self-renewal factors contributes to aging of the stem cell niche in the Drosophila testis.自我更新因子的减少导致果蝇睾丸中干细胞微环境的老化。
Cell Stem Cell. 2007 Oct 11;1(4):470-8. doi: 10.1016/j.stem.2007.08.002.
2
The missing niche for spermatogonial stem cells: do blood vessels point the way?精原干细胞缺失的生态位:血管能指明方向吗?
Cell Stem Cell. 2007 Oct 11;1(4):361-3. doi: 10.1016/j.stem.2007.09.013.
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Transcriptome analysis of differentiating spermatogonia stimulated with kit ligand.用干细胞因子刺激分化中的精原细胞的转录组分析
Gene Expr Patterns. 2008 Jan;8(2):58-70. doi: 10.1016/j.modgep.2007.10.007. Epub 2007 Oct 25.
4
Gdnf upregulates c-Fos transcription via the Ras/Erk1/2 pathway to promote mouse spermatogonial stem cell proliferation.胶质细胞源性神经营养因子(Gdnf)通过Ras/Erk1/2信号通路上调c-Fos转录,以促进小鼠精原干细胞增殖。
Stem Cells. 2008 Jan;26(1):266-78. doi: 10.1634/stemcells.2007-0436. Epub 2007 Oct 25.
5
ETV5 is required for continuous spermatogenesis in adult mice and may mediate blood testes barrier function and testicular immune privilege.ETV5是成年小鼠持续精子发生所必需的,并且可能介导血睾屏障功能和睾丸免疫豁免。
Ann N Y Acad Sci. 2007 Dec;1120:144-51. doi: 10.1196/annals.1411.005. Epub 2007 Oct 2.
6
A vasculature-associated niche for undifferentiated spermatogonia in the mouse testis.小鼠睾丸中未分化精原细胞的血管相关微环境。
Science. 2007 Sep 21;317(5845):1722-6. doi: 10.1126/science.1144885. Epub 2007 Sep 6.
7
Repression of kit expression by Plzf in germ cells.在生殖细胞中,Plzf对kit表达的抑制作用。
Mol Cell Biol. 2007 Oct;27(19):6770-81. doi: 10.1128/MCB.00479-07. Epub 2007 Jul 30.
8
Glial cell line-derived neurotrophic factor regulation of genes essential for self-renewal of mouse spermatogonial stem cells is dependent on Src family kinase signaling.胶质细胞系源性神经营养因子对小鼠精原干细胞自我更新所必需基因的调控依赖于Src家族激酶信号传导。
J Biol Chem. 2007 Aug 31;282(35):25842-51. doi: 10.1074/jbc.M703474200. Epub 2007 Jun 27.
9
Common and distinct factors regulate expression of mRNA for ETV5 and GDNF, Sertoli cell proteins essential for spermatogonial stem cell maintenance.共同和独特的因素调节ETV5和GDNF(对精原干细胞维持至关重要的支持细胞蛋白)的mRNA表达。
Exp Cell Res. 2007 Aug 15;313(14):3090-9. doi: 10.1016/j.yexcr.2007.05.002. Epub 2007 May 10.
10
Akt mediates self-renewal division of mouse spermatogonial stem cells.Akt介导小鼠精原干细胞的自我更新分裂。
Development. 2007 May;134(10):1853-9. doi: 10.1242/dev.003004. Epub 2007 Apr 11.

精原干细胞微环境的调控。

Regulation of the spermatogonial stem cell niche.

作者信息

Kostereva N, Hofmann M-C

机构信息

Department of Veterinary Biosciences, University of Illinois at Urbana-Champaign, Urbana, IL 61802, USA.

出版信息

Reprod Domest Anim. 2008 Jul;43 Suppl 2(Suppl 2):386-92. doi: 10.1111/j.1439-0531.2008.01189.x.

DOI:10.1111/j.1439-0531.2008.01189.x
PMID:18638151
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2904914/
Abstract

Spermatogonial stem cells (SSCs) reside within specialized microenvironments called 'niches', which are essential for their maintenance and self-renewal. In the mammalian testis, the main components of the niche include the Sertoli cell, the growth factors that this nursing cell produces, the basement membrane, and stimuli from the vascular network between the seminiferous tubules. This review focuses on signalling pathways maintaining SSCs self-renewal and differentiation and describes potential mechanisms of regulation of the spermatogonial stem cell niche.

摘要

精原干细胞(SSCs)存在于被称为“龛”的特殊微环境中,这对其维持和自我更新至关重要。在哺乳动物睾丸中,龛的主要组成部分包括支持细胞、该滋养细胞产生的生长因子、基底膜以及来自生精小管之间血管网络的刺激。本综述重点关注维持SSCs自我更新和分化的信号通路,并描述精原干细胞龛的潜在调控机制。