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本文引用的文献

1
Single-cell RNAseq analysis of testicular germ and somatic cell development during the perinatal period.围生期睾丸生殖细胞和体细胞发育的单细胞 RNA 测序分析。
Development. 2020 Feb 3;147(3):dev183251. doi: 10.1242/dev.183251.
2
Mammalian germ cells are determined after PGC colonization of the nascent gonad.哺乳动物生殖细胞在原始性腺中被原始生殖细胞定植后就被决定了。
Proc Natl Acad Sci U S A. 2019 Dec 17;116(51):25677-25687. doi: 10.1073/pnas.1910733116. Epub 2019 Nov 21.
3
Developmental kinetics and transcriptome dynamics of stem cell specification in the spermatogenic lineage.生精谱系中干细胞特化的发育动力学和转录组动力学。
Nat Commun. 2019 Jun 26;10(1):2787. doi: 10.1038/s41467-019-10596-0.
4
Identification of EOMES-expressing spermatogonial stem cells and their regulation by PLZF.鉴定表达 EOMES 的精原干细胞及其受 PLZF 的调控。
Elife. 2019 May 31;8:e43352. doi: 10.7554/eLife.43352.
5
Differential RA responsiveness directs formation of functionally distinct spermatogonial populations at the initiation of spermatogenesis in the mouse.在小鼠精子发生起始时,差异的 RA 反应性指导功能不同的精原细胞群体的形成。
Development. 2019 May 13;146(12):dev173088. doi: 10.1242/dev.173088.
6
Single cell RNA-sequencing identified Dec2 as a suppressive factor for spermatogonial differentiation by inhibiting Sohlh1 expression.单细胞 RNA 测序鉴定出 Dec2 是通过抑制 Sohlh1 表达来抑制精原细胞分化的抑制因子。
Sci Rep. 2019 Apr 15;9(1):6063. doi: 10.1038/s41598-019-42578-z.
7
Dynamic transcriptome profiles within spermatogonial and spermatocyte populations during postnatal testis maturation revealed by single-cell sequencing.单细胞测序揭示了出生后睾丸成熟过程中精原细胞和精母细胞群体中的动态转录组谱。
PLoS Genet. 2019 Mar 20;15(3):e1007810. doi: 10.1371/journal.pgen.1007810. eCollection 2019 Mar.
8
The Neonatal and Adult Human Testis Defined at the Single-Cell Level.单细胞水平定义的新生儿和成人睾丸。
Cell Rep. 2019 Feb 5;26(6):1501-1517.e4. doi: 10.1016/j.celrep.2019.01.045.
9
The adult human testis transcriptional cell atlas.成人睾丸转录组细胞图谱。
Cell Res. 2018 Dec;28(12):1141-1157. doi: 10.1038/s41422-018-0099-2. Epub 2018 Oct 12.
10
Purification of GFRα1+ and GFRα1- Spermatogonial Stem Cells Reveals a Niche-Dependent Mechanism for Fate Determination.GFRα1+ 和 GFRα1- 精原干细胞的纯化揭示了命运决定的龛依赖性机制。
Stem Cell Reports. 2018 Feb 13;10(2):553-567. doi: 10.1016/j.stemcr.2017.12.009. Epub 2018 Jan 11.

精原干细胞建立的发育基础。

Developmental underpinnings of spermatogonial stem cell establishment.

机构信息

Center for Reproductive Biology, School of Molecular Biosciences, College of Veterinary Medicine, Washington State University, Pullman, WA, USA.

出版信息

Andrology. 2020 Jul;8(4):852-861. doi: 10.1111/andr.12810. Epub 2020 May 24.

DOI:10.1111/andr.12810
PMID:32356598
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8324036/
Abstract

BACKGROUND

The germline serves as a conduit for transmission of genetic and epigenetic information from one generation to the next. In males, spermatozoa are the final carriers of inheritance and their continual production is supported by a foundational population of spermatogonial stem cells (SSCs) that forms from prospermatogonial precursors during the early stages of neonatal development. In mammals, the timing for which SSCs are specified and the underlying mechanisms guiding this process remain to be completely understood.

OBJECTIVES

To propose an evolving concept for how the foundational SSC population is established.

MATERIALS AND METHODS

This review summarizes recent and historical findings from peer-reviewed publications made primarily with mouse models while incorporating limited studies from humans and livestock.

RESULTS AND CONCLUSION

Establishment of the SSC population appears to follow a biphasic pattern involving a period of fate programming followed by an establishment phase that culminates in formation of the SSC population. This model for establishment of the foundational SSC population from precursors is anticipated to extend across mammalian species and include humans and livestock, albeit on different timescales.

摘要

背景

种系作为遗传和表观遗传信息从一代传递到下一代的通道。在男性中,精子是遗传的最终载体,其持续产生由新生儿发育早期的前生殖细胞祖细胞形成的基础精原干细胞(SSC)群体支持。在哺乳动物中,SSC 被指定的时间以及指导这一过程的潜在机制仍有待完全理解。

目的

提出一个关于基础 SSC 群体如何建立的发展概念。

材料和方法

本综述总结了主要使用小鼠模型的同行评审出版物中的最新和历史发现,同时纳入了来自人类和家畜的有限研究。

结果和结论

SSC 群体的建立似乎遵循双相模式,包括一个命运编程期,随后是一个建立期,最终形成 SSC 群体。这种从前体建立基础 SSC 群体的模型预计将扩展到哺乳动物物种,包括人类和家畜,但时间尺度不同。