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CD2 is a surface marker for mouse and rat spermatogonial stem cells

The spermatogonial stem cell (SSC) population in testis is small, and the lack of SSC markers has severely handicapped research on these cells. During our attempt to identify genes involved in SSC aging, we found that CD2 is expressed in cultured SSCs. Flow cytometric analysis and spermatogonial tra...

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Autores principales: KANATSU-SHINOHARA, Mito, CHEN, Guiying, MORIMOTO, Hiroko, SHINOHARA, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Society for Reproduction and Development 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7470899/
https://www.ncbi.nlm.nih.gov/pubmed/32213736
http://dx.doi.org/10.1262/jrd.2020-019
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author KANATSU-SHINOHARA, Mito
CHEN, Guiying
MORIMOTO, Hiroko
SHINOHARA, Takashi
author_facet KANATSU-SHINOHARA, Mito
CHEN, Guiying
MORIMOTO, Hiroko
SHINOHARA, Takashi
author_sort KANATSU-SHINOHARA, Mito
collection PubMed
description The spermatogonial stem cell (SSC) population in testis is small, and the lack of SSC markers has severely handicapped research on these cells. During our attempt to identify genes involved in SSC aging, we found that CD2 is expressed in cultured SSCs. Flow cytometric analysis and spermatogonial transplantation experiments showed that CD2 is expressed in SSCs from mature adult mouse testes. Cultured SSCs transfected with short hairpin RNAs (shRNAs) against CD2 proliferated poorly and showed an increased frequency of apoptosis. Moreover, functional analysis of transfected cells revealed impairment of SSC activity. Fluorescence activated cell sorting and spermatogonial transplantation experiments showed that CD2 is expressed not only in mouse but also in rat SSCs. The results indicate that CD2 is a novel SSC surface marker conserved between mouse and rat SSCs.
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spelling pubmed-74708992020-09-09 CD2 is a surface marker for mouse and rat spermatogonial stem cells KANATSU-SHINOHARA, Mito CHEN, Guiying MORIMOTO, Hiroko SHINOHARA, Takashi J Reprod Dev Original Article The spermatogonial stem cell (SSC) population in testis is small, and the lack of SSC markers has severely handicapped research on these cells. During our attempt to identify genes involved in SSC aging, we found that CD2 is expressed in cultured SSCs. Flow cytometric analysis and spermatogonial transplantation experiments showed that CD2 is expressed in SSCs from mature adult mouse testes. Cultured SSCs transfected with short hairpin RNAs (shRNAs) against CD2 proliferated poorly and showed an increased frequency of apoptosis. Moreover, functional analysis of transfected cells revealed impairment of SSC activity. Fluorescence activated cell sorting and spermatogonial transplantation experiments showed that CD2 is expressed not only in mouse but also in rat SSCs. The results indicate that CD2 is a novel SSC surface marker conserved between mouse and rat SSCs. The Society for Reproduction and Development 2020-03-26 2020-08 /pmc/articles/PMC7470899/ /pubmed/32213736 http://dx.doi.org/10.1262/jrd.2020-019 Text en ©2020 Society for Reproduction and Development This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Original Article
KANATSU-SHINOHARA, Mito
CHEN, Guiying
MORIMOTO, Hiroko
SHINOHARA, Takashi
CD2 is a surface marker for mouse and rat spermatogonial stem cells
title CD2 is a surface marker for mouse and rat spermatogonial stem cells
title_full CD2 is a surface marker for mouse and rat spermatogonial stem cells
title_fullStr CD2 is a surface marker for mouse and rat spermatogonial stem cells
title_full_unstemmed CD2 is a surface marker for mouse and rat spermatogonial stem cells
title_short CD2 is a surface marker for mouse and rat spermatogonial stem cells
title_sort cd2 is a surface marker for mouse and rat spermatogonial stem cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7470899/
https://www.ncbi.nlm.nih.gov/pubmed/32213736
http://dx.doi.org/10.1262/jrd.2020-019
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