The pluripotency factor LIN28 marks undifferentiated spermatogonia in mouse

<p>Abstract</p> <p>Background</p> <p>Life-long production of spermatozoa depends on spermatogonial stem cells. Spermatogonial stem cells exist among the most primitive population of germ cells – undifferentiated spermatogonia. Transplantation experiments have demonstrat...

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Main Authors: Kaestner Klaus H, Wu Xin, Zheng Ke, Wang Peijing
Format: Article
Language:English
Published: BMC 2009-06-01
Series:BMC Developmental Biology
Online Access:http://www.biomedcentral.com/1471-213X/9/38
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spelling doaj-531bcd85fd074169828c4d2fd21933bc2020-11-24T21:44:55ZengBMCBMC Developmental Biology1471-213X2009-06-01913810.1186/1471-213X-9-38The pluripotency factor LIN28 marks undifferentiated spermatogonia in mouseKaestner Klaus HWu XinZheng KeWang Peijing<p>Abstract</p> <p>Background</p> <p>Life-long production of spermatozoa depends on spermatogonial stem cells. Spermatogonial stem cells exist among the most primitive population of germ cells – undifferentiated spermatogonia. Transplantation experiments have demonstrated the functional heterogeneity of undifferentiated spermatogonia. Although the undifferentiated spermatogonia can be topographically divided into A<sub>s </sub>(single), A<sub>pr </sub>(paired), and A<sub>al </sub>(aligned) spermatogonia, subdivision of this primitive cell population using cytological markers would greatly facilitate characterization of their functions.</p> <p>Results</p> <p>In the present study, we show that LIN28, a pluripotency factor, is specifically expressed in undifferentiated spermatogonia (A<sub>s</sub>, A<sub>pr</sub>, and A<sub>al</sub>) in mouse. <it>Ngn3 </it>also specifically labels undifferentiated spermatogonia. We used <it>Ngn3</it>-GFP knockin mice, in which GFP expression is under the control of all <it>Ngn3 </it>transcription regulatory elements. Remarkably, <it>Ngn3</it>-GFP is only expressed in ~40% of LIN28-positive A<sub>s </sub>(single) cells. The percentage of <it>Ngn3</it>-GFP-positive clusters increases dramatically with the chain length of interconnected spermatogonia.</p> <p>Conclusion</p> <p>Our study demonstrates that LIN28 specifically marks undifferentiated spermatogonia in mice. These data, together with previous studies, suggest that the LIN28-expressing undifferentiated spermatogonia exist as two subpopulations: <it>Ngn3</it>-GFP-negative (high stem cell potential) and <it>Ngn3</it>-GFP-positive (high differentiation commitment). Furthermore, <it>Ngn3</it>-GFP-negative cells are found in chains of <it>Ngn3</it>-GFP-positive spermatogonia, suggesting that cells in the A<sub>al </sub>spermatogonia could revert to a more primitive state.</p> http://www.biomedcentral.com/1471-213X/9/38
collection DOAJ
language English
format Article
sources DOAJ
author Kaestner Klaus H
Wu Xin
Zheng Ke
Wang Peijing
spellingShingle Kaestner Klaus H
Wu Xin
Zheng Ke
Wang Peijing
The pluripotency factor LIN28 marks undifferentiated spermatogonia in mouse
BMC Developmental Biology
author_facet Kaestner Klaus H
Wu Xin
Zheng Ke
Wang Peijing
author_sort Kaestner Klaus H
title The pluripotency factor LIN28 marks undifferentiated spermatogonia in mouse
title_short The pluripotency factor LIN28 marks undifferentiated spermatogonia in mouse
title_full The pluripotency factor LIN28 marks undifferentiated spermatogonia in mouse
title_fullStr The pluripotency factor LIN28 marks undifferentiated spermatogonia in mouse
title_full_unstemmed The pluripotency factor LIN28 marks undifferentiated spermatogonia in mouse
title_sort pluripotency factor lin28 marks undifferentiated spermatogonia in mouse
publisher BMC
series BMC Developmental Biology
issn 1471-213X
publishDate 2009-06-01
description <p>Abstract</p> <p>Background</p> <p>Life-long production of spermatozoa depends on spermatogonial stem cells. Spermatogonial stem cells exist among the most primitive population of germ cells – undifferentiated spermatogonia. Transplantation experiments have demonstrated the functional heterogeneity of undifferentiated spermatogonia. Although the undifferentiated spermatogonia can be topographically divided into A<sub>s </sub>(single), A<sub>pr </sub>(paired), and A<sub>al </sub>(aligned) spermatogonia, subdivision of this primitive cell population using cytological markers would greatly facilitate characterization of their functions.</p> <p>Results</p> <p>In the present study, we show that LIN28, a pluripotency factor, is specifically expressed in undifferentiated spermatogonia (A<sub>s</sub>, A<sub>pr</sub>, and A<sub>al</sub>) in mouse. <it>Ngn3 </it>also specifically labels undifferentiated spermatogonia. We used <it>Ngn3</it>-GFP knockin mice, in which GFP expression is under the control of all <it>Ngn3 </it>transcription regulatory elements. Remarkably, <it>Ngn3</it>-GFP is only expressed in ~40% of LIN28-positive A<sub>s </sub>(single) cells. The percentage of <it>Ngn3</it>-GFP-positive clusters increases dramatically with the chain length of interconnected spermatogonia.</p> <p>Conclusion</p> <p>Our study demonstrates that LIN28 specifically marks undifferentiated spermatogonia in mice. These data, together with previous studies, suggest that the LIN28-expressing undifferentiated spermatogonia exist as two subpopulations: <it>Ngn3</it>-GFP-negative (high stem cell potential) and <it>Ngn3</it>-GFP-positive (high differentiation commitment). Furthermore, <it>Ngn3</it>-GFP-negative cells are found in chains of <it>Ngn3</it>-GFP-positive spermatogonia, suggesting that cells in the A<sub>al </sub>spermatogonia could revert to a more primitive state.</p>
url http://www.biomedcentral.com/1471-213X/9/38
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