PAR6, a potential marker for the germ cells selected to form primordial follicles in mouse ovary.

Partitioning-defective proteins (PAR) are detected to express mainly in the cytoplast, and play an important role in cell polarity. However, we showed here that PAR6, one kind of PAR protein, was localized in the nuclei of mouse oocytes that formed primordial follicles during the perinatal period, s...

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Main Authors: Jing Wen, Hua Zhang, Ge Li, Guanping Mao, Xiufen Chen, Jianwei Wang, Meng Guo, Xinyi Mu, Hong Ouyang, Meijia Zhang, Guoliang Xia
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-10-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2753645?pdf=render
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spelling doaj-3b7732c95ec047bf88f2fda8fd392da02020-11-24T21:52:04ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-10-01410e737210.1371/journal.pone.0007372PAR6, a potential marker for the germ cells selected to form primordial follicles in mouse ovary.Jing WenHua ZhangGe LiGuanping MaoXiufen ChenJianwei WangMeng GuoXinyi MuHong OuyangMeijia ZhangGuoliang XiaPartitioning-defective proteins (PAR) are detected to express mainly in the cytoplast, and play an important role in cell polarity. However, we showed here that PAR6, one kind of PAR protein, was localized in the nuclei of mouse oocytes that formed primordial follicles during the perinatal period, suggesting a new role of PAR protein. It is the first time we found that, in mouse fetal ovaries, PAR6 appeared in somatic cell cytoplasm and fell weak when somatic cells invaded germ cell cysts at 17.5 days post coitus (dpc). Meanwhile, the expression of PAR6 was observed in cysts, and became strong in the nuclei of some germ cells at 19.5 dpc and all primordial follicular oocytes at 3 day post parturition (dpp), and then obviously declined when the primordial follicles entered the folliculogenic growth phase. During the primordial follicle pool foundation, the number of PAR6 positive germ cells remained steady and was consistent with that of formed follicles at 3 dpp. There were no TUNEL (apoptosis examination) positive germ cells stained with PAR6 at any time studied. The number of follicles significantly declined when 15.5 dpc ovaries were treated with the anti-PAR6 antibody and PAR6 RNA interference. Carbenoxolone (CBX, a known blocker of gap junctions) inhibited the expression of PAR6 in germ cells and the formation of follicles. Our results suggest that PAR6 could be used as a potential marker of germ cells for the primordial follicle formation, and the expression of PAR6 by a gap junction-dependent process may contribute to the formation of primordial follicles and the maintenance of oocytes at the diplotene stage.http://europepmc.org/articles/PMC2753645?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jing Wen
Hua Zhang
Ge Li
Guanping Mao
Xiufen Chen
Jianwei Wang
Meng Guo
Xinyi Mu
Hong Ouyang
Meijia Zhang
Guoliang Xia
spellingShingle Jing Wen
Hua Zhang
Ge Li
Guanping Mao
Xiufen Chen
Jianwei Wang
Meng Guo
Xinyi Mu
Hong Ouyang
Meijia Zhang
Guoliang Xia
PAR6, a potential marker for the germ cells selected to form primordial follicles in mouse ovary.
PLoS ONE
author_facet Jing Wen
Hua Zhang
Ge Li
Guanping Mao
Xiufen Chen
Jianwei Wang
Meng Guo
Xinyi Mu
Hong Ouyang
Meijia Zhang
Guoliang Xia
author_sort Jing Wen
title PAR6, a potential marker for the germ cells selected to form primordial follicles in mouse ovary.
title_short PAR6, a potential marker for the germ cells selected to form primordial follicles in mouse ovary.
title_full PAR6, a potential marker for the germ cells selected to form primordial follicles in mouse ovary.
title_fullStr PAR6, a potential marker for the germ cells selected to form primordial follicles in mouse ovary.
title_full_unstemmed PAR6, a potential marker for the germ cells selected to form primordial follicles in mouse ovary.
title_sort par6, a potential marker for the germ cells selected to form primordial follicles in mouse ovary.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2009-10-01
description Partitioning-defective proteins (PAR) are detected to express mainly in the cytoplast, and play an important role in cell polarity. However, we showed here that PAR6, one kind of PAR protein, was localized in the nuclei of mouse oocytes that formed primordial follicles during the perinatal period, suggesting a new role of PAR protein. It is the first time we found that, in mouse fetal ovaries, PAR6 appeared in somatic cell cytoplasm and fell weak when somatic cells invaded germ cell cysts at 17.5 days post coitus (dpc). Meanwhile, the expression of PAR6 was observed in cysts, and became strong in the nuclei of some germ cells at 19.5 dpc and all primordial follicular oocytes at 3 day post parturition (dpp), and then obviously declined when the primordial follicles entered the folliculogenic growth phase. During the primordial follicle pool foundation, the number of PAR6 positive germ cells remained steady and was consistent with that of formed follicles at 3 dpp. There were no TUNEL (apoptosis examination) positive germ cells stained with PAR6 at any time studied. The number of follicles significantly declined when 15.5 dpc ovaries were treated with the anti-PAR6 antibody and PAR6 RNA interference. Carbenoxolone (CBX, a known blocker of gap junctions) inhibited the expression of PAR6 in germ cells and the formation of follicles. Our results suggest that PAR6 could be used as a potential marker of germ cells for the primordial follicle formation, and the expression of PAR6 by a gap junction-dependent process may contribute to the formation of primordial follicles and the maintenance of oocytes at the diplotene stage.
url http://europepmc.org/articles/PMC2753645?pdf=render
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