Histone acetylase inhibitor curcumin impairs mouse spermiogenesis-an in vitro study.

In the previous study, we unraveled the unique "erasure strategy" during the mouse spermiogenesis. Chromatin associated proteins sequentially disassociated from the spermatid chromosome, which led to the termination of transcription in elongating spermatids. By this process, a relatively n...

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Main Authors: Xiaoyu Xia, Heng Cai, Shixiao Qin, Chen Xu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3492465?pdf=render
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spelling doaj-a6d36da97efe4dda8333763e870b25fc2020-11-25T02:16:00ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01711e4867310.1371/journal.pone.0048673Histone acetylase inhibitor curcumin impairs mouse spermiogenesis-an in vitro study.Xiaoyu XiaHeng CaiShixiao QinChen XuIn the previous study, we unraveled the unique "erasure strategy" during the mouse spermiogenesis. Chromatin associated proteins sequentially disassociated from the spermatid chromosome, which led to the termination of transcription in elongating spermatids. By this process, a relatively naïve paternal chromatin was generated, which might be essential for the zygotic development. We supposed the regulation of histone acetylation played an important role throughout this "erasure" process. In order to verify this hypothesis, we treated mouse spermatids in vitro by histone acetylase (HAT) inhibitor Curcumin. Our results showed an inhibiting effect of Curcumin on the growth of germ cell line in a dose-dependent manner. Accordingly, the apoptosis of primary haploid spermtids was increased by Curcumin treatment. As expected, the acetylated histone level was downregulated. Furthermore, we found the transcription in spermatids ceased in advance, the dynamics of chromatin associated factors was disturbed by Curcumin treatment. The regulation of histone acetylation should be one of the core reprogramming mechanisms during the spermiogenesis. The reproductive toxicity of Curcumin needs to be thoroughly investigated, which is crucial for its further clinical application.http://europepmc.org/articles/PMC3492465?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Xiaoyu Xia
Heng Cai
Shixiao Qin
Chen Xu
spellingShingle Xiaoyu Xia
Heng Cai
Shixiao Qin
Chen Xu
Histone acetylase inhibitor curcumin impairs mouse spermiogenesis-an in vitro study.
PLoS ONE
author_facet Xiaoyu Xia
Heng Cai
Shixiao Qin
Chen Xu
author_sort Xiaoyu Xia
title Histone acetylase inhibitor curcumin impairs mouse spermiogenesis-an in vitro study.
title_short Histone acetylase inhibitor curcumin impairs mouse spermiogenesis-an in vitro study.
title_full Histone acetylase inhibitor curcumin impairs mouse spermiogenesis-an in vitro study.
title_fullStr Histone acetylase inhibitor curcumin impairs mouse spermiogenesis-an in vitro study.
title_full_unstemmed Histone acetylase inhibitor curcumin impairs mouse spermiogenesis-an in vitro study.
title_sort histone acetylase inhibitor curcumin impairs mouse spermiogenesis-an in vitro study.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description In the previous study, we unraveled the unique "erasure strategy" during the mouse spermiogenesis. Chromatin associated proteins sequentially disassociated from the spermatid chromosome, which led to the termination of transcription in elongating spermatids. By this process, a relatively naïve paternal chromatin was generated, which might be essential for the zygotic development. We supposed the regulation of histone acetylation played an important role throughout this "erasure" process. In order to verify this hypothesis, we treated mouse spermatids in vitro by histone acetylase (HAT) inhibitor Curcumin. Our results showed an inhibiting effect of Curcumin on the growth of germ cell line in a dose-dependent manner. Accordingly, the apoptosis of primary haploid spermtids was increased by Curcumin treatment. As expected, the acetylated histone level was downregulated. Furthermore, we found the transcription in spermatids ceased in advance, the dynamics of chromatin associated factors was disturbed by Curcumin treatment. The regulation of histone acetylation should be one of the core reprogramming mechanisms during the spermiogenesis. The reproductive toxicity of Curcumin needs to be thoroughly investigated, which is crucial for its further clinical application.
url http://europepmc.org/articles/PMC3492465?pdf=render
work_keys_str_mv AT xiaoyuxia histoneacetylaseinhibitorcurcuminimpairsmousespermiogenesisaninvitrostudy
AT hengcai histoneacetylaseinhibitorcurcuminimpairsmousespermiogenesisaninvitrostudy
AT shixiaoqin histoneacetylaseinhibitorcurcuminimpairsmousespermiogenesisaninvitrostudy
AT chenxu histoneacetylaseinhibitorcurcuminimpairsmousespermiogenesisaninvitrostudy
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