MeCP2-mediated epigenetic regulation in senescent endothelial progenitor cells

Abstract Background Cellular aging may be associated with epigenetics. Methyl-CpG-binding protein 2 (MeCP2) and sirtuin 1 (SIRT1) are two important epigenetic factors. Our former work demonstrated that MeCP2 expression increased and SIRT1 expression decreased in senescent endothelial progenitor cell...

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Main Authors: Chunli Wang, Fei Wang, Zhen Li, Qing Cao, Liya Huang, Shuyan Chen
Format: Article
Language:English
Published: BMC 2018-04-01
Series:Stem Cell Research & Therapy
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13287-018-0828-y
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spelling doaj-becd8b27f8754ee8881b7d6aede43e4d2020-11-25T02:22:11ZengBMCStem Cell Research & Therapy1757-65122018-04-01911710.1186/s13287-018-0828-yMeCP2-mediated epigenetic regulation in senescent endothelial progenitor cellsChunli Wang0Fei Wang1Zhen Li2Qing Cao3Liya Huang4Shuyan Chen5Department of Geriatrics, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of MedicineDepartment of Geriatrics, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of MedicineDepartment of Geriatrics, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of MedicineDepartment of Geriatrics, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of MedicineDepartment of Geriatrics, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of MedicineDepartment of Geriatrics, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of MedicineAbstract Background Cellular aging may be associated with epigenetics. Methyl-CpG-binding protein 2 (MeCP2) and sirtuin 1 (SIRT1) are two important epigenetic factors. Our former work demonstrated that MeCP2 expression increased and SIRT1 expression decreased in senescent endothelial progenitor cells (EPCs). This article aims to reveal the epigenetic regulation caused by MeCP2 in EPCs and discuss its mechanism. Methods Tube formation assay and cell apoptosis detection were used to evaluate the function of senescent EPCs induced by MeCP2 overexpression. Western blot analysis was used to testify the relative protein expression changed by MeCP2. Bisulfite sequencing methylation assay and chromatin immunoprecipitation assay were used to assess the degree of methylation and the relation of MeCP2 and SIRT1. Results MeCP2 reduced angiogenesis of senescent EPCs, promoted apoptosis, and caused senescent EPC dysfunction through SIRT1 promoter hypermethylation and histone modification. Conclusions MeCP2 mediated senescent EPC dysfunction through epigenetic regulation.http://link.springer.com/article/10.1186/s13287-018-0828-yEndothelial progenitor cellsSenescenceMeCP2SIRT1Epigenetic
collection DOAJ
language English
format Article
sources DOAJ
author Chunli Wang
Fei Wang
Zhen Li
Qing Cao
Liya Huang
Shuyan Chen
spellingShingle Chunli Wang
Fei Wang
Zhen Li
Qing Cao
Liya Huang
Shuyan Chen
MeCP2-mediated epigenetic regulation in senescent endothelial progenitor cells
Stem Cell Research & Therapy
Endothelial progenitor cells
Senescence
MeCP2
SIRT1
Epigenetic
author_facet Chunli Wang
Fei Wang
Zhen Li
Qing Cao
Liya Huang
Shuyan Chen
author_sort Chunli Wang
title MeCP2-mediated epigenetic regulation in senescent endothelial progenitor cells
title_short MeCP2-mediated epigenetic regulation in senescent endothelial progenitor cells
title_full MeCP2-mediated epigenetic regulation in senescent endothelial progenitor cells
title_fullStr MeCP2-mediated epigenetic regulation in senescent endothelial progenitor cells
title_full_unstemmed MeCP2-mediated epigenetic regulation in senescent endothelial progenitor cells
title_sort mecp2-mediated epigenetic regulation in senescent endothelial progenitor cells
publisher BMC
series Stem Cell Research & Therapy
issn 1757-6512
publishDate 2018-04-01
description Abstract Background Cellular aging may be associated with epigenetics. Methyl-CpG-binding protein 2 (MeCP2) and sirtuin 1 (SIRT1) are two important epigenetic factors. Our former work demonstrated that MeCP2 expression increased and SIRT1 expression decreased in senescent endothelial progenitor cells (EPCs). This article aims to reveal the epigenetic regulation caused by MeCP2 in EPCs and discuss its mechanism. Methods Tube formation assay and cell apoptosis detection were used to evaluate the function of senescent EPCs induced by MeCP2 overexpression. Western blot analysis was used to testify the relative protein expression changed by MeCP2. Bisulfite sequencing methylation assay and chromatin immunoprecipitation assay were used to assess the degree of methylation and the relation of MeCP2 and SIRT1. Results MeCP2 reduced angiogenesis of senescent EPCs, promoted apoptosis, and caused senescent EPC dysfunction through SIRT1 promoter hypermethylation and histone modification. Conclusions MeCP2 mediated senescent EPC dysfunction through epigenetic regulation.
topic Endothelial progenitor cells
Senescence
MeCP2
SIRT1
Epigenetic
url http://link.springer.com/article/10.1186/s13287-018-0828-y
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AT qingcao mecp2mediatedepigeneticregulationinsenescentendothelialprogenitorcells
AT liyahuang mecp2mediatedepigeneticregulationinsenescentendothelialprogenitorcells
AT shuyanchen mecp2mediatedepigeneticregulationinsenescentendothelialprogenitorcells
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