Epigenetic Regulation of Methylation in Determining the Fate of Dental Mesenchymal Stem Cells

Author:

Zhang Hui1ORCID,Fu Hong1ORCID,Fang Hongzhi2ORCID,Deng Qing1ORCID,Huang Hao3,Hou Dingyu3,Wang Miaomiao4,Yao Quanzhou1,Si Qiqi5ORCID,Chen Rui1ORCID,Li Linke1ORCID,Weng Jie3ORCID,Guo Tailin1ORCID,Wang Mengyuan26ORCID

Affiliation:

1. College of Medicine, Southwest Jiaotong University, Chengdu, Sichuan, 610031, China

2. Department of stomatology, The Third People’s Hospital of Chengdu, The Affiliated Hospital of Southwest Jiaotong University, Chengdu, Sichuan, 610000, China

3. College of Materials Science and Engineering, Southwest Jiaotong University, Chengdu, Sichuan, 610031, China

4. College of Analysis and Testing Center, Southwest Jiaotong University, Chengdu, Sichuan, 610031, China

5. College of Life Science, Southwest Jiaotong University, Chengdu, Sichuan, 610031, China

6. The Center of Obesity and Metabolic Diseases, Department of General Surgery, The Third People’s Hospital of Chengdu & The Affiliated Hospital of Southwest Jiaotong University, No. 19 Yangshi Road, Chengdu, Sichuan, 610031, China

Abstract

Dental mesenchymal stem cells (DMSCs) are crucial in tooth development and periodontal health, and their multipotential differentiation and self-renewal ability play a critical role in tissue engineering and regenerative medicine. Methylation modifications could promote the appropriate biological behavior by postsynthetic modification of DNA or protein and make the organism adapt to developmental and environmental prompts by regulating gene expression without changing the DNA sequence. Methylation modifications involved in DMSC fate include DNA methylation, RNA methylation, and histone modifications, which have been proven to exert a significant effect on the regulation of the fate of DMSCs, such as proliferation, self-renewal, and differentiation potential. Understanding the regulation of methylation modifications on the behavior and the immunoinflammatory responses involved in DMSCs contributes to further study of the mechanism of methylation on tissue regeneration and inflammation. In this review, we briefly summarize the key functions of histone methylation, RNA methylation, and DNA methylation in the differentiation potential and self-renewal of DMSCs as well as the opportunities and challenges for their application in tissue regeneration and disease therapy.

Funder

Fundamental Research Funds for Central University

Publisher

Hindawi Limited

Subject

Cell Biology,Molecular Biology

Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3