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

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