Lepr‐Expressing PDLSCs Contribute to Periodontal Homeostasis and Respond to Mechanical Force by Piezo1

Author:

Zhang Danting1,Lin Weimin1,Jiang Shuang1,Deng Peng2,Liu Linfeng1,Wang Qian1,Sheng Rui1,Shu Hui Sophie3,Wang Lijun4,Zou Weiguo34,Zhou Bo O.35,Jing Junjun1,Ye Ling16,Yu Bo7,Zhang Shiwen18,Yuan Quan18ORCID

Affiliation:

1. State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases West China Hospital of Stomatology Sichuan University Chengdu 610041 China

2. Division of Oral and Systemic Health Sciences School of Dentistry University of California Los Angeles Los Angeles CA 90095 USA

3. State Key Laboratory of Cell Biology Shanghai Institute of Biochemistry and Cell Biology Center for Excellence in Molecular Cell Science Chinese Academy of Sciences University of Chinese Academy of Sciences Shanghai 200031 China

4. Institute of Microsurgery on Extremities Shanghai Jiao Tong University Affiliated Sixth People's Hospital Shanghai 200233 China

5. State Key Laboratory of Experimental Hematology Institute of Hematology & Blood Diseases Hospital Chinese Academy of Medical Sciences Tianjin 300020 China

6. Department of Endodontics West China Hospital of Stomatology Sichuan University Chengdu 610041 China

7. Division of Preventive and Restorative Sciences School of Dentistry University of California Los Angeles Los Angeles CA 90095 USA

8. Department of Oral Implantology West China Hospital of Stomatology Sichuan University Chengdu 610041 China

Abstract

AbstractPeriodontium supports teeth in a mechanically stimulated tissue environment, where heterogenous stem/progenitor populations contribute to periodontal homeostasis. In this study, Leptin receptor+ (Lepr+) cells are identified as a distinct periodontal ligament stem cell (PDLSC) population by single‐cell RNA sequencing and lineage tracing. These Lepr+ PDLSCs are located in the peri‐vascular niche, possessing multilineage potential and contributing to tissue repair in response to injury. Ablation of Lepr+ PDLSCs disrupts periodontal homeostasis. Hyper‐loading and unloading of occlusal forces modulate Lepr+ PDLSCs activation. Piezo1 is demonstrated that mediates the mechanosensing of Lepr+ PDLSCs by conditional Piezo1‐deficient mice. Meanwhile, Yoda1, a selective activator of Piezo1, significantly accelerates periodontal tissue growth via the induction of Lepr+ cells. In summary, Lepr marks a unique multipotent PDLSC population in vivo, to contribute toward periodontal homeostasis via Piezo1‐mediated mechanosensing.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

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