Notch1 and Notch2 Coordinately Regulate Stem Cell Function in the Quiescent and Activated States of Muscle Satellite Cells

Author:

Fujimaki Shin123,Seko Daiki123,Kitajima Yasuo123,Yoshioka Kiyoshi123,Tsuchiya Yoshifumi123,Masuda Shinya12,Ono Yusuke124ORCID

Affiliation:

1. Musculoskeletal Molecular Biology Research Group, Basic and Translational Research Center for Hard Tissue Disease

2. Department of Stem Cell Biology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan

3. Japan Society for the Promotion of Science, Chiyoda-ku, Tokyo, Japan

4. Division of Regenerative Medicine Research, AMED, Chiyoda-ku, Tokyo, Japan

Abstract

Abstract Satellite cells, the muscle tissue stem cells, express three Notch receptors (Notch1–3). The function of Notch1 and Notch2 in satellite cells has to date not been fully evaluated. We investigated the role of Notch1 and Notch2 in myogenic progression in adult skeletal muscle using tamoxifen-inducible satellite cell-specific conditional knockout mice for Notch1 (N1-scKO), Notch2 (N2-scKO), and Notch1/Notch2 (scDKO). In the quiescent state, the number of satellite cells was slightly reduced in N2-scKO, but not significantly in N1-scKO, and almost completely depleted in scDKO mice. N1-scKO and N2-scKO mice both exhibited a defect in muscle regeneration induced by cardiotoxin injection, while muscle regeneration was severely compromised with marked fibrosis in scDKO mice. In the activated state, ablation of either Notch1 or Notch2 alone in satellite cells prevented population expansion and self-renewal but induced premature myogenesis. Therefore, our results indicate that Notch1 and Notch2 coordinately maintain the stem-cell pool in the quiescent state by preventing activation and regulate stem-cell-fate decision in the activated state, governing adult muscle regeneration.

Funder

Japan Science and Technology Agency

Japan Agency for Medical Research and Development

Grant-in-Aid for Scientific Research KAKENHI

Takeda Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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