Muscle injury causes long-term changes in stem-cell DNA methylation

Author:

Falick Michaeli Tal12,Sabag Ofra1,Fok Rimma1,Azria Batia1,Monin Jonathan3,Nevo Yuval4,Gielchinsky Yuval56,Berman Benjamin P.1ORCID,Cedar Howard1,Bergman Yehudit1ORCID

Affiliation:

1. Department of Developmental Biology and Cancer Research, Institute for Medical Research Israel-Canada, Hebrew University Medical School, Jerusalem 91120, Israel

2. Sharett Institute of Oncology, Hadassah-Hebrew University Medical Center, Jerusalem 91120, Israel

3. Hebrew University Medical School, Faculty of Medicine, The Hebrew University of Jerusalem, 91120, Israel

4. Info-CORE, Bioinformatics Unit of the Center of Research Excellence (I-CORE), Hebrew University and Hadassah Medical Center, Jerusalem 91120, Israel

5. Department of Obstetrics and Gynecology, Hadassah-Hebrew University Medical Center, Jerusalem 91120, Israel

6. Helen Schneider Hospital for Women, Rabin Medical Center, Petach Tikva 49100, Israel

Abstract

Injury to muscle brings about the activation of stem cells, which then generate new myocytes to replace damaged tissue. We demonstrate that this activation is accompanied by a dramatic change in the stem-cell methylation pattern that prepares them epigenetically for terminal myocyte differentiation. These de- and de novo methylation events occur at regulatory elements associated with genes involved in myogenesis and are necessary for activation and regeneration. Local injury of one muscle elicits an almost identical epigenetic change in satellite cells from other muscles in the body, in a process mediated by circulating factors. Furthermore, this same methylation state is also generated in muscle stem cells (MuSCs) of female animals following pregnancy, even in the absence of any injury. Unlike the activation-induced expression changes, which are transient, the induced methylation profile is stably maintained in resident MuSCs and thus represents a molecular memory of previous physiological events that is probably programmed to provide a mechanism for long-term adaptation.

Funder

Israel Science Foundation

Israel Cancer Research Fund

The Emanuel Rubin Chair in Medical Sciences

The Binational Science Foundation

The German-Israel Foundation

the Cooperation Program in Cancer Research of the Deutsches Krebsforschungszentrum (DKFZ) and Israel's Ministry of Science, Technology and Space

Rosetrees Trust

srael Science Foundation-physician scientist

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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