Inhibitory SMAD6 interferes with BMP dependent generation of muscle progenitor cells and perturbs proximodistal pattern of murine limb muscles

Author:

Asfour Hasan1ORCID,Hirsinger Estelle2ORCID,Rouco Raquel3ORCID,Zarrouki Faouzi1ORCID,Hayashi Shinichiro4ORCID,Swist Sandra5ORCID,Braun Thomas5ORCID,Patel Ketan6ORCID,Relaix Frédéric7ORCID,Andrey Guillaume3ORCID,Stricker Sigmar8ORCID,Duprez Delphine2ORCID,Stantzou Amalia1ORCID,Amthor Helge19ORCID

Affiliation:

1. 1 Université Paris-Saclay, UVSQ, Inserm, END-ICAP, 78000 Versailles, France

2. 2 Sorbonne Université, Institut Biologie Paris Seine, CNRS UMR7622, Developmental Biology Laboratory, Inserm U1156, 75005 Paris, France

3. 3 University of Geneva, Faculty of Medicine, Department of Genetic Medicine and Development, 1211 Geneva 4, Switzerland

4. 4 National Center of Neurology and Psychiatry (NCNP), National Institute of Neuroscience, Department of Neuromuscular Research, Tokyo 187-8502, Japan

5. 5 Max-Planck-Institute for Heart and Lung Research, Department of Cardiac Development and Remodeling, 61231 Bad Nauheim, Germany

6. 6 University of Reading, School of Biological Sciences, Reading RG6 6AH, UK

7. 7 Université Paris Est Créteil, INSERM, EnvA, EFS, AP-HP, IMRB, 94010 Créteil, France

8. 8 Freie Universität Berlin, Institute for Chemistry and Biochemistry, 14195 Berlin, Germany

9. 9 AP-HP, Hôpital Raymond Poincaré, Service de Pédiatrie, 92380 Garches, France

Abstract

The mechanism of pattern formation during limb muscle development remains poorly understood. The canonical view holds that naïve limb muscle progenitor cells (MPCs) invade a pre-established pattern of muscle connective tissue, thereby forming individual muscles. Here we show that early murine embryonic limb MPCs highly accumulate pSMAD1/5/9, demonstrating active signaling of bone morphogenetic proteins (BMP) in these cells. Overexpression of inhibitory SMAD6 in limb MPCs abrogated BMP signaling, impaired their migration and proliferation, and accelerated myogenic lineage progression. Fewer primary myofibers developed, causing an aberrant proximodistal muscle pattern. Patterning was not disturbed when SMAD6 was overexpressed in differentiated muscle, implying that the proximodistal muscle pattern depends on BMP-mediated expansion of MPCs prior to their differentiation. We show that limb MPCs differentially express Hox genes, and Hox-expressing MPCs displayed active BMP signaling. SMAD6 overexpression caused loss of HOXA11 in early limb MPCs. In conclusion, our data show that BMP signaling controls expansion of embryonic limb MPC as a prerequisite for establishing the proximodistal muscle pattern, a process that involves expression of Hox genes.

Funder

Association Francaise contre les Myopathies

Agence Nationale de la Recherche

Deutsch-Franzsische Hochschule

Schweizerischer Nationalfonds zur Furderung der Wissenschaftlichen Forschung

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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