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Inhibitory SMAD6 interferes with BMP-dependent generation of muscle progenitor cells and perturbs proximodistal pattern of murine limb muscles.
Asfour, Hasan; Hirsinger, Estelle; Rouco, Raquel; Zarrouki, Faouzi; Hayashi, Shinichiro; Swist, Sandra; Braun, Thomas; Patel, Ketan; Relaix, Frédéric; Andrey, Guillaume; Stricker, Sigmar; Duprez, Delphine; Stantzou, Amalia; Amthor, Helge.
Affiliation
  • Asfour H; Université Paris-Saclay, UVSQ, Inserm, END-ICAP, 78000 Versailles, France.
  • Hirsinger E; Sorbonne Université, Institut Biologie Paris Seine, CNRS UMR7622, Developmental Biology Laboratory, Inserm U1156, 75005 Paris, France.
  • Rouco R; Faculty of Medicine, Department of Genetic Medicine and Development, University of Geneva, 1211 Geneva 4, Switzerland.
  • Zarrouki F; Université Paris-Saclay, UVSQ, Inserm, END-ICAP, 78000 Versailles, France.
  • Hayashi S; Department of Neuromuscular Research, National Center of Neurology and Psychiatry (NCNP), National Institute of Neuroscience, Tokyo 187-8502, Japan.
  • Swist S; Department of Cardiac Development and Remodeling, Max-Planck-Institute for Heart and Lung Research, 61231 Bad Nauheim, Germany.
  • Braun T; Department of Cardiac Development and Remodeling, Max-Planck-Institute for Heart and Lung Research, 61231 Bad Nauheim, Germany.
  • Patel K; School of Biological Sciences, University of Reading, Reading RG6 6AH, UK.
  • Relaix F; Université Paris Est Créteil, INSERM, EnvA, EFS, AP-HP, IMRB, 94010 Créteil, France.
  • Andrey G; Faculty of Medicine, Department of Genetic Medicine and Development, University of Geneva, 1211 Geneva 4, Switzerland.
  • Stricker S; Institute for Chemistry and Biochemistry, Freie Universität Berlin,14195 Berlin, Germany.
  • Duprez D; Sorbonne Université, Institut Biologie Paris Seine, CNRS UMR7622, Developmental Biology Laboratory, Inserm U1156, 75005 Paris, France.
  • Stantzou A; Université Paris-Saclay, UVSQ, Inserm, END-ICAP, 78000 Versailles, France.
  • Amthor H; Université Paris-Saclay, UVSQ, Inserm, END-ICAP, 78000 Versailles, France.
Development ; 150(11)2023 06 01.
Article in En | MEDLINE | ID: mdl-37272529
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 human SMAD6 (huSMAD6) 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 huSMAD6 was overexpressed in differentiated muscle, implying that the proximodistal muscle pattern depends on BMP-mediated expansion of MPCs before their differentiation. We show that limb MPCs differentially express Hox genes, and Hox-expressing MPCs displayed active BMP signaling. huSMAD6 overexpression caused loss of HOXA11 in early limb MPCs. In conclusion, our data show that BMP signaling controls expansion of embryonic limb MPCs as a prerequisite for establishing the proximodistal muscle pattern, a process that involves expression of Hox genes.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Muscle, Skeletal / Bone Morphogenetic Proteins Limits: Animals / Humans Language: En Journal: Development Journal subject: BIOLOGIA / EMBRIOLOGIA Year: 2023 Document type: Article Affiliation country: Francia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Muscle, Skeletal / Bone Morphogenetic Proteins Limits: Animals / Humans Language: En Journal: Development Journal subject: BIOLOGIA / EMBRIOLOGIA Year: 2023 Document type: Article Affiliation country: Francia