Extraocular muscle stem cells exhibit distinct cellular properties associated with non-muscle molecular signatures

Author:

Girolamo Daniela Di12ORCID,Benavente-Diaz Maria123,Murolo Melania12ORCID,Grimaldi Alexandre123,Lopes Priscilla Thomas12,Evano Brendan12ORCID,Kuriki Mao12,Gioftsidi Stamatia456,Laville Vincent127,Tinevez Jean-Yves8,Letort Gaëlle9ORCID,Mella Sebastian7,Tajbakhsh Shahragim12ORCID,Comai Glenda12ORCID

Affiliation:

1. Institut Pasteur 1 Stem Cells and Development Unit, 25 rue du Dr Roux , , 75015 Paris , France

2. UMR CNRS 3738, Institut Pasteur 2 , Paris , France

3. Sorbonne Universités 3 , Complexité du Vivant, F-75005 Paris , France

4. Université Paris-Est 4 , 77420 Champs-sur- Marne , France

5. Freie Universität Berlin 5 , 14195 Berlin , Germany

6. Inserm, IMRB U955-E10 6 , 94000 Créteil , France

7. Institut Pasteur, Université Paris Cité, Bioinformatics and Biostatistics Hub 9 , F-75015 Paris , France

8. Institut Pasteur, Université Paris Cité 7 , Image Analysis Hub , 75015 Paris , France

9. Institut Pasteur, Université de Paris Cité, CNRS UMR 3738 8 Department of Developmental and Stem Cell Biology , , 25 rue du Dr Roux, 75015 Paris , France

Abstract

ABSTRACT Skeletal muscle stem cells (MuSCs) are recognised as functionally heterogeneous. Cranial MuSCs are reported to have greater proliferative and regenerative capacity when compared with those in the limb. A comprehensive understanding of the mechanisms underlying this functional heterogeneity is lacking. Here, we have used clonal analysis, live imaging and single cell transcriptomic analysis to identify crucial features that distinguish extraocular muscle (EOM) from limb muscle stem cell populations. A MyogeninntdTom reporter showed that the increased proliferation capacity of EOM MuSCs correlates with deferred differentiation and lower expression of the myogenic commitment gene Myod. Unexpectedly, EOM MuSCs activated in vitro expressed a large array of extracellular matrix components typical of mesenchymal non-muscle cells. Computational analysis underscored a distinct co-regulatory module, which is absent in limb MuSCs, as driver of these features. The EOM transcription factor network, with Foxc1 as key player, appears to be hardwired to EOM identity as it persists during growth, disease and in vitro after several passages. Our findings shed light on how high-performing MuSCs regulate myogenic commitment by remodelling their local environment and adopting properties not generally associated with myogenic cells.

Funder

Institut Pasteur

Agence Nationale de la Recherche

Association Française contre les Myopathies

Centre National de la Recherche Scientifique

Ligue Contre le Cancer

Uehara Memorial Foundation

Publisher

The Company of Biologists

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