Migration and differentiation of muscle stem cells are coupled by RhoA signalling during regeneration

Author:

Brondolin Mirco1ORCID,Herzog Dylan1,Sultan Sami1,Warburton Fiona2,Vigilante Alessandra3,Knight Robert D.1ORCID

Affiliation:

1. Centre for Craniofacial and Regenerative Biology, King's College London, Guy's Hospital, London, London SE1 9RT, UK

2. Oral Clinical Research Unit, King's College London, London, London SE1 9RT, UK

3. Centre for Stem Cells and Regenerative Medicine, London, London SE1 9RT, UK

Abstract

Skeletal muscle is highly regenerative and is mediated by a population of migratory adult muscle stem cells (muSCs). Effective muscle regeneration requires a spatio-temporally regulated response of the muSC population to generate sufficient muscle progenitor cells that then differentiate at the appropriate time. The relationship between muSC migration and cell fate is poorly understood and it is not clear how forces experienced by migrating cells affect cell behaviour. We have used zebrafish to understand the relationship between muSC cell adhesion, behaviour and fate in vivo . Imaging of pax7-expressing muSCs as they respond to focal injuries in trunk muscle reveals that they migrate by protrusive-based means. By carefully characterizing their behaviour in response to injury we find that they employ an adhesion-dependent mode of migration that is regulated by the RhoA kinase ROCK. Impaired ROCK activity results in reduced expression of cell cycle genes and increased differentiation in regenerating muscle. This correlates with changes to focal adhesion dynamics and migration, revealing that ROCK inhibition alters the interaction of muSCs to their local environment. We propose that muSC migration and differentiation are coupled processes that respond to changes in force from the environment mediated by RhoA signalling.

Funder

Royal Society

MRC

BBSRC

NC3Rs

Wellcome Trust

Publisher

The Royal Society

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology,General Neuroscience

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