GPR43 regulates sodium butyrate-induced angiogenesis and matrix remodeling

Author:

Castro Pollyana Ribeiro1ORCID,Bittencourt Lucas Felipe Fernandes1ORCID,Larochelle Sébastien2,Andrade Silvia Passos1,Mackay Charles Reay3,Slevin Mark4,Moulin Véronique J.25ORCID,Barcelos Lucíola Silva1

Affiliation:

1. Department of Physiology and Biophysics, Institute of Biological Sciences, Federal University of Minas Gerais (UFMG), Belo Horizonte, Brazil

2. Centre de Recherche en Organogénèse Expérimentale de l'Université Laval/LOEX, Centre de recherche du CHU de Québec-Université Laval, Quebec, Canada

3. Department of Immunology, Monash University, Clayton, Victoria, Australia

4. School of Healthcare Science, GMBC, Manchester Metropolitan University, Manchester, United Kingdom

5. Department of Surgery, Faculty of Medicine, Université Laval, Quebec, Canada

Abstract

Our data show the contribution of the metabolite-sensing receptor GPR43 in the effects of low dose of sodium butyrate (NaBu) on stimulating angiogenesis and extracellular matrix remodeling in a model of granulation tissue formation in mice. We also show that human dermal fibroblasts, myofibroblasts, and endothelial cells express the receptor GPR43. These data provide important insights for the use of NaBu in local therapeutic approaches applicable to tissue repair in sites other than the intestine.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Conselho Nacional de Pesquisa

Fundação de Amparo à Pesquisa de Minas Gerais

National Institute of Science and Technology (INCT-NanoBiofar) – Brazil

Publisher

American Physiological Society

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

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