| Literature DB >> 30338498 |
Janaina M Alves1,2, Antonio H Martins3,4, Claudiana Lameu4, Talita Glaser4, Nawal M Boukli5, Vinicius Bassaneze6, Rafael Dariolli6, Isis C Nascimento1,4, Poliana C M Martins4, Héllio D N de Souza4, José Eduardo Krieger6, Dulce E Casarini6, Vicencia M Sales7, João B Pesquero7, Henning Ulrich8.
Abstract
The bioactive peptide bradykinin obtained from cleavage of precursor kininogens activates the kinin-B2 receptor functioning in induction of inflammation and vasodilatation. In addition, bradykinin participates in kidney and cardiovascular development and neuronal and muscle differentiation. Here we show that kinin-B2 receptors are expressed throughout differentiation of murine C2C12 myoblasts into myotubes. An autocrine loop between receptor activation and bradykinin secretion is suggested, since bradykinin secretion is significantly reduced in the presence of the kinin-B2 receptor antagonist HOE-140 during differentiation. Expression of skeletal muscle markers and regenerative capacity were decreased after pharmacological inhibition or genetic ablation of the B2 receptor, while its antagonism increased the number of myoblasts in culture. In summary, the present work reveals to date no functions described for the B2 receptor in muscle regeneration due to the control of proliferation and differentiation of muscle precursor cells.Entities:
Keywords: HOE-140; Kinin-B2 receptor; Mouse myoblast differentiation; Muscle repair
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Year: 2019 PMID: 30338498 PMCID: PMC6613634 DOI: 10.1007/s12015-018-9850-9
Source DB: PubMed Journal: Stem Cell Rev Rep ISSN: 2629-3277 Impact factor: 5.739