Kinin-B2 Receptor Activity in Skeletal Muscle Regeneration and Myoblast Differentiation

被引:11
作者
Alves, Janaina M. [1 ,2 ]
Martins, Antonio H. [3 ,4 ]
Lameu, Claudiana [4 ]
Glaser, Talita [4 ]
Boukli, Nawal M. [5 ]
Bassaneze, Vinicius [6 ]
Dariolli, Rafael [6 ]
Nascimento, Isis C. [1 ,4 ]
Martins, Poliana C. M. [4 ]
de Souza, Hellio D. N. [4 ]
Krieger, Jose Eduardo [6 ]
Casarini, Dulce E. [6 ]
Sales, Vicencia M. [7 ]
Pesquero, Joao B. [7 ]
Ulrich, Henning [4 ]
机构
[1] Univ Fed Sao Paulo, Dept Neurol Neurocirurgia, BR-04023900 Sao Paulo, Brazil
[2] Univ Cent Caribe, Dept Microbiol & Immunol, Bayamon, PR USA
[3] Univ Puerto Rico Med Sci Campus, Pharmacol & Toxicol Dept, Rio Piedras, PR USA
[4] Univ Sao Paulo, Inst Quim, Dept Bioquim, Av Prof Lineu Prestes 748, BR-05508000 Sao Paulo, SP, Brazil
[5] Univ Cent Caribe, Dept Microbiol & Immunol, Biomed Prote Facil, Bayamon, PR USA
[6] Univ Sao Paulo, Med Sch, Heart Inst InCor, Sao Paulo, Brazil
[7] Univ Fed Sao Paulo, Dept Biofis, BR-04023900 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
Mouse myoblast differentiation; Muscle repair; Kinin-B2; receptor; HOE-140; MYOGENIC DIFFERENTIATION; CELL-DIFFERENTIATION; MURINE MYOBLASTS; SATELLITE CELL; EXPRESSION; FUSION; GENES;
D O I
10.1007/s12015-018-9850-9
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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.
引用
收藏
页码:48 / 58
页数:11
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