Please use this identifier to cite or link to this item: http://www.repositorio.ufop.br/handle/123456789/4495
Title: Angiotensin-(1-7) receptor Mas is an essential modulator of extracellular matrix protein expression in the heart.
Authors: Gava, Elisandra
Castro, Carlos Henrique de
Ferreira, Anderson José
Colleta, Heloísa
Melo, Marcos Barrouin
Alenina, Natalia
Bader, Michael
Oliveira, Laser Antônio Machado de
Santos, Robson Augusto Souza dos
Keywords: Angiotensin
Renin-angiotensin system
Fibrosis
Connective tissue
Extracellular matrix
Issue Date: 2012
Citation: GAVA, E. et al. Angiotensin-(1-7) receptor Mas is an essential modulator of extracellular matrix protein expression in the heart. Regulatory Peptides, v. 175, p. 30-42, 2012. Disponível em: <http://www.sciencedirect.com/science/article/pii/S016701151200002X>. Acesso em: 08 nov. 2014.
Abstract: In this study we investigated the effects of genetic deletion of the Angiotensin-(1-7) receptor Mas or the Angiotensin II receptor AT2 on the expression of specific extracellular matrix (ECM) proteins in atria, right ventricles and atrioventricular (AV) valves of neonatal and adult mice. Quantification of collagen types I, III and VI and fibronectin was performed using immunofluorescence-labeling and confocal microscopy. Picrosirius red staining was used for the histological assessment of the overall collagen distribution pattern. ECM proteins, metalloproteinases (MMP), ERK1/2 and p38 levels were quantified by western blot analysis. Gelatin zymography was used to evaluate the activity ofMMP-2 andMMP-9. We observed that the relative levels of collagen types I and III and fibronectin are significantly higher in both the right ventricle and AV valves of neonatal Mas−/− mouse hearts (e.g., collagen type I: 85.28±6.66 vs 43.50±4.41 arbitrary units in the right ventricles of Mas+/+ mice). Conversely, the level of collagen type VI was lower in the right ventricle and AV valves of Mas−/− mice. Adult Mas−/− mouse hearts presented similar patterns as observed in neonates. No significant differences in ECMprotein level were detected in atria. Likewise, no changes in ECM levels were observed in AT2 knockout mouse hearts. Although deletion of Mas induced a significant reduction in the level of the active form of MMP-2 in neonate hearts and a reduction of both MMP-2 and MMP-9 in adult Mas−/− mice, no significant differences were observed inMMP enzymatic activities when compared to controls. The levels of the active, phosphorylated forms of ERK1/2 and p38 were higher in hearts of both neonatal and adult Mas−/− mice. These observations suggest that Mas is involved in the selective expression of specific ECMproteins within both the ventricular myocardium and AV valves. The changes in the ECM profile may alter the connective tissue framework and contribute to the decreased cardiac performance observed in Mas−/− mice.
URI: http://www.repositorio.ufop.br/handle/123456789/4495
metadata.dc.identifier.doi: http://www.sciencedirect.com/science/article/pii/S016701151200002X
ISSN: 0167-0115
metadata.dc.rights.license: O periódico Regulatory Peptides concede permissão para depósito deste artigo no Repositório Institucional da UFOP. Número da licença: 3524850769887.
Appears in Collections:DECBI - Artigos publicados em periódicos

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