BAY 41-2272, a soluble guanylate cyclase agonist, activates human mononuclear phagocytes


Autoria(s): Soeiro-Pereira, P. V.; Falcai, A.; Kubo, C. A.; Oliveira-Junior, E. B.; Marques, O. C.; Antunes, E.; Condino-Neto, A.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

12/09/2013

12/09/2013

2012

Resumo

BACKGROUND AND PURPOSE Phagocyte function is critical for host defense against infections. Defects in phagocytic function lead to several primary immunodeficiencies characterized by early onset of recurrent and severe infections. In this work, we further investigated the effects of BAY 41-2272, a soluble guanylate cyclase (sGC) agonist, on the activation of human peripheral blood monocytes (PBM) and THP-1 cells. EXPERIMENTAL APPROACH THP-1 cells and PBM viability was evaluated by methylthiazoletetrazolium assay; reactive oxygen species production by lucigenin chemiluminescence; gene and protein expression of NAPDH oxidase components by qRT-PCR and Western blot analysis, respectively; phagocytosis and microbicidal activity by co-incubation, respectively, with zymosan and Escherichia coli; and cytokine release by elisa. KEY RESULTS BAY 41-2272, compared with the untreated group, increased spreading of monocytes by at least 35%, superoxide production by at least 50%, and gp91PHOX and p67PHOX gene expression 20 to 40 times, in both PBM and THP-1 cells. BAY 41-2272 also augmented phagocytosis of zymosan particles threefold compared with control, doubled microbicidal activity against E. coli and enhanced the release of TNF-a and IL-12p70 by both PBM and THP-1 cells. Finally, by inhibiting sGC with ODQ, we showed that BAY 41-2272-induced superoxide production and phagocytosis is not dependent exclusively on sGC activation. CONCLUSIONS AND IMPLICATIONS In addition to its ability to induce vasorelaxation and its potential application for therapy of vascular diseases, BAY 41-2272 was shown to activate human mononuclear phagocytes. Hence, it is a novel pro-inflammatory drug that may be useful for controlling infections in the immunocompromised host.

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo [06/51004-2, 06/52483-1]

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico [470978/2008-2]

Identificador

BRITISH JOURNAL OF PHARMACOLOGY, HOBOKEN, v. 166, n. 5, pp. 1617-1630, JUL, 2012

0007-1188

http://www.producao.usp.br/handle/BDPI/33298

10.1111/j.1476-5381.2011.01764.x

http://dx.doi.org/10.1111/j.1476-5381.2011.01764.x

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

HOBOKEN

Relação

BRITISH JOURNAL OF PHARMACOLOGY

Direitos

restrictedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #BAY 41-2272 #CGMP #NADPH OXIDASE #GP91PHOX #P67PHOX #MICROBICIDAL ACTIVITY #CHRONIC GRANULOMATOUS-DISEASE #CHAIN GENE-EXPRESSION #CYTOCHROME-B HEAVY #NITRIC-OXIDE #INTERFERON-GAMMA #PROTEIN-KINASE #HUMAN NEUTROPHILS #NADPH OXIDASE #BINDING PROTEIN #RAT NEUTROPHILS #FAGÓCITOS MONONUCLEARES #FAGOCITOSE #PHARMACOLOGY & PHARMACY
Tipo

article

original article

publishedVersion