Nitric oxide participation in granulomatous response induced by Paracoccidioides brasiliensis infection in mice


Autoria(s): NISHIKAKU, Angela Satie; MOLINA, Raphael Fagnani Sanchez; RIBEIRO, Luciana Cristina; SCAVONE, Renata; ALBE, Bernardo Paulo; CUNHA, Claudia Silva; BURGER, Eva
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

The role of nitric oxide (NO) in granulomas of Paracoccidioides brasiliensis-infected inducible NO synthase-deficient C57BL/6 mice (iNOS KO) and their wild-type counterparts and its association with osteopontin (OPN) and matrix metalloproteinases (MMPs) was studied. At 15 days after infection (DAI), iNOS KO mice showed compact and necrotic granulomas with OPN+ macrophages and multinucleated giant cells, whereas wild-type mice developed loose granulomas with many fungi and OPN+ cells distributed throughout the tissue. In addition, high OPN levels and fungal load were observed in iNOS KO mice. Both experimental groups had MMP-9 activity. At 120 DAI, iNOS KO had smaller granulomas with OPN+ cells, lower OPN levels, lower fungal load and decreased MMP-9 activity compared with wild-type mice. These findings suggest that NO has an important role in granuloma modulation, by controlling OPN and MMP production, as well as by inducing loose granulomas formation and fungal dissemination, resulting, at later phases, in progression of paracoccidioidomycosis.

Identificador

MEDICAL MICROBIOLOGY AND IMMUNOLOGY, v.198, n.2, p.123-135, 2009

0300-8584

http://producao.usp.br/handle/BDPI/28305

10.1007/s00430-009-0113-x

http://dx.doi.org/10.1007/s00430-009-0113-x

Idioma(s)

eng

Publicador

SPRINGER

Relação

Medical Microbiology and Immunology

Direitos

restrictedAccess

Copyright SPRINGER

Palavras-Chave #Experimental paracoccidioidomycosis #Inducible nitric oxide synthase #Granulomas #Osteopontin #Matrix metalloproteinases #MATRIX METALLOPROTEINASES #INBRED MICE #MURINE MACROPHAGES #CELL BEHAVIOR #EUTHYMIC MICE #L-ARGININE #IN-VIVO #OSTEOPONTIN #RESISTANCE #CYTOKINES #Immunology #Microbiology
Tipo

article

original article

publishedVersion