TGF-beta and CD23 are involved in nitric oxide production by pulmonary macrophages activated by beta-glucan from Paracoccidioides brasiliensis


Autoria(s): QUEIROZ JR., Luiz de Padua; MATTOS JR., Marden Estevao; SILVA, Marcelo Fernandes da; SILVA, Celio Lopes
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

Resumo

Pulmonary macrophages (PM), which are CD11b/CD18(+) and CD23(+), may be involved in the onset of inflammatory events caused by Paracoccidioides brasiliensis in the lungs. In the present study, we measured the nitric oxide (NO) and interleukin in PM production after intratracheal (i.t.) inoculation of an enriched beta-glucan cell wall fraction from P. brasiliensis (Fraction F1). BALB/c and C57/BL6 (B6) mice were i.t. treated with Fraction F1, and their PM were restimulated in vitro with LPS and interferon-gamma up to 14 days after treatment. Macrophages BALB/c mice produced less NO than PM from B6 mice. The lower NO production was caused by higher production of TGF-beta by pulmonary macrophages of BALB/c and was abrogated by anti-TGF-beta MoAb in vitro and in vivo. Other interleukins such as IL-10, IL-4 and a combination of IL-1, TNF-alpha and IL-6 were not involved in NO production induced by Fraction F1. Expression of CD11b increases and expression of CD23 decreases on PM of BALB/c mice after in vivo treatment whereas PM of B6 mice do not show a variation of their phenotype. Moreover, the ability of pulmonary macrophages to induce lymphocyte proliferation was reduced in mixed cultures of CD11b(+) or CD23(+) macrophages but was restored when lymphocytes were cultivated in the presence of NO inhibitor (L-NMMA). Thus, the results presented herein indicate that in BALB/c but not in B6 mice TGF- is strongly induced by Fraction 1 in PM in vivo and suppresses NO production. Low NO production by PM is associated with a change in CD11b/CD23 expression and with a high lymphocyte proliferative response. Thus, CD11b(+)/CD23(+) PM modulate NO and TGF-beta production in the pulmonary microenvironment.

CNPq-Conselho Tecnologico de Pesquisa e Desenvolvimento

FAPESP-Fundacao de Amparo a Pesquisa do Estado de Sao Paulo

Programa de Apoio a Pesquisa da Universidade de Uberaba-PAPE- UNIUBE

Identificador

MEDICAL MICROBIOLOGY AND IMMUNOLOGY, v.199, n.1, p.61-69, 2010

0300-8584

http://producao.usp.br/handle/BDPI/23760

10.1007/s00430-009-0138-1

http://dx.doi.org/10.1007/s00430-009-0138-1

Idioma(s)

eng

Publicador

SPRINGER

Relação

Medical Microbiology and Immunology

Direitos

restrictedAccess

Copyright SPRINGER

Palavras-Chave #Experimental paracoccidioidomycosis #TGF-beta #CD23 #Nitric oxide #Inflammation #Bronchoalveolar lavage #Lung macrophages #GROWTH-FACTOR-BETA #REGULATORY T-CELLS #TOLL-LIKE RECEPTOR-2 #CYTOKINE PRODUCTION #CANDIDA-ALBICANS #ALVEOLAR MACROPHAGES #ADHESION MOLECULES #ENDOTHELIAL-CELLS #IMMUNE-RESPONSES #INTERFERON-GAMMA #Immunology #Microbiology
Tipo

article

original article

publishedVersion