Leukotrienes Produced in Allergic Lung Inflammation Activate Alveolar Macrophages


Autoria(s): SILVA, Reinaldo C.; LANDGRAF, Maristella A.; HIYANE, Meire I.; PACHECO-SILVA, Alvaro; CAMARA, Niels O.; LANDGRAF, Richardt G.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

It has been well-documented that leukotrienes (LTs) are released in allergic lung inflammation and that they participate in the physiopathology of asthma. A role for LTs in innate immunity has recently emerged: Cys-LTs were shown to enhance Fc gamma R-mediated phagocytosis by alveolar macrophages (AMs). Thus, using a rat model of asthma, we evaluated Fc gamma R-mediated phagocytosis and killing of Klebsiella pneumoniae by AMs. The effect of treatment with a cys-LT antagonist (montelukast) on macrophage function was also investigated. Male Wistar rats were immunized twice with OVA/alumen intraperitoneally and challenged with OVA aerosol. After 24 h, the animals were killed, and the AMs were obtained by bronchoalveolar lavage. Macrophages were cultured with IgG-opsonized red blood cells (50: 1) or IgG-opsonized K. pneumoniae (30: 1), and phagocytosis or killing was evaluated. Leukotriene C(4) and nitric oxide were quantified by the EIA and Griess methods, respectively. The results showed that AMs from sensitized and challenged rats presented a markedly increased phagocytic capacity via Fc gamma R (10X compared to controls) and enhanced killing of K. pneumoniae (4X higher than controls). The increased phagocytosis was inhibited 15X and killing 3X by treatment of the rats with montelukast, as compared to the non-treated group. cys-LT addition increased phagocytosis in control AMs but had no effect on macrophages from allergic lungs. Montelukast reduced nitric oxide (39%) and LTC(4) (73%). These results suggest that LTs produced during allergic lung inflammation potentiate the capacity of AMs to phagocytose and kill K. pneumonia via Fc gamma R. Copyright (C) 2010 S. Karger AG, Basel

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Complex Fluids INCT

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[07/07139-3]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[09/52119-6]

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)[10/01404-0]

Identificador

CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, v.26, n.3, p.319-326, 2010

1015-8987

http://producao.usp.br/handle/BDPI/28283

10.1159/000320555

http://dx.doi.org/10.1159/000320555

Idioma(s)

eng

Publicador

KARGER

Relação

Cellular Physiology and Biochemistry

Direitos

restrictedAccess

Copyright KARGER

Palavras-Chave #Alveolar macrophages #Leukotrienes #Asthma #Killing #Klebsiella pneumoniae #NITRIC-OXIDE PRODUCTION #PULMONARY TUBERCULOSIS #KLEBSIELLA-PNEUMONIAE #BACTERICIDAL ACTIVITY #PHAGOCYTOSIS #RECEPTOR #EXPRESSION #SYNTHASE #INJURY #MONTELUKAST #Cell Biology #Physiology
Tipo

article

original article

publishedVersion