Leukotrienes Target F-actin/Cofilin-1 to Enhance Alveolar Macrophage Anti-fungal Activity
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
---|---|
Data(s) |
20/10/2012
20/10/2012
2011
|
Resumo |
Candida albicans is the most common opportunistic fungal pathogen and causes local and systemic disease in immunocompromised patients. Alveolar macrophages (AMs) are pivotal for the clearance of C. albicans from the lung. Activated AMs secrete 5-lipoxygenase-derived leukotrienes (LTs), which in turn enhance phagocytosis and microbicidal activity against a diverse array of pathogens. Our aim was to investigate the role of LTB(4) and LTD(4) in AM antimicrobial functions against C. albicans and the signaling pathways involved. Pharmacologic and genetic inhibition of LT biosynthesis as well as receptor antagonism reduced phagocytosis of C. albicans when compared with untreated or WT controls. Conversely, exogenous LTs of both classes augmented base-line C. albicans phagocytosis by AMs. Although LTB(4) enhanced mainly mannose receptor-dependent fungal ingestion, LTD(4) enhanced mainly dectin-1 receptor-mediated phagocytosis. LT enhancement of yeast ingestion was dependent on protein kinase C-delta (PKC delta) and PI3K but not PKC alpha and MAPK activation. Both LTs reduced activation of cofilin-1, whereas they enhanced total cellular F-actin; however, LTB(4) accomplished this through the activation of LIM kinases (LIMKs) 1 and 2, whereas LTD(4) did so exclusively via LIMK-2. Finally, both exogenous LTB(4) and LTD(4) enhanced AM fungicidal activity in an NADPH oxidase-dependent manner. Our data identify LTB(4) and LTD(4) as key mediators of innate immunity against C. albicans, which act by both distinct and conserved signaling mechanisms to enhance multiple antimicrobial functions of AMs. U.S. National Institutes of Health (NIH) National Institutes of Health (NIH)[HL-058897] National Institutes of Health (NIH)[HL-103777-01] U.S. National Institutes of Health (NIH) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) CAPES Coordenação de Aperfeiçoamento de Pessoal de Nível Superior |
Identificador |
JOURNAL OF BIOLOGICAL CHEMISTRY, v.286, n.33, p.28902-28913, 2011 0021-9258 http://producao.usp.br/handle/BDPI/28265 10.1074/jbc.M111.235309 |
Idioma(s) |
eng |
Publicador |
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC |
Relação |
Journal of Biological Chemistry |
Direitos |
restrictedAccess Copyright AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC |
Palavras-Chave | #PROTEIN-KINASE CASCADE #CANDIDA-ALBICANS #NADPH OXIDASE #HOST-DEFENSE #5-LIPOXYGENASE METABOLISM #DEPENDENT PHAGOCYTOSIS #REGULATES PHAGOCYTOSIS #KLEBSIELLA-PNEUMONIAE #MURINE MACROPHAGES #BLOOD MONOCYTES #Biochemistry & Molecular Biology |
Tipo |
article original article publishedVersion |