Leukotrienes Target F-actin/Cofilin-1 to Enhance Alveolar Macrophage Anti-fungal Activity


Autoria(s): MORATO-MARQUES, Mariana; CAMPOS, Marina R.; KANE, Steve; RANGEL, Ana P.; LEWIS, Casey; BALLINGER, Megan N.; KIM, Sang-Hoon; PETERS-GOLDEN, Marc; JANCAR, Sonia; SEREZANI, Carlos H.
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

http://dx.doi.org/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