Murine Dendritic Cells Transcriptional Modulation upon Paracoccidioides brasiliensis Infection


Autoria(s): Tavares, Aldo H.; Derengowski, Lorena S.; Ferreira, Karen S.; Silva, Simoneide S.; Macedo, Claudia; Bocca, Anamelia L.; Passos, Geraldo A.; Almeida, Sandro Rogerio de; Silva-Pereira, Ildinete
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

14/10/2013

14/10/2013

2012

Resumo

Limited information is available regarding the modulation of genes involved in the innate host response to Paracoccidioides brasiliensis, the etiologic agent of paracoccidioidomycosis. Therefore, we sought to characterize, for the first time, the transcriptional profile of murine bone marrow-derived dendritic cells (DCs) at an early stage following their initial interaction with P. brasiliensis. DCs connect innate and adaptive immunity by recognizing invading pathogens and determining the type of effector T-cell that mediates an immune response. Gene expression profiles were analyzed using microarray and validated using real-time RT-PCR and protein secretion studies. A total of 299 genes were differentially expressed, many of which are involved in immunity, signal transduction, transcription and apoptosis. Genes encoding the cytokines IL-12 and TNF-alpha, along with the chemokines CCL22, CCL27 and CXCL10, were up-regulated, suggesting that P. brasiliensis induces a potent proinflammatory response in DCs. In contrast, pattern recognition receptor (PRR)-encoding genes, particularly those related to Toll-like receptors, were down-regulated or unchanged. This result prompted us to evaluate the expression profiles of dectin-1 and mannose receptor, two other important fungal PRRs that were not included in the microarray target cDNA sequences. Unlike the mannose receptor, the dectin-1 receptor gene was significantly induced, suggesting that this beta-glucan receptor participates in the recognition of P. brasiliensis. We also used a receptor inhibition assay to evaluate the roles of these receptors in coordinating the expression of several immune-related genes in DCs upon fungal exposure. Altogether, our results provide an initial characterization of early host responses to P. brasiliensis and a basis for better understanding the infectious process of this important neglected pathogen.

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico [CNPQ-proc. no. 476554/2007-1]

Fundacao de Amparo a Pesquisa do Distrito Federal

Fundacao de Amparo a Pesquisa do Distrito Federal

Identificador

PLOS NEGLECTED TROPICAL DISEASES, SAN FRANCISCO, v. 6, n. 1, pp. 1243-1248, JAN, 2012

1935-2727

http://www.producao.usp.br/handle/BDPI/34408

10.1371/journal.pntd.0001459

http://dx.doi.org/10.1371/journal.pntd.0001459

Idioma(s)

eng

Publicador

PUBLIC LIBRARY SCIENCE

SAN FRANCISCO

Relação

PLOS NEGLECTED TROPICAL DISEASES

Direitos

openAccess

Copyright PUBLIC LIBRARY SCIENCE

Palavras-Chave #NECROSIS-FACTOR-ALPHA #FUNGAL-INFECTIONS #CRYPTOCOCCUS-NEOFORMANS #ANTIFUNGAL IMMUNITY #IN-VITRO #INNATE #MICE #RESISTANCE #EXPRESSION #CHEMOKINE #INFECTIOUS DISEASES #PARASITOLOGY #TROPICAL MEDICINE
Tipo

article

original article

publishedVersion