Deconstructing Tick Saliva NON-PROTEIN MOLECULES WITH POTENT IMMUNOMODULATORY PROPERTIES


Autoria(s): OLIVEIRA, Carlo Jose F.; SA-NUNES, Anderson; FRANCISCHETTI, Ivo M. B.; CARREGARO, Vanessa; ANATRIELLO, Elen; SILVA, Joao S.; SANTOS, Isabel K. F. de Miranda; RIBEIRO, Jose M. C.; FERREIRA, Beatriz R.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2011

Resumo

Dendritic cells (DCs) are powerful initiators of innate and adaptive immune responses. Ticks are blood-sucking ectoparasite arthropods that suppress host immunity by secreting immunomodulatory molecules in their saliva. Here, compounds present in Rhipicephalus sanguineus tick saliva with immunomodulatory effects on DC differentiation, cytokine production, and costimulatory molecule expression were identified. R. sanguineus tick saliva inhibited IL-12p40 and TNF-alpha while potentiating IL-10 cytokine production by bone marrow-derived DCs stimulated by Toll-like receptor-2, -4, and -9 agonists. To identify the molecules responsible for these effects, we fractionated the saliva through microcon filtration and reversed-phase HPLC and tested each fraction for DC maturation. Fractions with proven effects were analyzed by micro-HPLC tandem mass spectrometry or competition ELISA. Thus, we identified for the first time in tick saliva the purine nucleoside adenosine (concentration of similar to 110pmol/mu l) as a potent anti-inflammatory salivary inhibitor of DC cytokine production. We also found prostaglandin E(2) (PGE(2) similar to 100 nM) with comparable effects in modulating cytokine production by DCs. Both Ado and PGE(2) inhibited cytokine production by inducing cAMP-PKA signaling in DCs. Additionally, both Ado and PGE(2) were able to inhibit expression of CD40 in mature DCs. Finally, flow cytometry analysis revealed that PGE(2), but not Ado, is the differentiation inhibitor of bone marrow-derived DCs. The presence of non-protein molecules adenosine and PGE(2) in tick saliva indicates an important evolutionary mechanism used by ticks to subvert host immune cells and allow them to successfully complete their blood meal and life cycle.

National Institutes of Health of the Division of Intramural Research, NIAID/NIH

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo[06/54985-4]

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo[07/00035-8]

CAPES Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Millennium Institute for Vaccine Development and Technology (Conselho Nacional de Desenvolvimento Cientifico e Tecnologico)[CNPq-420067/2005-1]

Identificador

JOURNAL OF BIOLOGICAL CHEMISTRY, v.286, n.13, p.10960-10969, 2011

0021-9258

http://producao.usp.br/handle/BDPI/20435

10.1074/jbc.M110.205047

http://dx.doi.org/10.1074/jbc.M110.205047

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 #DENDRITIC CELL-FUNCTION #TOLL-LIKE RECEPTOR-2 #LONE STAR TICK #RHIPICEPHALUS-SANGUINEUS #PROSTAGLANDIN E-2 #IXODES-SCAPULARIS #BOOPHILUS-MICROPLUS #AMBLYOMMA-AMERICANUM #MONOCYTE DIFFERENTIATION #BIOLOGICAL SIGNIFICANCE #Biochemistry & Molecular Biology
Tipo

article

original article

publishedVersion