The broad effects of the functional IL-10 promoter-592 polymorphism: modulation of IL-10, TIMP-3, and OPG expression and their association with periodontal disease outcome


Autoria(s): CLAUDINO, Marcela; TROMBONE, Ana Paula F.; CARDOSO, Cristina R.; FERREIRA JR., Samuel B.; MARTINS JR., Walter; ASSIS, Gerson F.; SANTOS, Carlos F.; TREVILATTO, Paula C.; CAMPANELLI, Ana Paula; SILVA, Joao S.; GARLET, Gustavo P.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2008

Resumo

Periodontal diseases are infectious diseases, in which periodontopathogens trigger chronic inflammatory and immune responses that lead to tissue destruction. It occurs through the generation of metalloproteinases and the activation of bone resorption mechanisms. Anti-inflammatory cytokines such as IL-10 seem to attenuate periodontal tissue destruction through the induction of tissue inhibitors of metalloproteinases (TIMPs) and the inhibitor of osteoclastogenesis osteoprotegerin (OPG). A high individual variation in levels of IL-10 mRNA is verified in periodontitis patients, which is possibly determined by genetic polymorphisms. In this study, the IL-10 promoter -592C/A single nucleotide polymorphism ( SNP), which is associated with a decrease in IL-10 production, was analyzed by RFLP in 116 chronic periodontitis (CP) patients and 173 control (C) subjects, and the IL-10, TIMPs, and OPG mRNA expression levels in diseased gingival tissues were determined by real-time-PCR. The IL-10-592 SNP CA (P=0.0012/OR=2.4/CI:1.4-4.1), AA (P=0.0458/OR=2.3/CI:1.1-4.9), and CA+AA (P=0.0006/OR=2.4/CI: 1.4-3.4) genotypes and the allele A (P=0.0036/OR=1.7/CI:1.2-2.4) were found to be significantly more prevalent in the CP group when compared with control subjects. Both CA and AA genotypes were associated with lower levels of IL-10, TIMP-3, and OPG mRNA expression in diseased periodontal tissues and were also associated with disease severity as mean pocket depth. Taken together, the results presented here demonstrate that IL10-592 SNP is functional in CP, being associated with lower levels of IL-10 mRNA expression, which is supposed to consequently decrease the expression of the downstream genes TIMP-3 and OPG, and influence periodontal disease outcome. J. Leukoc. Biol. 84: 1565-1573; 2008.

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo

CNPq Conselho Nacional de Desenvolvimento Cientifico e Tecnologico

Identificador

JOURNAL OF LEUKOCYTE BIOLOGY, v.84, n.6, p.1565-1573, 2008

0741-5400

http://producao.usp.br/handle/BDPI/25875

10.1189/jlb.0308184

http://dx.doi.org/10.1189/jlb.0308184

Idioma(s)

eng

Publicador

FEDERATION AMER SOC EXP BIOL

Relação

Journal of Leukocyte Biology

Direitos

restrictedAccess

Copyright FEDERATION AMER SOC EXP BIOL

Palavras-Chave #interleukin-10 #genetic polymorphism #single nucleotide polymorphism #cytokine #immunoregulation #osteoprotegerin #periodontal disease #GINGIVAL CREVICULAR FLUID #INTERLEUKIN-10 GENE PROMOTER #SYSTEMIC-LUPUS-ERYTHEMATOSUS #PLAQUE-INDUCED GINGIVITIS #NECROSIS-FACTOR-ALPHA #ALVEOLAR BONE LOSS #AGGRESSIVE PERIODONTITIS #TISSUE INHIBITOR #ACTINOBACILLUS-ACTINOMYCETEMCOMITANS #MATRIX METALLOPROTEINASES #Cell Biology #Hematology #Immunology
Tipo

article

original article

publishedVersion