Human endogenous RNAs: Implications for the immunomodulation of Toll-like receptor 3


Autoria(s): AMARANTE, Marla Karine; ODA, Julie Massayo Maeda; REICHE, Edna Maria Vissoci; MORIMOTO, Helena Kaminami; AOKI, Mateus Nobrega; WATANABE, Maria Angelica Ehara
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2011

Resumo

Toll-like receptors (TLRs), a family of mammalian receptors, are able to recognize nucleic acids. TLR3 recognizes double-stranded (ds)RNA, a product of the replication of certain viruses. Polyinosinic-polycytidylic acid, referred to as poly(I:C), an analog of viral dsRNA, interacts with TLR3 thereby eliciting immunoinflammatory responses characteristic of viral infection or down-regulating the expression of chemokine receptor CXCR4. It is known that dsRNA also directly activates interferon (IFN)-induced enzymes, such as the RNA-dependent protein kinase (PKR). In the present study, the mRNA expression of TLR3, CXCR4, IFN gamma and PKR was investigated in a culture of peripheral blood mononuclear cells (PBMCs) stimulated with poly(I:C) and endogenous RNA from human PBMCs. No cytotoxic effect on the cells or on the proliferation of CD3(+), CD4(+) and CD8(+) cells was observed. TLR3 expression in the PBMCs in the presence of poly(I:C) was up-regulated 9.5-fold, and TLR3 expression in the PBMCs treated with endogenous RNA was down-regulated 1.8-fold (p=0.002). The same trend was observed for IFN gamma where in the presence of poly(I:C) an 8.7-fold increase was noted and in the presence of endogenous RNA a 3.1-fold decrease was observed. In the culture activated with poly(1:C), mRNA expression of CXCR4 increased 8.0-fold and expression of PKR increased 33.0-fold. Expression of these genes decreased in the culture treated with endogenous RNA when compared to the culture without stimulus. Thus, high expression of mRNA for TLR3, IFN gamma, CXCR4 and PKR was observed in the presence of poly(I:C) and low expression was observed in the cells cultured with endogenous RNA. In conclusion, TLR3 may play major physiological roles that are not in the context of viral infection. It is possible that RNA released from cells could contain enough double-stranded structures to regulate cell activation. The involvement of endogenous RNA in endogenous gene expression and its implications in the regulation thereof, are still being studied, and will have significant implications in the future.

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)

Londrina State University Graduate Administration (PROPPG-UEL)

Londrina State University Graduate Administration (PROPPG-UEL)

Identificador

EXPERIMENTAL AND THERAPEUTIC MEDICINE, v.2, n.5, p.925-929, 2011

1792-0981

http://producao.usp.br/handle/BDPI/31481

10.3892/etm.2011.303

http://dx.doi.org/10.3892/etm.2011.303

Idioma(s)

eng

Publicador

SPANDIDOS PUBL LTD

Relação

Experimental and Therapeutic Medicine

Direitos

restrictedAccess

Copyright SPANDIDOS PUBL LTD

Palavras-Chave #Toll-like receptor 3 #CXCR4 #interferon-gamma #PKR #RNA #DOUBLE-STRANDED-RNA #INNATE IMMUNITY #MESSENGER-RNA #RECOGNITION #TLR3 #CELLS #ACTIVATION #APOPTOSIS #CANCER #PKR
Tipo

article

original article

publishedVersion