The C allele of rs5743836 polymorphism in the human TLR9 promoter links IL-6 and TLR9 up-regulation and confers increased B-cell proliferation

In humans, allelic variants in Toll-like receptors (TLRs) associate with several pathologies. However, the underlying cellular and molecular mechanisms of this association remain largely unknown. Analysis of the human TLR9 promoter revealed that the C allele of the rs5743836 polymorphism generates s...

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Bibliographic Details
Main Author: Carvalho, Agostinho (author)
Other Authors: Osório, Nuno S. (author), Saraiva, Margarida (author), Cunha, Cristina (author), Almeida, A. J. (author), Coelho, Maria Teixeira (author), Ludovico, Paula (author), Pedrosa, Jorge (author), Pitzurra, Lucia (author), Aversa, Franco (author), Romani, Luigina (author), Castro, António G. (author), Rodrigues, Fernando José dos Santos (author)
Format: article
Language:eng
Published: 2011
Subjects:
Online Access:http://hdl.handle.net/1822/18618
Country:Portugal
Oai:oai:repositorium.sdum.uminho.pt:1822/18618
Description
Summary:In humans, allelic variants in Toll-like receptors (TLRs) associate with several pathologies. However, the underlying cellular and molecular mechanisms of this association remain largely unknown. Analysis of the human TLR9 promoter revealed that the C allele of the rs5743836 polymorphism generates several regulatory sites, including an IL-6-responding element. Here, we show that, in mononuclear cells carrying the TC genotype of rs5743836, IL-6 up-regulates TLR9 expression, leading to exacerbated cellular responses to CpG, including IL-6 production and B-cell proliferation. Our study uncovers a role for the rs5743836 polymorphism in B-cell biology with implications on TLR9-mediated diseases and on the therapeutic usage of TLR9 agonists/antagonists.