期刊
CARDIOVASCULAR RESEARCH
卷 99, 期 2, 页码 364-373出版社
OXFORD UNIV PRESS
DOI: 10.1093/cvr/cvt033
关键词
Atherosclerosis; TRAM; TRIF; TLR3; Vascular inflammation
资金
- Swedish Research Council [6816, 8703]
- Swedish Heart-Lung Foundation
- European Commission
- Foundation for Strategic Research
- Vinnova Foundation, Stockholm County Council
- Konung Gustaf V:s 80-years fond
- Loo and Osterman's foundation
- O. E. and Edla Johansson's Foundation
- Magnus Bergvall's Foundation
- Prof. Nanna Svartz Foundation
- Gun and Bertil Stohne's Foundation
- KI Foundations for Geriatric Research
Aims Members of the Toll-like receptor (TLR) family initiate innate immune responses and were recently shown to play a role in atherosclerosis. However, the mechanisms that link TLR ligation to vascular inflammation and atherogenesis remain unclear. To identify which signalling pathways downstream of TLRs in immune cells are pro-atherogenic, we analysed the role of the TLR-specific adaptors MyD88 adaptor-like (MAL), TRIF-related adaptor molecule (TRAM), and TIR-domain-containing adaptor-inducing interferon-beta (TRIF) in atherosclerosis. Methods and results Using a bone-marrow transplantation strategy into low-density lipoprotein receptor-deficient (Ldlr(-/-)) mice, we could specifically study the absence of the TLR adaptors in immune cells. We showed that haematopoietic deficiency of TRAM and TRIF, but not MAL, reduces atherosclerosis without affecting cholesterol metabolism. This was mediated by decreased aortic inflammation, indicated by lower aortic levels of pro-inflammatory mediators, and reduced influx of macrophages and T cells. Furthermore, by studying Tlr3(-/-) chimeric Ldlr(-/-) mice, we found that deleting TLR3 in immune cells significantly reduced both aortic inflammation and atherosclerotic burden. Conclusions By studying hypercholesterolaemic mice with defects in TLR-signalling adaptors, we demonstrated that deleting either TRAM or TRIF in immune cells is sufficient to attenuate vessel inflammation and protect against atherosclerosis. In addition, these adaptors elicit partly different sets of inflammatory mediators and can independently inhibit the disease process. Furthermore, we identify TLR3 as a pro-atherogenic receptor in haematopoietic immune cells. The identification of these pro-atherogenic pathways downstream of TLR3 and TLR4 contributes to a better understanding of TLRs and their signalling pathways in the pathogenesis of atherosclerosis.
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