Cotinine inhibits the pro-inflammatory response initiated by multiple cell surface Toll-like receptors in monocytic THP cells.
Cotinine inhibits the pro-inflammatory response initiated by multiple cell surface Toll-like receptors in monocytic THP cells.
复制标题
DOI:
10.1186/1617-9625-10-18
复制
发表时间:
2012-11-23
影响因子:
3.7
通讯作者:
Scott DA
中科院分区:
文献类型:
--
作者:
Bagaitkar J;Zeller I;Renaud DE;Scott DA
The primary, stable metabolite of nicotine [(S)-3-(1-methyl-2-pyrrolidinyl) pyridine] in humans is cotinine [(S)-1-methyl-5-(3-pyridinyl)-2-pyrrolidinone]. We have previously shown that cotinine exposure induces convergence and amplification of the GSK3β-dependent PI3 kinase and cholinergic anti-inflammatory systems. The consequence is reduced pro-inflammatory cytokine secretion by human monocytes responding to bacteria or LPS, a TLR4 agonist. Here we show that cotinine-induced inflammatory suppression may not be restricted to individual Toll-like receptors (TLRs). Indeed, in monocytic cells, cotinine suppresses the cytokine production that is normally resultant upon agonist-specific engagement of all of the major surface exposed TLRs (TLR 2/1; 2/6; 4 and 5), although the degree of suppression varies by TLR. These results provide further mechanistic insight into the increased susceptibility to multiple bacterial infections known to occur in smokers. They also establish THP-1 cells as a potentially suitable model with which to study the influence of tobacco components and metabolites on TLR-initiated inflammatory events.
登录
查看更多内容
DOI:
10.1016/j.bbamcr.2007.12.003
发表时间:
2008-03-01
影响因子:
5.1
作者:
Rehani, Kunal;Scott, David A.;Martin, Michael
通讯作者:
Martin, Michael
影响因子:
5.2
作者:
Oke SL;Tracey KJ
通讯作者:
Tracey KJ
DOI:
10.1161/atvbaha.112.255208
发表时间:
2012-12-01
影响因子:
8.7
作者:
Bojic, Lazar A.;Sawyez, Cynthia G.;Huff, Murray W.
通讯作者:
Huff, Murray W.
DOI:
10.1084/jem.20052362
发表时间:
2006-07-10
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Huston JM;Ochani M;Rosas-Ballina M;Liao H;Ochani K;Pavlov VA;Gallowitsch-Puerta M;Ashok M;Czura CJ;Foxwell B;Tracey KJ;Ulloa L
通讯作者:
Ulloa L
影响因子:
64.8
作者:
Borovikova, LV;Ivanova, S;Tracey, KJ
通讯作者:
Tracey, KJ