Toll-like receptor 2-dependent bacterial sensing does not occur via peptidoglycan recognition

被引:385
作者
Travassos, LH
Girardin, SE
Philpott, DJ
Blanot, D
Nahori, MA
Werts, C
Boneca, IG
机构
[1] Inst Pasteur, Unite Pathogenie Bacterienne Muqueuses, F-75724 Paris 15, France
[2] Inst Pasteur, Grp Immun Innee & Signalisat, F-75724 Paris 15, France
[3] Inst Pasteur, Unite Pathogenie Microbienne Mol, F-75724 Paris 15, France
[4] Inst Pasteur, Unite Postulante Cytokines & Inflammat, F-75724 Paris 15, France
[5] Univ Fed Rio de Janeiro, Ctr Ciencias Saude, Inst Microbiol Paulo de Goes, BR-21941590 Rio De Janeiro, Brazil
[6] Univ Paris 11, Inst Biochim & Biophys Mol & Cellulaire, CNRS, UMR 8619, F-91405 Orsay, France
关键词
peptidoglycan; LTA; Nod2; cytokine; macrophage; TLR;
D O I
10.1038/sj.embor.7400248
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Toll-like receptor 2 (TLR2) has been shown to recognize several classes of pathogen-associated molecular patterns including peptidoglycan (PG). However, studies linking PG with TLR2 recognition have relied mainly on the use of commercial Staphylococcus aureus PG and have not addressed TLR2 recognition of other PG types. Using highly purified PGs from eight bacteria (Escherichia coli, Pseudomonas aeruginosa, Yersinia pseudotuberculosis, Helicobacter pylori, Bacillus subtilis, Listeria monocytogenes, Streptococcus pneumoniae and S. aureus), we show that these PGs are not sensed through TLR2, TLR2/1 or TLR2/6. PG sensing is lost after removal of lipoproteins or lipoteichoic acids (LTAs) from Gram-negative and Gram-positive cell walls, respectively. Accordingly, purified LTAs are sensed synergistically through TLR2/1. Finally, we show that elicited peritoneal murine macrophages do not produce tumour necrosis factor-alpha or interleukin-6 in response to purified PGs, suggesting that PG detection is more likely to occur intracellularly (through Nod1/Nod2) rather than from the extracellular compartment.
引用
收藏
页码:1000 / 1006
页数:7
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