Nod1 acts as an intracellular receptor to stimulate chemokine production and neutrophil recruitment in vivo

被引:181
作者
Masumoto, J
Yang, K
Varambally, S
Hasegawa, M
Tomlins, SA
Qiu, S
Fujimoto, Y
Kawasaki, A
Foster, SJ
Horie, Y
Mak, TW
Núñez, G
Chinnaiyan, AM
Fukase, K
Inohara, N [1 ]
机构
[1] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Ctr Comprehens Canc, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Med, Dept Urol, Ann Arbor, MI 48109 USA
[4] Osaka Univ, Grad Sch Sci, Dept Chem, Toyonaka, Osaka 5600043, Japan
[5] Univ Sheffield, Dept Mol Biol & Biotechnol, Sheffield S10 2TN, S Yorkshire, England
[6] Univ Toronto, Ontario Canc Inst, Adv Med Discovery Inst, Toronto, ON M5G 2C1, Canada
[7] Univ Toronto, Dept Med Biophys & Immunol, Toronto, ON M5G 2C1, Canada
关键词
D O I
10.1084/jem.20051229
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Nod1 is a member of family of intracellular proteins that mediate host recognition of bacterial peptidoglycan. To characterize immune responses mediated by Nod1, synthetic ligand compounds possessing enhanced ability to stimulate Nod1 were developed to study the function of Nod1. Stimulation of epithelial cells with Nod1 stimulatory molecules induced chemokines and other proinflammatory molecules that are important for innate immune responses and recruitment of acute inflammatory cells. Administration of Nod1 ligands into mice induced chemokines and recruitment of acute inflammatory cells, an activity that was abolished in Nod1-null mice. Microarray analysis revealed that Nod1 stimulation induces a restricted number of genes in intestinal epithelial cells compared with that induced by tumor necrosis factor(TNF)alpha. Nod1 stimulation did not induce TNF alpha, interleukin 12, and interferon gamma, suggesting that the primary role of Nod1 is to induce the recruitment of immune cells. These results indicate that Nod1 functions as a pathogen recognition molecule to induce expression of molecules involved in the early stages of the innate immune response.
引用
收藏
页码:203 / 213
页数:11
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