TY - JOUR
T1 - Nod1 acts as an intracellular receptor to stimulate chemokine production and neutrophil recruitment in vivo
AU - Masumoto, Junya
AU - Yang, Kangkang
AU - Varambally, Sooryanarayana
AU - Hasegawa, Mizuho
AU - Tomlins, Scott A.
AU - Qiu, Su
AU - Fujimoto, Yukari
AU - Kawasaki, Akiko
AU - Foster, Simon J.
AU - Horie, Yasuo
AU - Mak, Tak W.
AU - Núñez, Gabriel
AU - Chinnaiyan, Arul M.
AU - Fukase, Koichi
AU - Inohara, Naohiro
PY - 2006/1/23
Y1 - 2006/1/23
N2 - 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) α. Nod1 stimulation did not induce TNFα, interleukin 12, and interferon γ, 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. JEM
AB - 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) α. Nod1 stimulation did not induce TNFα, interleukin 12, and interferon γ, 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. JEM
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U2 - 10.1084/jem.20051229
DO - 10.1084/jem.20051229
M3 - Article
C2 - 16418393
AN - SCOPUS:31944437924
SN - 0022-1007
VL - 203
SP - 203
EP - 213
JO - Journal of Experimental Medicine
JF - Journal of Experimental Medicine
IS - 1
ER -