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J. Exp. Med., Volume 189, Number 4, February 15, 1999 615-625

Endotoxin-tolerant Mice Have Mutations in Toll-like Receptor 4 (Tlr4)

By Salman T. Qureshi,*parallel Line Larivière,parallel Gary Leveque,parallel Sophie Clermont,parallel Karen J. Moore, Philippe Gros,Dagger parallel and Danielle Malo*§parallel

From the * Department of Medicine, Dagger  Department of Biochemistry, and § Department of Human Genetics, McGill University, Montreal, Quebec, Canada H3G 1A4; the parallel  Centre for the Study of Host Resistance, Montreal General Hospital, Montreal, Quebec, Canada H3G 1A4; and  Millennium Pharmaceuticals, Inc., Cambridge, Massachusetts 02139

Bacterial lipopolysaccharide (LPS) provokes a vigorous, generalized proinflammatory state in the infected host. Genetic regulation of this response has been localized to the Lps locus on mouse chromosome 4, through study of the C3H/HeJ and C57BL/10ScCr inbred strains. Both C3H/HeJ and C57BL/10ScCr mice are homozygous for a mutant Lps allele (Lpsd/d) that confers hyporesponsiveness to LPS challenge, and therefore exhibit natural tolerance to its lethal effects. Genetic and physical mapping of 1,345 backcross progeny segregating this mutant phenotype confined Lps to a 0.9-cM interval spanning 1.7 Mb. Three transcription units were identified within the candidate interval, including Toll-like receptor 4 (Tlr4), part of a protein family with members that have been implicated in LPS-induced cell signaling. C3H/HeJ mice have a point mutation within the coding region of the Tlr4 gene, resulting in a nonconservative substitution of a highly conserved proline by histidine at codon 712, whereas C57BL/ 10ScCr mice exhibit a deletion of Tlr4. Identification of distinct mutations involving the same gene at the Lps locus in two different hyporesponsive inbred mouse strains strongly supports the hypothesis that altered Tlr4 function is responsible for endotoxin tolerance.

Key words: lipopolysaccharide;  inflammation;  positional cloning;  Salmonella;  mice/ inbred C3H


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