Endogenous HMGB1 is required in endotoxin tolerance

Journal of Surgical Research

Volumn 185, Issue 1, 2013, Pages 319-328

  Li, Shanshan ^a   Luo, Chengqun ^a   Yin, Chaoqi ^a   Peng, Chen ^a   Han, Rong ^b   Zhou, Jun ^a   He, Quangyong ^a   Zhou, Jianda ^a  

^a CENTRAL SOUTH UNIVERSITY   (China)

^b BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

HMGB1 protein; Immune tolerance; Inflammation; IRAK M; Lipopolysaccharide; Nuclear factor B

Indexed keywords

ENDOTOXIN; HIGH MOBILITY GROUP B1 PROTEIN; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; INTERLEUKIN 1 RECEPTOR; LIPOPOLYSACCHARIDE; PROTEIN ANTIBODY; TUMOR NECROSIS FACTOR ALPHA;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; ENDOTOXEMIA; LIVER; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN SECRETION; PROTEIN TRANSPORT; SIGNAL TRANSDUCTION;

HMGB1 PROTEIN; IMMUNE TOLERANCE; INFLAMMATION; IRAK-M; LIPOPOLYSACCHARIDE; NUCLEAR FACTOR ΚB;

ANIMALS; AUTOANTIBODIES; CELL LINE; DISEASE MODELS, ANIMAL; ENDOTOXEMIA; HMGB1 PROTEIN; IMMUNE TOLERANCE; INFLAMMATION MEDIATORS; INTERLEUKIN-1; INTERLEUKIN-1 RECEPTOR-ASSOCIATED KINASES; LIPOPOLYSACCHARIDES; MACROPHAGES; MALE; MICE; MICE, INBRED BALB C; SEPSIS; SIGNAL TRANSDUCTION; TUMOR NECROSIS FACTOR-ALPHA;

EID: 84886726303     PISSN: 00224804     EISSN: 10958673     Source Type: Journal    
DOI: 10.1016/j.jss.2013.05.062     Document Type: Article

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