CCR2 deficiency leads to increased eosinophils, alternative macrophage activation, and type 2 cytokine expression in adipose tissue

Journal of Leukocyte Biology

Volumn 98, Issue 4, 2015, Pages 467-477

  Bolus, W Reid ^a   Gutierrez, Dario A ^a,c   Kennedy, Arion J ^a   Anderson Baucum, Emily K ^a,d   Hasty, Alyssa H ^a,b  

^a VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b VETERANS AFFAIRS MEDICAL CENTER   (United States)

^c GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

^d INDIANA UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Inflammation; Interleukin 5; Obesity

Indexed keywords

CD11B ANTIGEN; CHEMOKINE RECEPTOR CCR2; CHEMOKINE RECEPTOR CCR3; EOTAXIN; EOTAXIN 2; INDUCIBLE NITRIC OXIDE SYNTHASE; INTERLEUKIN 13; INTERLEUKIN 4; INTERLEUKIN 5; INTERLEUKIN 5 RECEPTOR ALPHA; INTERLEUKIN 6; MACROPHAGE INFLAMMATORY PROTEIN 1ALPHA; MESSENGER RNA; RANTES; TRANSCRIPTION FACTOR FOXP3; TRANSCRIPTION FACTOR GATA 1; TUMOR NECROSIS FACTOR ALPHA; CCR2 PROTEIN, MOUSE;

ADIPOSE TISSUE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; BLOOD; BONE MARROW; BONE MARROW CULTURE; CELL DIFFERENTIATION; CELL MIGRATION; CELL PROLIFERATION; CONTROLLED STUDY; EOSINOPHIL COUNT; GLUCOSE TOLERANCE; IN VITRO STUDY; LIVER; MACROPHAGE ACTIVATION; MALE; MOUSE; NONHUMAN; OBESITY; PERITONEAL CAVITY; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; REGULATORY T LYMPHOCYTE; WHITE ADIPOSE TISSUE; ANIMAL; BIOSYNTHESIS; C57BL MOUSE; CELL SEPARATION; EOSINOPHIL; FLOW CYTOMETRY; IMMUNOHISTOCHEMISTRY; IMMUNOLOGY; INFLAMMATION; INSULIN RESISTANCE; KNOCKOUT MOUSE; REAL TIME POLYMERASE CHAIN REACTION;

ADIPOSE TISSUE; ANIMALS; CELL SEPARATION; EOSINOPHILS; FLOW CYTOMETRY; IMMUNOHISTOCHEMISTRY; INFLAMMATION; INSULIN RESISTANCE; INTERLEUKIN-13; INTERLEUKIN-4; INTERLEUKIN-5; MACROPHAGE ACTIVATION; MALE; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; OBESITY; REAL-TIME POLYMERASE CHAIN REACTION; RECEPTORS, CCR2;

EID: 84943179861     PISSN: 07415400     EISSN: 19383673     Source Type: Journal    
DOI: 10.1189/jlb.3HI0115-018R     Document Type: Article

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