Adipolin/C1qdc2/CTRP12 protein functions as an adipokine that improves glucose metabolism

Journal of Biological Chemistry

Volumn 286, Issue 40, 2011, Pages 34552-34558

  Enomoto, Takashi ^a   Ohashi, Koji ^a   Shibata, Rei ^a   Higuchi, Akiko ^b   Maruyama, Sonomi ^a   Izumiya, Yasuhiro ^b   Walsh, Kenneth ^b   Murohara, Toyoaki ^a   Ouchi, Noriyuki ^a  

^a NAGOYA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

3T3-L1 ADIPOCYTES; ADIPOKINES; ADIPOSE TISSUE; ANTI-INFLAMMATORIES; BIOACTIVE MOLECULES; CONDITIONED MEDIUM; ENDOPLASMIC RETICULUM STRESS; FAT TISSUE; GLUCOSE HOMEOSTASIS; GLUCOSE INTOLERANCE; GLUCOSE METABOLISM; INFLAMMATORY RESPONSE; INSULIN RESISTANCE; OBESE MICE; PROINFLAMMATORY; PROINFLAMMATORY CYTOKINES; PROTEIN FUNCTIONS; RISK FACTORS; RODENT MODELS; SYSTEMIC ADMINISTRATION; TARGET MOLECULE; TYPE-2 DIABETES;

GLUCOSE; INSULIN; MACROPHAGES; MAMMALS; METABOLISM; MOLECULES; NUTRITION; PHYSIOLOGY; TISSUE;

GENE EXPRESSION;

ADIPOCYTOKINE; ADIPOLIN; GLUCOSE; LIPOPOLYSACCHARIDE; MESSENGER RNA; PROTEIN C1QDC2; PROTEIN CTRP12; TUMOR NECROSIS FACTOR ALPHA; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL STIMULATION; CELL STRAIN 3T3; CONTROLLED STUDY; CULTURE MEDIUM; DIABETES MELLITUS; DIETARY INTAKE; ENDOPLASMIC RETICULUM STRESS; GENE EXPRESSION; GLUCOSE INTOLERANCE; GLUCOSE METABOLISM; IN VIVO STUDY; INFLAMMATION; INSULIN RESISTANCE; MACROPHAGE; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; OBESITY; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN BLOOD LEVEL; PROTEIN EXPRESSION; PROTEIN FUNCTION; WHITE ADIPOSE TISSUE;

3T3-L1 CELLS; ADIPOKINES; ANIMALS; CERCOPITHECUS AETHIOPS; CLONING, MOLECULAR; COS CELLS; ENDOPLASMIC RETICULUM; GLUCOSE; INFLAMMATION; LIPOPOLYSACCHARIDES; MACROPHAGES; MALE; MICE; MICE, INBRED C57BL; MODELS, BIOLOGICAL; OBESITY; TUMOR NECROSIS FACTOR-ALPHA;

MUS; RODENTIA;

EID: 80053413113     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M111.277319     Document Type: Article

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