Dickkopf-1 promotes the differentiation and adipocytokines secretion via canonical Wnt signaling pathway in primary cultured human preadipocytes

Obesity Research and Clinical Practice

Volumn 10, Issue 4, 2016, Pages 454-464

  Lu, Hongyun ^a,b   Li, Xiaofeng ^a   Mu, Panwei ^a   Qian, Baiying ^b   Jiang, Wei ^a   Zeng, Longyi ^a  

^a THE THIRD AFFILIATED HOSPITAL OF SUN YAT SEN UNIVERSITY   (China)

^b THE FIFTH AFFILIATED HOSPITAL OF SUN YAT SEN UNIVERSITY   (China)

Author keywords

Adipocytokines secretion; Dickkopf 1; Differentiation; Human adipose derived stem cells (ASCs); Wnt signaling pathway

Indexed keywords

2 (2,4 DICHLOROPHENYL) 3 (1 METHYL 3 INDOLYL)MALEIMIDE; ADIPOCYTOKINE; ADIPONECTIN; BETA CATENIN; CCAAT ENHANCER BINDING PROTEIN ALPHA; DICKKOPF 1 PROTEIN; LEPTIN; LIPID; MESSENGER RNA; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR GAMMA; RECOMBINANT PROTEIN; RETINOL BINDING PROTEIN 4; TUMOR NECROSIS FACTOR; WNT10B PROTEIN; WNT3A PROTEIN; WNT5A PROTEIN; CCAAT ENHANCER BINDING PROTEIN; CEBPA PROTEIN, HUMAN; DKK1 PROTEIN, HUMAN; PLASMA RETINOL BINDING PROTEIN; RBP4 PROTEIN, HUMAN; SIGNAL PEPTIDE; WNT PROTEIN;

ADIPOCYTE; ADIPOGENESIS; ADIPOSE TISSUE; ADULT; ARTICLE; CELL DIFFERENTIATION; CELL ISOLATION; CLINICAL ARTICLE; CONTROLLED STUDY; CYTOKINE RELEASE; DOWN REGULATION; ENZYME LINKED IMMUNOSORBENT ASSAY; GENE EXPRESSION PROFILING; HUMAN; HUMAN CELL; HUMAN TISSUE; LIPOGENESIS; LIPOLYSIS; PRIORITY JOURNAL; PROADIPOCYTE; PROTEIN EXPRESSION; PROTEIN FUNCTION; QUANTITATIVE ANALYSIS; REAL TIME POLYMERASE CHAIN REACTION; UPREGULATION; WESTERN BLOTTING; WNT SIGNALING PATHWAY; CELL CULTURE; CYTOLOGY; LIPID METABOLISM; METABOLISM; OBESITY; SECRETION (PROCESS); WNT SIGNALING;

ADIPOCYTES; ADIPOGENESIS; ADIPOKINES; ADIPOSE TISSUE; BETA CATENIN; CCAAT-ENHANCER-BINDING PROTEINS; CELL DIFFERENTIATION; CELLS, CULTURED; HUMANS; INTERCELLULAR SIGNALING PEPTIDES AND PROTEINS; LIPID METABOLISM; OBESITY; PPAR GAMMA; RETINOL-BINDING PROTEINS, PLASMA; TUMOR NECROSIS FACTOR-ALPHA; WNT PROTEINS; WNT SIGNALING PATHWAY;

EID: 84941687288     PISSN: 1871403X     EISSN: 18780318     Source Type: Journal    
DOI: 10.1016/j.orcp.2015.08.016     Document Type: Article

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