Chemerin enhances insulin signaling and potentiates insulin-stimulated glucose uptake in 3T3-L1 adipocytes

FEBS Letters

Volumn 582, Issue 5, 2008, Pages 573-578

  Takahashi, Michiko ^a   Takahashi, Yutaka ^a   Takahashi, Kenichi ^b   Zolotaryov, Fyodor N ^b   Hong, Kyoung Su ^b   Kitazawa, Riko ^a   Iida, Keiji ^a   Okimura, Yasuhiko ^c   Kaji, Hidesuke ^d   Kitazawa, Sohei ^a   Kasuga, Masato ^a   Chihara, Kazuo ^a  

^a KOBE UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b JCR Pharmaceuticals Co Ltd   (Japan)

^c KOBE UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^d UNIVERSITY OF HYOGO   (Japan)

Author keywords

3T3 L1 adipocyte; Adipocyte differentiation; Adipokine; Chemerin; Insulin sensitivity; Insulin signaling

Indexed keywords

ADIPOCYTOKINE; CELL PROTEIN; CHEMR23 RECEPTOR; INSULIN; PROTEIN CHEMERIN; RECEPTOR PROTEIN; UNCLASSIFIED DRUG;

ADIPOCYTE; ADIPOSE TISSUE; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; AUTOCRINE EFFECT; CELL DIFFERENTIATION; CELL STRAIN 3T3; CONTROLLED STUDY; GLUCOSE TRANSPORT; IN VIVO STUDY; INSULIN SENSITIVITY; LIVER; MOUSE; NONHUMAN; NORTHERN BLOTTING; PARACRINE SIGNALING; PRIORITY JOURNAL; PROTEIN EXPRESSION; TISSUE DISTRIBUTION;

3T3-L1 CELLS; ADIPOCYTES; ADIPOSE TISSUE; ANIMALS; ANTIBODY SPECIFICITY; CELL DIFFERENTIATION; CERCOPITHECUS AETHIOPS; CHEMOTACTIC FACTORS; COS CELLS; CULTURE MEDIA; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION; GLUCOSE; HUMANS; INSULIN; INTERCELLULAR SIGNALING PEPTIDES AND PROTEINS; LIVER; MALE; MICE; MICE, INBRED C57BL; SIGNAL TRANSDUCTION;

MUS;

EID: 39649114784     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.febslet.2008.01.023     Document Type: Article

References (29)

1. Zimmet P., Alberti K.G., and Shaw J. Global and societal implications of the diabetes epidemic. Nature 414 (2001) 782-787
2. Fantuzzi G. Adipose tissue, adipokines, and inflammation. J. Allergy Clin. Immunol. 115 (2005) 911-919 quiz 920
3. Kershaw E.E., and Flier J.S. Adipose tissue as an endocrine organ. J. Clin. Endocrinol. Metab. 89 (2004) 2548-2556
4. Charo I.F., and Taubman M.B. Chemokines in the pathogenesis of vascular disease. Circ. Res. 95 (2004) 858-866
5. Rossi D., and Zlotnik A. The biology of chemokines and their receptors. Annu. Rev. Immunol. 18 (2000) 217-242
6. Green H., and Kehinde O. An established preadipose cell line and its differentiation in culture. II. Factors affecting the adipose conversionc. Cell 5 (1975) 19-27
7. Nagpal S., et al. Tazarotene-induced gene 2 (TIG2), a novel retinoid-responsive gene in skin. J. Invest. Dermatol. 109 (1997) 91-95
8. Wittamer V., et al. Specific recruitment of antigen-presenting cells by chemerin, a novel processed ligand from human inflammatory fluids. J. Exp. Med. 198 (2003) 977-985
9. Zabel B.A., Allen S.J., Kulig P., Allen J.A., Cichy J., Handel T.M., and Butcher E.C. Chemerin activation by serine proteases of the coagulation, fibrinolytic, and inflammatory cascades. J. Biol. Chem. 280 (2005) 34661-34666
10. Zabel B.A., Silverio A.M., and Butcher E.C. Chemokine-like receptor 1 expression and chemerin-directed chemotaxis distinguish plasmacytoid from myeloid dendritic cells in human blood. J. Immunol. 174 (2005) 244-251
11. Goralski K.B., McCarthy T.C., Hanniman E.A., Zabel B.A., Butcher E.C., Parlee S.D., Muruganandan S., and Sinal C.J. Chemerin: A novel adipokine that regulates adipogenesis and adipocyte metabolism. J. Biol. Chem. 282 (2007) 28175-28188
12. Bozaoglu K., Bolton K., McMillan J., Zimmet P., Jowett J., Collier G., Walder K., and Segal D. Chemerin is a novel adipokine associated with obesity and metabolic syndrome. Endocrinology 148 (2007) 4687-4694
13. Roh S.G., Song S.H., Choi K.C., Katoh K., Wittamer V., Parmentier M., and Sasaki S. Chemerin-a new adipokine that modulates adipogenesis via its own receptor. Biochem. Biophys. Res. Commun. 362 (2007) 1013-1018
14. Green H., and Kehinde O. Spontaneous heritable changes leading to increased adipose conversion in 3T3 cells. Cell 7 (1976) 105-113
15. Mizuno I., Takahashi Y., Okimura Y., Kaji H., and Chihara K. Upregulation of the klotho gene expression by thyroid hormone and during adipose differentiation in 3T3-L1 adipocytes. Life Sci. 68 (2001) 2917-2923
16. Maebayashi Y., Shigeyoshi Y., Takumi T., and Okamura H. A putative transcription factor with seven zinc-finger motifs identified in the developing suprachiasmatic nucleus by the differential display PCR method. J. Neurosci. 19 (1999) 10176-10183
17. Takahashi M., et al. CXCL14 enhances insulin-dependent glucose uptake in adipocytes and is related to high-fat diet-induced obesity. Biochem. Biophys. Res. Commun. 364 (2007) 1037-1042
18. Takahashi Y., Carpino N., Cross J.C., Torres M., Parganas E., and Ihle J.N. SOCS3: an essential regulator of LIF receptor signaling in trophoblast giant cell differentiation. Embo J. 22 (2003) 372-384
19. Tachibana K., et al. Two cell adhesion molecules, nectin and cadherin, interact through their cytoplasmic domain-associated proteins. J. Cell Biol. 150 (2000) 1161-1176
20. Takahashi Y., Kaji H., Okimura Y., Goji K., Abe H., and Chihara K. Brief report: short stature caused by a mutant growth hormone. New Engl. J. Med. 334 (1996) 432-436
21. Takahashi Y., Okimura Y., Mizuno I., Iida K., Takahashi T., Kaji H., Abe H., and Chihara K. Leptin induces mitogen-activated protein kinase-dependent proliferation of C3H10T1/2 cells. J. Biol. Chem. 272 (1997) 12897-12900
22. Kishimoto K., Kitazawa R., Kurosaka M., Maeda S., and Kitazawa S. Expression profile of genes related to osteoclastogenesis in mouse growth plate and articular cartilage. Histochem. Cell Biol. 125 (2006) 593-602
23. Takahashi Y., et al. Growth hormone reverses nonalcoholic steatohepatitis in a patient with adult growth hormone deficiency. Gastroenterology 132 (2007) 938-943
24. Parmentier M. Characterization of new chemoattractant agents in leukocytes. Bull. Mem. Acad. R Med. Belg. 159 (2004) 515-520 discussion 521
25. Samson M., et al. ChemR23, a putative chemoattractant receptor, is expressed in monocyte-derived dendritic cells and macrophages and is a coreceptor for SIV and some primary HIV-1 strains. Eur. J. Immunol. 28 (1998) 1689-1700
26. Wittamer V., Gregoire F., Robberecht P., Vassart G., Communi D., and Parmentier M. The C-terminal nonapeptide of mature chemerin activates the chemerin receptor with low nanomolar potency. J. Biol. Chem. 279 (2004) 9956-9962
27. Xu H., et al. Chronic inflammation in fat plays a crucial role in the development of obesity-related insulin resistance. J. Clin. Invest. 112 (2003) 1821-1830
28. Weisberg S.P., McCann D., Desai M., Rosenbaum M., Leibel R.L., and Ferrante Jr. A.W. Obesity is associated with macrophage accumulation in adipose tissue. J. Clin. Invest. 112 (2003) 1796-1808
29. Wellen K.E., and Hotamisligil G.S. Obesity-induced inflammatory changes in adipose tissue. J. Clin. Invest. 112 (2003) 1785-1788