Inhibition of Adipogenesis by Ghrelin
-
Published:2004-05
Issue:5
Volume:15
Page:2484-2491
-
ISSN:1059-1524
-
Container-title:Molecular Biology of the Cell
-
language:en
-
Short-container-title:MBoC
Author:
Zhang Weizhen1, Zhao Lili1, Lin Theodore R.1, Chai Biaoxin1, Fan Yongyi1, Gantz Ira1, Mulholland Michael W.1
Affiliation:
1. Department of Surgery, Michigan Gastrointestinal Peptide Center, University of Michigan, Ann Arbor, Michigan 48109
Abstract
Ghrelin, a novel gastric hormone, regulates food intake and energy metabolism via central mechanisms. The peripheral effect of ghrelin on adiposity is poorly understood. We established a stable 3T3-L1 cell line expressing ghrelin to study the direct effect of ghrelin on adipogenesis. Cells overexpressing ghrelin demonstrate significantly attenuated differentiation of preadipocytes into adipocytes. Expression of peroxisome proliferator-activator receptor-γ is significantly inhibited as demonstrated by decrease of peroxisome proliferator-activator receptor-γ mRNA and protein. Both ghrelin overexpression and exogenous ghrelin stimulate cell proliferation. Phosphorylation of mitogen-activated protein kinase is increased after treatment of cells with ghrelin. Ghrelin binding activity is demonstrated in both native and ghrelin-overexpressing 3T3-L1 cells by radiolabeled ghrelin, although reverse transcription-polymerase chain reaction with the primer sequence of the previously identified ghrelin receptor subtypes detected no signal. Our results demonstrate that ghrelin inhibits adipogenesis by stimulation of cell proliferation via the mediation of a ghrelin receptor, likely a novel unidentified subtype.
Publisher
American Society for Cell Biology (ASCB)
Subject
Cell Biology,Molecular Biology
Reference32 articles.
1. Altiok, S.M., Xu, M., and Spiegelman, B.M. (1997). PPARgamma induces cell cycle withdrawal: inhibition of E2F/DP DNA-binding activity via down-regulation of PP2A.Genes Dev.11, 1987–1998. 2. Baldanzi, G.et al.(2002). Ghrelin and des-acyl ghrelin inhibit cell death in cardiomyocytes and endothelial cells through ERK1/2 and PI 3-kianse/AKT.J. Cell Biol.159, 1029–1037. 3. Banks, W.A., Tschop, M., and Heiman, M.L. (2002). Extent and direction of ghrelin transport across the blood brain barrier is determined by its unique primary structure.J. Pharmacol. Exp. Ther.302, 822–827. 4. Camp, H.S., and Tafuri, S.R. (1997). Regulation of peroxisome proliferators-activated receptor γ activity by mitogen-activated protein kinase.J. Biol. Chem.272, 10811–10816. 5. Cassoni, P., Papotti, M., Ghe, C., Catapano, F., Sapino, A., Graziani, A., Deghenghi, R., Reissmann, T., Ghigo, E., and Muccioli, G. (2000). Identification, characterization, and biological activity of specific receptors for natural (ghrelin) and synthetic growth hormone secretagogues and analogs in human breast carcinomas and cell lines.J. Clin. Endocrinol. Metab.86, 1738–1745.
Cited by
93 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|