Zhang Weizhen, Zhao Lili, Lin Theodore R, Chai Biaoxin, Fan Yongyi, Gantz Ira, Mulholland Michael W
Department of Surgery, Michigan Gastrointestinal Peptide Center, University of Michigan, Ann Arbor, MI 48109, USA.
Mol Biol Cell. 2004 May;15(5):2484-91. doi: 10.1091/mbc.e03-09-0657. Epub 2004 Mar 19.
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-gamma is significantly inhibited as demonstrated by decrease of peroxisome proliferator-activator receptor-gamma 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.
胃饥饿素是一种新型胃激素,通过中枢机制调节食物摄入和能量代谢。胃饥饿素对肥胖的外周作用尚不清楚。我们建立了一种表达胃饥饿素的稳定3T3-L1细胞系,以研究胃饥饿素对脂肪生成的直接作用。过表达胃饥饿素的细胞显示前脂肪细胞向脂肪细胞的分化明显减弱。过氧化物酶体增殖物激活受体γ的表达受到显著抑制,表现为过氧化物酶体增殖物激活受体γ mRNA和蛋白水平降低。胃饥饿素过表达和外源性胃饥饿素均刺激细胞增殖。用胃饥饿素处理细胞后,丝裂原活化蛋白激酶的磷酸化增加。通过放射性标记的胃饥饿素在天然和过表达胃饥饿素的3T3-L1细胞中均显示出胃饥饿素结合活性,尽管使用先前鉴定的胃饥饿素受体亚型的引物序列进行逆转录-聚合酶链反应未检测到信号。我们的结果表明,胃饥饿素通过胃饥饿素受体介导刺激细胞增殖来抑制脂肪生成,该受体可能是一种新型未鉴定的亚型。