Shimizu H, Ohtani K, Tsuchiya T, Takahashi H, Uehara Y, Sato N, Mori M
First Department of Internal Medicine, Gunma University School of Medicine, Maebashi, Japan.
Peptides. 1997;18(8):1263-6. doi: 10.1016/s0196-9781(97)00137-x.
Leptin, an ob gene product, corrects hyperinsulinemia in ob/ob mice. The leptin receptor may exist in pancreatic islets. The present studies were undertaken to determine the direct effect of 1-100 ng/ml recombinant leptin on insulin secretion and synthesis in HIT-T 15 cells by using static culture system. The addition of recombinant leptin significantly increased insulin secretion for 20 min at the highest concentration (100 ng/ml). The addition of recombinant leptin dose-dependently increased insulin secretion for 24 h in the 7 mM glucose-containing F-12 K medium. The incubation with recombinant leptin for 24 h increased preproinsulin mRNA expression, assessed with reverse transcription-polymerase chain reaction (RT-PCR) method. It was furthermore demonstrated that HIT-T 15 cells possessed the specific binding site for [125I]-labeled leptin. The present study demonstrated the existence of the leptin-specific binding sites that mediate its stimulatory effect on insulin secretion and synthesis in HIT-T 15 cells.
瘦素是肥胖基因的产物,可纠正ob/ob小鼠的高胰岛素血症。瘦素受体可能存在于胰岛中。本研究旨在利用静态培养系统,确定1-100 ng/ml重组瘦素对HIT-T 15细胞胰岛素分泌和合成的直接影响。在最高浓度(100 ng/ml)下,添加重组瘦素可显著增加胰岛素分泌20分钟。在含7 mM葡萄糖的F-12 K培养基中,添加重组瘦素可在24小时内剂量依赖性地增加胰岛素分泌。用逆转录-聚合酶链反应(RT-PCR)方法评估,与重组瘦素孵育24小时可增加前胰岛素原mRNA表达。此外还证明,HIT-T 15细胞具有[125I]标记瘦素的特异性结合位点。本研究证明了瘦素特异性结合位点的存在,该位点介导其对HIT-T 15细胞胰岛素分泌和合成的刺激作用。