Cheng Henrique, Yibchok-anun Sirintorn, Coy David H, Hsu Walter H
Department of Biomedical Sciences, College of Veterinary Medicine, Iowa State University, Ames, IA 50011 USA.
Life Sci. 2002 Jul 12;71(8):927-36. doi: 10.1016/s0024-3205(02)01774-5.
The effects of somatostatin (SRIF) are mediated through the seven transmembrane receptor family that signals via Gi/Go. To date, five distinct SRIF receptors have been characterized and designated SSTR1-5. We have characterized the SRIF receptor that mediates the increase in Ca(2+) and insulin secretion in HIT-T15 cells (Simian virus 40-transformed Syrian hamster islets) using high affinity, subtype selective agonists for SSTR1 (L-797,591), SSTR2 (L-779,976), SSTR3 (L-796,778), SSTR4 (L-803,087), SSTR5 (L-817,818) and PRL-2903, a specific SSTR2 antagonist. In the presence of arginine vasopressin (AVP), SRIF increased Ca(2+) and insulin secretion. Treatment with the SSTR2 agonist L-779,976 resulted in similar responses to SRIF. In addition, L-779,976 increased both Ca(2+) and insulin secretion in a dose-dependent manner. Treatment with L-779,976 alone did not alter Ca(2+) or basal insulin secretion. In the presence of AVP, all other SRIF receptor agonists failed to increase Ca(2+) and insulin secretion. The effects of SRIF and L-779,976 were abolished by the SSTR2 antagonist PRL-2903. Our results suggest that the mechanism underlying SRIF-induced insulin secretion in HIT-T15 cells be mediated through the SSTR2.
生长抑素(SRIF)的作用是通过经由Gi/Go发出信号的七跨膜受体家族介导的。迄今为止,已鉴定出五种不同的SRIF受体,并命名为SSTR1 - 5。我们使用针对SSTR1(L - 797,591)、SSTR2(L - 779,976)、SSTR3(L - 796,778)、SSTR4(L - 803,087)、SSTR5(L - 817,818)的高亲和力、亚型选择性激动剂以及特异性SSTR2拮抗剂PRL - 2903,对介导HIT - T15细胞(猿猴病毒40转化的叙利亚仓鼠胰岛)中[Ca(2+)]i升高和胰岛素分泌的SRIF受体进行了鉴定。在存在精氨酸加压素(AVP)的情况下,SRIF增加了[Ca(2+)]i和胰岛素分泌。用SSTR2激动剂L - 779,976处理产生了与SRIF相似的反应。此外,L - 779,976以剂量依赖性方式增加了[Ca(2+)]i和胰岛素分泌。单独用L - 779,976处理未改变[Ca(2+)]i或基础胰岛素分泌。在存在AVP的情况下,所有其他SRIF受体激动剂均未能增加[Ca(2+)]i和胰岛素分泌。SRIF和L - 779,976的作用被SSTR2拮抗剂PRL - 2903消除。我们的结果表明,SRIF诱导HIT - T15细胞胰岛素分泌的机制是通过SSTR2介导的。