Wente Wolf, Efanov Alexander M, Treinies Iris, Zitzer Heike, Gromada Jesper, Richter Dietmar, Kreienkamp Hans-Jürgen
Lilly Research Laboratories, Essener Bogen 7, D-22419 Hamburg, Germany.
FEBS Lett. 2005 Nov 21;579(28):6305-10. doi: 10.1016/j.febslet.2005.10.009. Epub 2005 Oct 21.
The multi-domain protein PIST (protein interacting specifically with Tc10) interacts with the SSTR5 (somatostatin receptor 5) and is responsible for its intracellular localization. Here, we show that PIST is expressed in pancreatic beta-cells and interacts with SSTR5 in these cells. PIST expression in MIN6 insulinoma cells is reduced by somatostatin (SST). After stimulation with SST, SSTR5 undergoes internalization together with PIST. MIN6 cells over-expressing PIST display enhanced glucose-stimulated insulin secretion and a decreased sensitivity to SST-induced inhibition of insulin secretion. These data suggest that PIST plays an important role in insulin secretion by regulating SSTR5 availability at the plasma membrane.
多结构域蛋白PIST(与Tc10特异性相互作用的蛋白)与生长抑素受体5(SSTR5)相互作用,并负责其细胞内定位。在此,我们表明PIST在胰腺β细胞中表达,并在这些细胞中与SSTR5相互作用。生长抑素(SST)可降低MIN6胰岛素瘤细胞中PIST的表达。用SST刺激后,SSTR5与PIST一起发生内化。过表达PIST的MIN6细胞显示出增强的葡萄糖刺激的胰岛素分泌,以及对SST诱导的胰岛素分泌抑制的敏感性降低。这些数据表明,PIST通过调节质膜上SSTR5的可用性,在胰岛素分泌中发挥重要作用。