Kagimoto S, Yamada Y, Kubota A, Someya Y, Ihara Y, Yasuda K, Kozasa T, Imura H, Seino S, Seino Y
Department of Metabolism and Clinical Nutrition, Kyoto University Faculty of Medicine, Japan.
Biochem Biophys Res Commun. 1994 Jul 29;202(2):1188-95. doi: 10.1006/bbrc.1994.2054.
Somatostatin has been shown to exert diverse biological effects in various tissues. Recently, the human genes encoding five subtypes of somatostatin receptor (SSTR1-SSTR5) were cloned. Among these subtypes SSTR2 is present in many endocrine tumors as well as normal tissues and may mediate the effects of somatostatin analog, SMS201-995. In this study, we have investigated the intracellular effect of SSTR2 stably expressed in Chinese hamster ovary cells. Somatostatin-14 does not affect the forskolin stimulated cAMP formation when human SSTR2 is expressed in CHO cells, which lack internal Gi alpha 1 protein. However, somatostatin-14 inhibits the adenylyl cyclase in a dose dependent and pertussis toxin-sensitive manner when human SSTR2 is co-expressed with Gi alpha 1 in CHO cells. These results indicate that human SSTR2 is functionally coupled to Gi alpha 1 protein but not to Gi alpha 2 or Gi alpha 3 when expressed in CHO cells.
生长抑素已被证明在各种组织中发挥多种生物学作用。最近,编码生长抑素受体五种亚型(SSTR1 - SSTR5)的人类基因被克隆出来。在这些亚型中,SSTR2存在于许多内分泌肿瘤以及正常组织中,并且可能介导生长抑素类似物SMS201 - 995的作用。在本研究中,我们研究了在中国仓鼠卵巢细胞中稳定表达的SSTR2的细胞内效应。当人类SSTR2在缺乏内源性Giα1蛋白的CHO细胞中表达时,生长抑素 - 14不影响福斯高林刺激的cAMP形成。然而,当人类SSTR2与Giα1在CHO细胞中共表达时,生长抑素 - 14以剂量依赖性和百日咳毒素敏感的方式抑制腺苷酸环化酶。这些结果表明,人类SSTR2在CHO细胞中表达时在功能上与Giα1蛋白偶联,而不与Giα2或Giα3偶联。