Carboxyl-terminal multi-site phosphorylation regulates internalization and desensitization of the human sst2 somatostatin receptor

MOLECULAR AND CELLULAR ENDOCRINOLOGY

卷:387

Article

Lehmann, Andreas¹  Kliewer, Andrea¹  Schuetz, Dagmar¹  Nagel, Falko¹  Stumm, Ralf¹  Schulz, Stefan¹ 

[1] Univ Jena, Jena Univ Hosp, Inst Pharmacol & Toxicol, D-07747 Jena, Germany

关键词: Somatostatin;    Octreotide;    Pasireotide;    Somatostatin receptor;    Internalization;    Desensitization;   

DOI  :  10.1016/j.mce.2014.02.009

来源: Elsevier

【 摘 要 】

The somatostatin receptor 2 (sst(2)) is the pharmacological target of somatostatin analogs that are widely used in the diagnosis and treatment of human neuroendocrine tumors. We have recently shown that the stable somatostatin analogs octreotide and pasireotide (SOM230) stimulate distinct patterns of sst(2) receptor phospholylation and internalization. Like somatostatin, octreotide promotes the phosphorylation of at least six carboxyl-terminal serine and threonine residues namely S341, S343, T353, T354, T356 and T359, which in turn leads to a robust receptor endocytosis. Unlike somatostatin, pasireotide stimulates a selective phosphorylation of S341 and S343 of the human sst(2) receptor followed by a partial receptor internalization. Here, we show that exchange of S341 and S343 by alanine is sufficient to block pasireotide-driven internalization, whereas mutation of T353, T354, T356 and T359 to alanine is required to strongly inhibited both octreotide- and somatostatin-induced internalization. Yet, combined mutation of T353, T354, T356 and T359 is not sufficient to prevent somatostatin-driven B-arrestin mobilization and receptor desensitization. Replacement of all fourteen carboxyl-terminal serine and threonine residues by alanine completely abrogates sst(2) receptor internalization and B-arrestin mobilization in HEK293 cells. Together, our findings demonstrate for the first time that agonist-selective sst(2) receptor internalization is regulated by multi-site phosphorylation of its carboxyl-terminal tail. (C) 2014 Elsevier Ireland Ltd. All rights reserved.

【 授权许可】

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