Negative Regulation of Pancreatic and Duodenal Homeobox-1 by Somatostatin Receptor Subtype 5

被引:16
|
作者
Zhou, Guisheng [1 ,6 ]
Liu, Shi-He [1 ,6 ]
Shahi, Kelly M. [6 ]
Wang, Hua [4 ]
Duan, Xueyan [6 ]
Lin, Xia [6 ]
Feng, Xin-Hua [6 ]
Li, Min [3 ]
Fisher, William E. [6 ]
DeMayo, Francesco J. [5 ]
Dawson, David [2 ]
Brunicardi, F. Charles [1 ,6 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Surg, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
[3] Univ Texas Houston, Sch Med, Vivian L Smith Dept Neurosurg, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX 77030 USA
[5] Univ Texas MD Anderson Canc Ctr, Baylor Coll Med, Dept Mol & Cell Biol, Houston, TX 77030 USA
[6] Univ Texas MD Anderson Canc Ctr, Michael E DeBakey Dept Surg, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
GLUCAGON-LIKE PEPTIDE-1; INSULIN GENE-TRANSCRIPTION; PROLIFERATION IN-VITRO; DNA-BINDING ACTIVITY; NEUROENDOCRINE TUMORS; PROTEIN-KINASE; PHOSPHATIDYLINOSITOL; 3-KINASE; CELL-DIFFERENTIATION; ENDOCRINE PANCREAS; PDX-1; EXPRESSION;
D O I
10.1210/me.2012-1095
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Somatostatin receptor subtype 5 (SSTR5) mediates the inhibitory effect of somatostatin and its analogs on insulin expression/secretion and islet cell proliferation. We provide biochemical and genetic evidence that SSTR5 exerted its physiological actions via down-regulating pancreatic and duodenal homeobox-1 (PDX-1), a beta-cell-specific homeodomain-containing transcription factor. Cotransfection of SSTR5 with PDX-1 resulted in dose-dependent inhibition of PDX-1 expression in human embryonic kidney 293 cells. SSTR5 agonist RPL-1980 inhibited PDX-1 expression and abolished glucagon-like peptide 1-stimulated PDX-1 expression in mouse insulinoma beta-TC-6 cells. SSTR5 knockdown by short hairpin RNA led to increased PDX-1 expression that was accompanied by enhanced insulin secretion stimulated by high glucose in beta-TC6 cells and alternated expressions of cell cycle proteins that favor cell proliferation in mouse insulinoma MIN6 cells. Quantitative RT-PCR analysis showed that cotransfected SSTR5 inhibited PDX-1 mRNA expression, whereas knockdown of SSTR5 increased PDX-1 mRNA expression. In addition, we found that cotransfected wild-type SSTR5 increased PDX-1 ubiquitination in human embryonic kidney 293 cells, whereas SSTR5 P335L, a hypofunctional single nucleotide polymorphism of SSTR5, inhibited PDX-1 ubiquitination. SSTR5 knockout resulted in increased expression of PDX-1, insulin, and proliferating cell nuclear antigen in the islets of sstr(-/-) mice. Immunohistochemistry analysis showed that SSTR5 P335L was associated with elevated expression of PDX-1 in human pancreatic neuroendocrine tumor. Taken together, our studies demonstrated that SSTR5 is a negative regulator for PDX-1 expression and that SSTR5 may mediate the inhibitory effects of somatostatin and its analogs on insulin expression/secretion and cell proliferation via down-regulating PDX-1 at both transcriptional and posttranslational levels. (Molecular Endocrinology 26: 1225-1234, 2012)
引用
收藏
页码:1225 / 1234
页数:10
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