Watanabe Hiroaki, Saito Hiroshi, Ueda Junji, Evers B Mark
Department of Surgery, The University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555-0536, USA.
Biochem Biophys Res Commun. 2008 May 23;370(1):33-7. doi: 10.1016/j.bbrc.2008.03.012. Epub 2008 Mar 11.
We have previously demonstrated that the phosphatidylinositol-3 kinase (PI3K)/Akt signaling is essential for pancreatic regeneration after partial pancreatectomy in mice. In the present study, we examined a role of PI3K/Akt signaling for pancreatic duct cell differentiation into insulin-producing cells. Epithelial-like cells were isolated from mouse pancreas and confirmed to be positive for a duct cell marker cytokeratin-20 (CK-20) but negative for insulin. Incubation of these cells with epidermal growth factor, exhibited a gradual increase in Akt phosphorylation and expression of pancreatic duodenal homeobox-1 (PDX-1), a regulator of beta-cell differentiation. Three weeks later, these CK-20-positive cells were noted to express insulin as determined by immunofluorescent double-staining. Akt phosphorylation, PDX-1 expression, and insulin production were effectively reduced by blocking the PI3K/Akt pathway using siRNA to the p85alpha regulatory subunit of PI3K. Our results demonstrate that PI3K/Akt activation has a critical role for pancreatic duct cell differentiation into insulin-producing cells.
我们之前已经证明,磷脂酰肌醇-3激酶(PI3K)/Akt信号传导对于小鼠部分胰腺切除术后的胰腺再生至关重要。在本研究中,我们研究了PI3K/Akt信号传导在胰腺导管细胞分化为胰岛素分泌细胞中的作用。从小鼠胰腺中分离出上皮样细胞,证实其对导管细胞标志物细胞角蛋白-20(CK-20)呈阳性,但对胰岛素呈阴性。用表皮生长因子孵育这些细胞后,Akt磷酸化和胰腺十二指肠同源盒-1(PDX-1,一种β细胞分化调节因子)的表达逐渐增加。三周后,通过免疫荧光双重染色确定,这些CK-20阳性细胞开始表达胰岛素。使用针对PI3K的p85α调节亚基的小干扰RNA(siRNA)阻断PI3K/Akt途径后,Akt磷酸化、PDX-1表达和胰岛素产生均有效降低。我们的结果表明,PI3K/Akt激活在胰腺导管细胞分化为胰岛素分泌细胞中起关键作用。