Somatostatin modulates PI3K-Akt, eNOS and NHE activity in the ciliary epithelium

被引:12
作者
Ghosh, Sikha
Choritz, Lars
Geibel, John
Coca-Prados, Miguel
机构
[1] Yale Univ, Sch Med, Dept Ophthalmol & Visual Sci, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Surg, New Haven, CT 06510 USA
关键词
somatostatin; PI3K/Akt pathway; eNOS phosphorylation; Na+/H+-exchanger (NHE); ciliary epithelium;
D O I
10.1016/j.mce.2006.05.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Somatostatin (SST) is a biologically active peptide produced in neuroendocrine cells. In the present study, we provide evidence of pro-SST and SST receptor (SSTR1 and 2A) mRNA expression in ocular ciliary epithelium (CE). SST or SST-like immunoreactivity was detected by radioimmunoassay in tissue extract from ciliary processes and in aqueous humor. The distinct immunolabeling of CE with SST and proprotein convertases PC1 and PC2 antibodies suggested a tissue and cell-specific processing of pro-SST. SST (10(-8) to 10(-4) M) added exogenously to the CE, elicited the following effects: (i) a dose-dependent attenuation of Na+/H+-exchanger (NHE) activity; (ii) up to a two-fold increase phosphorylation of p-Akt-Ser(473) and of p-eNOS-Ser(617), and (iii) lack of response on intracellular cyclic GMP production. LY294002, a PI3K-inhibitor, blocked SST-induced p-Akt-Ser(473) and partially p-eNOS-Ser(617), however, it did not reverse SST-induced NHE attenuation. Collectively, these results suggested involvement of SST in multiple intracellular signaling pathways in the CE. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:63 / 75
页数:13
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