Suppr超能文献

生长抑素调节睫状体上皮中的PI3K-Akt、eNOS和NHE活性。

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

作者信息

Ghosh Sikha, Choritz Lars, Geibel John, Coca-Prados Miguel

机构信息

Department of Ophthalmology and Visual Science, Yale University School of Medicine, New Haven, CT 06510, USA.

出版信息

Mol Cell Endocrinol. 2006 Jul 11;253(1-2):63-75. doi: 10.1016/j.mce.2006.05.002. Epub 2006 Jun 9.

Abstract

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-Ser473 and of p-eNOS-Ser617, and (iii) lack of response on intracellular cyclic GMP production. LY294002, a PI3K-inhibitor, blocked SST-induced p-Akt-Ser473 and partially p-eNOS-Ser617, however, it did not reverse SST-induced NHE attenuation. Collectively, these results suggested involvement of SST in multiple intracellular signaling pathways in the CE.

摘要

生长抑素(SST)是一种在神经内分泌细胞中产生的生物活性肽。在本研究中,我们提供了眼部睫状体上皮(CE)中前SST和SST受体(SSTR1和2A)mRNA表达的证据。通过放射免疫分析法在睫状体组织提取物和房水中检测到SST或SST样免疫反应性。用SST以及前体蛋白转化酶PC1和PC2抗体对CE进行的不同免疫标记表明前SST存在组织和细胞特异性加工。将SST(10^(-8)至10^(-4)M)外源性添加到CE中,会引发以下效应:(i)Na+/H+交换体(NHE)活性呈剂量依赖性减弱;(ii)p-Akt-Ser473和p-eNOS-Ser617的磷酸化增加高达两倍,以及(iii)对细胞内环状GMP产生无反应。PI3K抑制剂LY294002阻断了SST诱导的p-Akt-Ser473和部分p-eNOS-Ser617,但并未逆转SST诱导的NHE减弱。总体而言,这些结果表明SST参与了CE中的多种细胞内信号通路。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验