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作 者:田春雷[1] 叶飞[1] 徐同江[1] 王胜[1] 王晓丹[1] 雷霆[1]
机构地区:[1]华中科技大学同济医学院附属同济医院神经外科,武汉430030
出 处:《中国临床神经外科杂志》2010年第10期607-610,共4页Chinese Journal of Clinical Neurosurgery
基 金:国家自然科学基金(NO.30672161)
摘 要:目的探讨生长激素释放肽-6(GHRP-6)对大鼠生长激素腺瘤细胞GH3细胞cAMP反应元件结合蛋白(CREB)磷酸化水平的影响及其细胞内信号传导机制。方法用GHRP-6处理大鼠生长激素腺瘤GH3细胞并检测其对GH3细胞CREB磷酸化水平的影响;初步筛选参与GHRP-6激活的细胞内信号通路的蛋白激酶C(PKC)亚型;然后应用RNA干扰技术确认发挥中介作用的PKC亚型;Western免疫印迹法检测蛋白质磷酸化水平。结果 GHRP-6诱导的CREB磷酸化呈时间依赖性;PKCσ特殊抑制剂楸毒素可以明显减弱GHRP-6的这种效应;PKCσ表达沉默后GHRP-6诱导的CREB磷酸化水平明显降低;并且GHRP-6可以诱导PKCσ磷酸化。结论 PKC,特别是PKCσ,介导了GHRP-6诱导的CREB磷酸化。此结果为了解垂体生长激素腺瘤细胞内信号通路间"交叉通讯"提供了新的依据。Objective To explore the effect of growth hormone releasing peptide-6 (GHRP-6) on the phosphorylation level of cAMP response element binding protein(CREB) in GH3 cells of rat growth hormone(GH)-seereting adenoma and intracellular signal transduction mechanism of GHRP-6-induced CREB phosphorylation. Methods The level of CREB phosphorylation in the cultured GH3 cells of rats GH-secreling adenomas was determined after GHRP-6 treatment. Protein kinase C(PKC) subtype involved in GHRP-6-induced CREB phosphorylation was examined by RNA interference. CREB phosphorylafion and the PKC subtype activation were determined by Western blot. Results GHRP-6-induced CREB phosphorylation was time-dependent. The level of GHRP-6-induced CREB phosphorylation was significantly reduced by rottlerin, a special PKCσ inhibitor (P〈0.01). A dominant negative mutant of PKCσ also significantly reduced the level of GHRP-6-induced CREB phosphorylafion (P〈0.01). PKCσ activation was induced by GHRP-6 in time-dependent manner. Conclusion PKCσ may mediate CREB phosphorylation induced by GHRP-6 in GH3 cells. This result provides new basis for understanding the "cross talk" between signal paths in GH-seereting adenoma cells.
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