Yan Jing, Zhao Wenhui, Guo Meixia, Han Xuefei, Feng Zhiwei
Xinxiang medical university, Xinxiang, China.
Cell Physiol Biochem. 2016;40(5):982-992. doi: 10.1159/000453155. Epub 2016 Dec 7.
CXCL12 is pivotal for cholinergic neurons, and it induces the expressions of several genes that are essential for synthesis and storage of acetylcholine(ACh), specifically choline acetyltransferase, vesicular ACh transporter (VAChT), and choline transporter. The present study explored the impact of pharmacological Akt inhibition upon cholinergic gene expression.
Western blotting was employed to determine the level of p-AKT, RT-PCR to check the mRNA levels of and CHT1(choline transporter1),VAChT and ChAT, ELISA to decipher the secretion of ACh and the activity of choline acetyltransferase.
Here we demonstrated, in the rat pheochromocytoma cell line PC12 and in primary rat neuronal cultures, that CXCL12-evoked up-regulation of CHT1, VAChT and ChAT was mediated by Akt. Inhibition of Akt by the pharmacological inhibitor GSK690693 eliminated CXCL12-stimulated increases in cholinergic gene expression. Moreover, treatment with GSK690693 reversed CXCL12-evoked increases in choline acetyltransferase activity and ACh production.
Our results suggest that CXCL12 contributes to cholinergic gene expression via Akt signaling pathway.
CXCL12对胆碱能神经元至关重要,它能诱导几种对乙酰胆碱(ACh)合成和储存必不可少的基因的表达,特别是胆碱乙酰转移酶、囊泡型乙酰胆碱转运体(VAChT)和胆碱转运体。本研究探讨了药理学上抑制Akt对胆碱能基因表达的影响。
采用蛋白质免疫印迹法测定p-AKT水平,逆转录聚合酶链反应检测胆碱转运体1(CHT1)、VAChT和胆碱乙酰转移酶(ChAT)的mRNA水平,酶联免疫吸附测定法解析ACh的分泌及胆碱乙酰转移酶的活性。
我们在大鼠嗜铬细胞瘤细胞系PC12和原代大鼠神经元培养物中证实,CXCL12引起的CHT1、VAChT和ChAT的上调是由Akt介导的。药理学抑制剂GSK690693抑制Akt可消除CXCL12刺激的胆碱能基因表达增加。此外,用GSK690693处理可逆转CXCL12引起的胆碱乙酰转移酶活性和ACh产生的增加。
我们的结果表明,CXCL12通过Akt信号通路促进胆碱能基因表达。