Wen Fangfang, Liu Leping, Xu Zhu, Yang Janjing, Ding Saidan
Zhejiang Provincial Key Laboratory of Aging and Neurological Disease Research, First Affiliated Hospital, Wenzhou Medical University, Wenzhou 325000, China.
Surgical Laboratory, First Affiliated Hospital, Wenzhou Medical University, Wenzhou 325000, China.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2017 Jul;33(7):930-935.
Objective To investigate the effect of dopamine (DA) on the glutamate (Glu)-uptake ability of astrocytes, and the role of trace amine-associated receptor 1-excitatory amino acid transporter 2 (TAAR1-EAAT2) signaling pathway in Glu uptake by astrocytes. Methods In the primary cultured astrocytes pretreated with DA, extracellular Glu levels were measured by the Amplex Red glutamic acid assay kit. The levels of TAAR1 and EAAT2 transcriptions were detected by reverse transcription PCR and their protein levels were analyzed by Western blotting. After TAAR1 plasmid and TAAR1 siRNA were separately transfected into the primary astrocytes pretreated by DA, Western blotting was performed to determine the level of EAAT2 and Amplex Red glutamic acid assay kit was used to analyze Glu uptake in primary cultured astrocyte supernatants. Results The expression of EAAT2 in the primary cultured astrocytes significantly decreased in response to DA, and the level of TAAR1 increased. DA significantly enhanced the Glu uptake in primary cultured astrocyte supernatants. After TAAR1 siRNA transfection, EAAT2 expression was upregulated by DA treatment and Glu content in the supernatants was downregulated. On the contrary, after TAAR1 plasmid transfection, EAAT2 expression descended and Glu level ascended in the supernatants. Conclusion DA reduces the Glu-uptake ability of astrocytes through TAAR1-EAAT2 signaling pathway, causes extracellular Glu accumulation, and ultimately destroys the function of astrocytes.
目的 探讨多巴胺(DA)对星形胶质细胞谷氨酸(Glu)摄取能力的影响,以及痕量胺相关受体1-兴奋性氨基酸转运体2(TAAR1-EAAT2)信号通路在星形胶质细胞摄取Glu中的作用。方法 用DA预处理原代培养的星形胶质细胞后,采用Amplex Red谷氨酸检测试剂盒测定细胞外Glu水平。通过逆转录PCR检测TAAR1和EAAT2转录水平,并用蛋白质免疫印迹法分析其蛋白水平。将TAAR1质粒和TAAR1小干扰RNA(siRNA)分别转染至经DA预处理的原代星形胶质细胞后,进行蛋白质免疫印迹法检测EAAT2水平,并用Amplex Red谷氨酸检测试剂盒分析原代培养星形胶质细胞上清液中Glu的摄取情况。结果 DA作用下原代培养星形胶质细胞中EAAT2表达显著降低,TAAR1水平升高。DA显著增强原代培养星形胶质细胞上清液中Glu的摄取。转染TAAR1 siRNA后,DA处理使EAAT2表达上调,上清液中Glu含量下调。相反,转染TAAR1质粒后,上清液中EAAT2表达下降,Glu水平升高。结论 DA通过TAAR1-EAAT2信号通路降低星形胶质细胞的Glu摄取能力,导致细胞外Glu蓄积,最终破坏星形胶质细胞功能。