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Akt介导的抗抑郁药敏感性5-羟色胺转运体功能、细胞表面表达及磷酸化的调控

Akt-mediated regulation of antidepressant-sensitive serotonin transporter function, cell-surface expression and phosphorylation.

作者信息

Rajamanickam Jeyaganesh, Annamalai Balasubramaniam, Rahbek-Clemmensen Troels, Sundaramurthy Santhanalakshmi, Gether Ulrik, Jayanthi Lankupalle D, Ramamoorthy Sammanda

机构信息

*Department of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond, VA 23298, U.S.A.

†Department of Neurosciences, Medical University of South Carolina, Charleston, SC 29425, U.S.A.

出版信息

Biochem J. 2015 May 15;468(1):177-90. doi: 10.1042/BJ20140826.

Abstract

The serotonin [5-HT (5-hydroxytryptamine)] transporter (SERT) controls serotonergic neurotransmission in the brain by rapid clearance of 5-HT from the synaptic cleft into presynaptic neurons. SERTs are primary targets for antidepressants for therapeutic intervention of mood disorders. Our previous studies have identified the involvement of several signalling pathways and protein kinases in regulating SERT function, trafficking and phosphorylation. However, whether Akt/PKB (protein kinase) regulates SERT function is not known. In the present study, we made the novel observation that inhibition of Akt resulted in the down-regulation of SERT function through the regulation of SERT trafficking and phosphorylation. Akt inhibitor Akt X {10-(4'-[N-diethylamino)butyl]-2-chlorophenoxazine} reduced the endogenously phosphorylated Akt and significantly decreased 5-HT uptake and 5-HT-uptake capacity. Furthermore, SERT activity is also reduced by siRNA down-regulation of total and phospho-Akt levels. The reduction in SERT activity is paralleled by lower levels of cell-surface SERT protein, reduced SERT exocytosis with no effect on SERT endocytosis and accumulation of SERT in intracellular endocytic compartments with the most prominent localization to late endosomes and lysosomes. Akt2 inhibitor was more effective than Akt1 inhibitor in inhibiting SERT activity. Inhibition of downstream Akt kinase GSK3α/β (glycogen synthase kinase α/β) stimulates SERT function. Akt inhibition leads to a decrease in SERT basal phosphorylation. Our results provide evidence that Akt regulates SERT function and cell-surface expression by regulating the intracellular SERT distribution and plasma membrane availability, which perhaps may be linked to SERT phosphorylation state. Thus any changes in the activation of Akt and/or GSK3α/β could alter SERT-mediated 5-HT clearance and subsequently serotonergic neurotransmission.

摘要

血清素[5-羟色胺(5-HT)]转运体(SERT)通过将5-HT从突触间隙快速清除到突触前神经元中,来控制大脑中的血清素能神经传递。SERT是用于治疗情绪障碍的抗抑郁药的主要作用靶点。我们之前的研究已经确定了几种信号通路和蛋白激酶参与调节SERT的功能、转运和磷酸化。然而,Akt/蛋白激酶B(PKB)是否调节SERT功能尚不清楚。在本研究中,我们有了新的发现,即抑制Akt会通过调节SERT的转运和磷酸化导致SERT功能下调。Akt抑制剂Akt X {10-(4'-[N-二乙氨基)丁基]-2-氯吩恶嗪}降低了内源性磷酸化Akt,并显著降低了5-HT摄取和5-HT摄取能力。此外,通过小干扰RNA下调总Akt水平和磷酸化Akt水平,SERT活性也会降低。SERT活性的降低与细胞表面SERT蛋白水平降低、SERT胞吐作用减少平行,对SERT内吞作用无影响,且SERT在细胞内吞小室中积累,最显著地定位于晚期内体和溶酶体。Akt2抑制剂在抑制SERT活性方面比Akt1抑制剂更有效。抑制下游Akt激酶糖原合酶激酶α/β(GSK3α/β)可刺激SERT功能。Akt抑制导致SERT基础磷酸化减少。我们的结果提供了证据,表明Akt通过调节细胞内SERT分布和质膜可用性来调节SERT功能和细胞表面表达,这可能与SERT磷酸化状态有关。因此,Akt和/或GSK3α/β激活的任何变化都可能改变SERT介导的5-HT清除,进而改变血清素能神经传递。

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