Cheng Pi-Cheng, Chen Ya-Shuan, Huang Rong-Chi
Department of Physiology and Pharmacology, College of Medicine, Chang Gung University, Tao-Yuan 33305, Taiwan, Republic of China.
Healthy Aging Research Center, Chang Gung University, Tao-Yuan 33305, Taiwan, Republic of China.
Chin J Physiol. 2017 Aug 31;60(4):215-225. doi: 10.4077/CJP.2017.BAF480.
The plasmalemmal Na⁺/Ca²⁺ changer (NCX) regulates intracellular Ca²⁺ by exchanging 3 Na⁺ for 1 Ca²⁺ in either the Ca²⁺ exit or Ca²⁺ entry mode. All three NCX isoforms NCX1, NCX2, and NCX3 are expressed in the rat brain, with isoform-specific differential distribution. In the central clock of suprachiasmatic nucleus (SCN), intracellular Ca²⁺ controls the circadian release of major neuropeptides, which are the arginine vasopressin (AVP), vasoactive intestinal peptide (VIP) and gastrin releasing peptide (GRP), and the NCX, most likely NCX1, rapidly clears depolarization-induced somatic Ca²⁺ influx. However, the role of NCX2 in the SCN remains unknown. This study aimed to investigate the colocalization of NCX2 with neuropeptides and daily expression profiles of NCX2 in mRNA and protein levels. Consistent with the restricted distribution of NCX2 in the retinorecipient ventral SCN, the immunostaining results showed colocalization of NCX2 with VIP, GRP and VIP/GRP in the ventral SCN, but not with AVP in the dorsal SCN, or markers for astrocyte and major input pathways. Importantly, the presynaptic marker Bassoon was found to colocalize with NCX2/GRP and NCX2/ VIP, indicating localization of both VIP/NCX2 and GRP/NCX2 at the presynaptic sites. Furthermore, real-time PCR and western blotting revealed no day-night difference in NCX2 mRNA and protein levels, in contrast to a robust circadian rhythm in the expression of clock genes Per1 and Per2. Together the results suggest a role of NCX2 in the regulation of the release of VIP and GRP.
质膜钠钙交换体(NCX)通过在钙外流或钙内流模式下用3个钠离子交换1个钙离子来调节细胞内钙离子浓度。NCX的三种亚型NCX1、NCX2和NCX3均在大鼠脑中表达,且具有亚型特异性的差异分布。在视交叉上核(SCN)的中央生物钟中,细胞内钙离子控制着主要神经肽的昼夜释放,这些神经肽包括精氨酸加压素(AVP)、血管活性肠肽(VIP)和胃泌素释放肽(GRP),而NCX(很可能是NCX1)能迅速清除去极化诱导的体细胞钙离子内流。然而,NCX2在SCN中的作用尚不清楚。本研究旨在探究NCX2与神经肽的共定位情况以及NCX2在mRNA和蛋白质水平的每日表达谱。与NCX2在接受视网膜投射的腹侧SCN中的局限性分布一致,免疫染色结果显示腹侧SCN中NCX2与VIP、GRP以及VIP/GRP共定位,但在背侧SCN中不与AVP共定位,也不与星形胶质细胞和主要输入通路的标志物共定位。重要的是,发现突触前标志物巴松管与NCX2/GRP和NCX2/VIP共定位,表明VIP/NCX2和GRP/NCX2均定位于突触前位点。此外,实时PCR和蛋白质印迹分析显示,与生物钟基因Per1和Per2表达的强烈昼夜节律不同,NCX2的mRNA和蛋白质水平没有昼夜差异。这些结果共同表明NCX2在调节VIP和GRP释放中发挥作用。