Sgobio Carmelo, Kupferschmidt David A, Cui Guohong, Sun Lixin, Li Zheng, Cai Huaibin, Lovinger David M
Transgenics Section, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, United States of America.
Laboratory of Integrative Neuroscience, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Rockville, Maryland, United States of America.
PLoS One. 2014 Oct 31;9(10):e111749. doi: 10.1371/journal.pone.0111749. eCollection 2014.
Calcium triggers dopamine release from presynaptic terminals of midbrain dopaminergic (mDA) neurons in the striatum. However, calcium transients within mDA axons and axon terminals are difficult to study and little is known about how they are regulated. Here we use a newly-developed method to measure presynaptic calcium transients (PreCaTs) in axons and terminals of mDA neurons with a genetically encoded calcium indicator (GECI) GCaMP3 expressed in transgenic mice. Using a photomultiplier tube-based system, we measured electrical stimulation-induced PreCaTs of mDA neurons in dorsolateral striatum slices from these mice. Single-pulse stimulation produced a transient increase in fluorescence that was completely blocked by a combination of N- and P/Q-type calcium channel blockers. DA and cholinergic, but not serotoninergic, signaling pathways modulated the PreCaTs in mDA fibers. These findings reveal heretofore unexplored dynamic modulation of presynaptic calcium in nigrostriatal terminals.
钙触发中脑多巴胺能(mDA)神经元的突触前终末向纹状体释放多巴胺。然而,mDA轴突和轴突终末内的钙瞬变很难研究,对于它们如何被调节也知之甚少。在此,我们使用一种新开发的方法,利用在转基因小鼠中表达的基因编码钙指示剂(GECI)GCaMP3来测量mDA神经元轴突和终末中的突触前钙瞬变(PreCaTs)。使用基于光电倍增管的系统,我们测量了这些小鼠背外侧纹状体切片中电刺激诱导的mDA神经元的PreCaTs。单脉冲刺激使荧光短暂增加,这被N型和P/Q型钙通道阻滞剂的组合完全阻断。多巴胺能和胆碱能信号通路而非5-羟色胺能信号通路调节了mDA纤维中的PreCaTs。这些发现揭示了黑质纹状体终末中突触前钙迄今未被探索的动态调节。