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Innervation of Gill Lateral Cells in the Bivalve Mollusc Crassostrea virginica Affects Cellular Membrane Potential and Cilia Activity. 双壳软体动物鳃侧细胞的神经支配影响细胞膜电位和纤毛活动
Pub Date : 2016-05-01 Epub Date: 2016-03-26
Edward J Catapane, Michael Nelson, Trevon Adams, Margaret A Carroll

Gill lateral cells of Crassostrea virginica are innervated by the branchial nerve, which contains serotonergic and dopaminergic fibers that regulate cilia beating rate. Terminal release of serotonin or dopamine results in an increase or decrease, respectively, of cilia beating rate in lateral gill cells. In this study we used the voltage sensitive fluorescent probe DiBAC4(3) to quantify changes in gill lateral cell membrane potential in response to electrical stimulation of the branchial nerve or to applications of serotonin and dopamine, and correlate these changes to cilia beating rates. Application of serotonin to gill lateral cells caused prolonged membrane depolarization, similar to plateau potentials, while increasing cilia beating rate. Application of dopamine hyperpolarized the resting membrane while decreasing cilia beating rate. Low frequency (5 Hz) electrical stimulations of the branchial nerve, which cause terminal release of endogenous serotonin, or high frequency (20 Hz) stimulations, which cause terminal release of endogenous dopamine, had the same effects on gill lateral cell membrane potentials and cilia beating rate as the respective applications of serotonin or dopamine. The study shows that innervation of gill lateral cells by the branchial nerve affects membrane potential as well as cilia beating rate, and demonstrates a strong correlation between changes in membrane potential and regulation of cilia beating rate. The study furthers the understanding of serotonin and dopamine signaling in the innervation and regulation of gill cilia in bivalves. The study also shows that voltage sensitive fluorescent probes like DiBAC 4(3) can be successfully used as an alternative to microelectrodes to measure changes in membrane potential of ciliated gill cells and other small cells with fast moving cilia.

弗氏鲫的鳃侧细胞受支气管神经支配,支气管神经中含有能调节纤毛跳动率的血清素能纤维和多巴胺能纤维。5-羟色胺或多巴胺的终端释放分别导致侧鳃细胞纤毛跳动率的增加或减少。在这项研究中,我们使用电压敏感的荧光探针 DiBAC4(3) 来量化鳃侧细胞膜电位在支神经电刺激或应用羟色胺和多巴胺时的变化,并将这些变化与纤毛跳动率联系起来。对鳃侧细胞施用血清素会导致膜去极化延长,类似于高原电位,同时增加纤毛的跳动率。应用多巴胺可使静息膜超极化,同时降低纤毛跳动率。低频(5 Hz)电刺激支气管神经会导致内源性血清素的末端释放,高频(20 Hz)刺激支气管神经会导致内源性多巴胺的末端释放,这两种刺激对鳃侧细胞膜电位和纤毛跳动率的影响与应用血清素或多巴胺的影响相同。该研究表明,支神经对鳃侧细胞的支配会影响膜电位和纤毛的跳动率,并证明膜电位的变化与纤毛跳动率的调节之间存在很强的相关性。该研究进一步加深了人们对双壳类动物鳃纤毛神经支配和调节过程中血清素和多巴胺信号传导的理解。该研究还表明,电压敏感荧光探针(如 DiBAC 4(3))可成功替代微电极,用于测量纤毛鳃细胞和其他具有快速运动纤毛的小细胞的膜电位变化。
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Journal of pharmacological reports
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