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How voltage-gated calcium channels gate forms of homeostatic synaptic plasticity

机译:电压门控钙如何引导稳态突触可塑性的门型

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摘要

Throughout life, animals face a variety of challenges such as developmental growth, the presence of toxins, or changes in temperature. Neuronal circuits and synapses respond to challenges by executing an array of neuroplasticity paradigms. Some paradigms allow neurons to up- or downregulate activity outputs, while countervailing ones ensure that outputs remain within appropriate physiological ranges. A growing body of evidence suggests that homeostatic synaptic plasticity (HSP) is critical in the latter case. Voltage-gated calcium channels gate forms of HSP. Presynaptically, the aggregate data show that when synapse activity is weakened, homeostatic signaling systems can act to correct impairments, in part by increasing calcium influx through presynaptic CaV2-type channels. Increased calcium influx is often accompanied by parallel increases in the size of active zones and the size of the readily releasable pool of presynaptic vesicles. These changes coincide with homeostatic enhancements of neurotransmitter release. Postsynaptically, there is a great deal of evidence that reduced network activity and loss of calcium influx through CaV1-type calcium channels also results in adaptive homeostatic signaling. Some adaptations drive presynaptic enhancements of vesicle pool size and turnover rate via retrograde signaling, as well as de novo insertion of postsynaptic neurotransmitter receptors. Enhanced calcium influx through CaV1 after network activation or single cell stimulation can elicit the opposite response—homeostatic depression via removal of excitatory receptors. There exist intriguing links between HSP and calcium channelopathies—such as forms of epilepsy, migraine, ataxia, and myasthenia. The episodic nature of some of these disorders suggests alternating periods of stable and unstable function. Uncovering information about how calcium channels are regulated in the context of HSP could be relevant toward understanding these and other disorders.
机译:在整个生命过程中,动物都面临各种挑战,例如发育生长,毒素的存在或温度的变化。神经回路和突触通过执行一系列神经可塑性范例来应对挑战。一些范例允许神经元上调或下调活动输出,而相反的范例则确保输出保持在适当的生理范围内。越来越多的证据表明,在后一种情况下,稳态突触可塑性(HSP)至关重要。电压门控钙通道可以形成HSP的门。突触前,汇总数据显示,当突触活性减弱时,体内稳态信号传导系统可通过部分增加通过突触前CaV2型通道的钙流入来纠正损伤。钙流入的增加通常伴随着活性区的大小和突触前囊泡易于释放池的大小的平行增加。这些变化与神经递质释放的稳态增加相吻合。突触后,有大量证据表明,网络活动的减少和通过CaV1型钙通道引起的钙内流损失也导致了适应性稳态信号的产生。一些适应通过逆行信号以及突触后神经递质受体的重新插入来驱动突触前囊泡池大小和周转率的增强。网络激活或单细胞刺激后,通过CaV1增强的钙内流可以引起相反的反应-通过去除兴奋性受体来抑制体内稳态。 HSP与钙离子通道病之间存在有趣的联系,例如癫痫,偏头痛,共济失调和肌无力的形式。这些疾病中某些疾病的发作性暗示了稳定和不稳定功能的交替时期。揭示有关在HSP背景下如何调节钙通道的信息可能与了解这些疾病和其他疾病有关。

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