Department of Biology, and.
Neuroscience Institute, Georgia State University, Atlanta, Georgia, 30303.
J Neurosci. 2019 Jan 23;39(4):596-611. doi: 10.1523/JNEUROSCI.1379-18.2018. Epub 2018 Nov 30.
Neurons operate within defined activity limits, and feedback control mechanisms dynamically tune ionic currents to maintain this optimal range. This study describes a novel, rapid feedback mechanism that uses SUMOylation to continuously adjust ionic current densities according to changes in activity. Small ubiquitin-like modifier (SUMO) is a peptide that can be post-translationally conjugated to ion channels to influence their surface expression and biophysical properties. Neuronal activity can regulate the extent of protein SUMOylation. This study on the single, unambiguously identifiable lateral pyloric neuron (LP), a component of the pyloric network in the stomatogastric nervous system of male and female spiny lobsters (), focused on dynamic SUMOylation in the context of activity homeostasis. There were four major findings: First, neuronal activity adjusted the balance between SUMO conjugation and deconjugation to continuously and bidirectionally fine-tune the densities of two opposing conductances: the hyperpolarization activated current (I) and the transient potassium current (I). Second, tonic 5 nm dopamine (DA) gated activity-dependent SUMOylation to permit and prevent activity-dependent regulation of I and I, respectively. Third, DA-gated, activity-dependent SUMOylation contributed to a feedback mechanism that restored the timing and duration of LP activity during prolonged modulation by 5 μm DA, which initially altered these and other activity features. Fourth, DA modulatory and metamoduatory (gating) effects were tailored to simultaneously alter and stabilize neuronal output. Our findings suggest that modulatory tone may select a subset of rapid activity-dependent mechanisms from a larger menu to achieve homeostasis under varying conditions. Post-translational SUMOylation of ion channel subunits controls their interactions. When subunit SUMOylation is dysregulated, conductance densities mediated by the channels are distorted, leading to nervous system disorders, such as seizures and chronic pain. Regulation of ion channel SUMOylation is poorly understood. This study demonstrated that neuronal activity can regulate SUMOylation to reconfigure ionic current densities over minutes, and this regulation was gated by tonic nanomolar dopamine. Dynamic SUMOylation was necessary to maintain specific aspects of neuronal output while the neuron was being modulated by high (5 μm) concentrations of dopamine, suggesting that the gating function may ensure neuronal homeostasis during extrinsic modulation of a circuit.
神经元在特定的活动范围内运作,反馈控制机制则通过动态调节离子电流来维持这一最佳范围。本研究描述了一种新的快速反馈机制,该机制利用 SUMO 化作用根据活动变化持续调整离子电流密度。小泛素样修饰物 (SUMO) 是一种可以被翻译后修饰的肽,可影响离子通道的表面表达和生物物理特性。神经元活动可以调节蛋白质 SUMO 化的程度。本研究针对单一、明确可识别的侧幽门神经元 (LP),这是雄性和雌性刺龙虾口胃神经系统中幽门网络的组成部分,重点研究了活性自稳过程中动态 SUMO 化的作用。主要有四个发现:首先,神经元活动调节 SUMO 结合和解离之间的平衡,持续双向微调两种相反电流的密度:超极化激活电流 (I) 和短暂钾电流 (I)。其次,持续的 5nm 多巴胺(DA)门控活性依赖 SUMO 化允许并防止 I 和 I 的活性依赖性调节。第三,DA 门控活性依赖 SUMO 化有助于反馈机制,该机制在长时间由 5μm DA 调制时恢复 LP 活动的时间和持续时间,最初改变这些和其他活动特征。第四,DA 调制和变调(门控)作用被调整为同时改变和稳定神经元输出。我们的研究结果表明,在不同条件下,调节音调可能会从更大的菜单中选择一组快速的活动依赖机制来实现自稳。离子通道亚基的翻译后 SUMO 化控制它们的相互作用。当亚基 SUMO 化失调时,通道介导的电导密度会发生扭曲,导致神经系统疾病,如癫痫发作和慢性疼痛。离子通道 SUMO 化的调节知之甚少。本研究表明,神经元活动可以在数分钟内调节 SUMO 化作用以重新配置离子电流密度,这种调节由持续的纳米摩尔多巴胺控制。动态 SUMO 化对于维持神经元在高浓度(5μm)多巴胺调制时的特定输出方面是必要的,这表明门控功能可能确保了神经元在电路的外部调制期间的自稳。