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健康与疾病中离子通道的SUMO调节

SUMO Regulation of Ion Channels in Health and Disease.

作者信息

Connolly Jenna G, Plant Leigh D

机构信息

Department of Pharmaceutical Sciences and the Center for Drug Discovery, The School of Pharmacy and Pharmaceutical SciencesBouvé College of Health Sciences, Northeastern University, Boston, Massachusetts, United States.

出版信息

Physiology (Bethesda). 2025 Mar 1;40(2):0. doi: 10.1152/physiol.00034.2024. Epub 2024 Nov 5.

DOI:10.1152/physiol.00034.2024
PMID:39499247
Abstract

The small ubiquitin-like modifier (SUMO) protein pathway governs a panoply of vital biological processes including cell death, proliferation, differentiation, metabolism, and signal transduction by diversifying the functions, half-lives, and partnerships of target proteins in situ. More recently, SUMOylation has emerged as a key regulator of ion homeostasis and excitability across multiple tissues due to the regulation of a plethora of ion channels expressed in a range of tissue subtypes. Altogether, the balance of SUMOylation states among relevant ion channels can result in graded biophysical effects that tune excitability and contribute to a range of disease states including cardiac arrhythmia, epilepsy, pain transmission, and inflammation. Here, we consolidate these concepts by focusing on the role of ion channel SUMOylation in the central nervous system, peripheral nervous system, and cardiovascular system. In addition, we review what is known about the enigmatic factors that regulate the SUMO pathway and consider the emerging role of small molecule SUMO modulators as potential therapeutics in a range of diseases.

摘要

小泛素样修饰物(SUMO)蛋白途径通过在原位使靶蛋白的功能、半衰期和伙伴关系多样化,从而掌控着一系列重要的生物学过程,包括细胞死亡、增殖、分化、代谢和信号转导。最近,由于对一系列组织亚型中表达的众多离子通道的调节,SUMO化已成为多种组织中离子稳态和兴奋性的关键调节因子。总之,相关离子通道之间SUMO化状态的平衡可导致分级生物物理效应,从而调节兴奋性,并导致包括心律失常、癫痫、疼痛传递和炎症在内的一系列疾病状态。在这里,我们通过关注离子通道SUMO化在中枢神经系统、外周神经系统和心血管系统中的作用来整合这些概念。此外,我们回顾了已知的调节SUMO途径的神秘因素,并考虑小分子SUMO调节剂作为一系列疾病潜在治疗药物的新兴作用。

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本文引用的文献

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Mechanistic basis of the dynamic response of TWIK1 ionic selectivity to pH.TWIK1离子选择性对pH动态响应的机制基础。
Nat Commun. 2024 May 8;15(1):3849. doi: 10.1038/s41467-024-48067-w.
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The Concise Guide to PHARMACOLOGY 2023/24: Ion channels.《药理学简明指南 2023/24 年版》:离子通道。
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hnRNPA1 SUMOylation promotes cold hypersensitivity in chronic inflammatory pain by stabilizing TRPA1 mRNA.hnRNPA1 SUMOylation 通过稳定 TRPA1 mRNA 促进慢性炎症性疼痛中的冷敏性。
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Targeted transcriptional upregulation of SENP1 by CRISPR activation enhances deSUMOylation pathways to elicit antinociception in the spinal nerve ligation model of neuropathic pain.通过 CRISPR 激活靶向转录上调 SENP1,增强去 SUMOylation 途径,在神经病理性疼痛的脊神经结扎模型中产生镇痛作用。
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Intranasal CRMP2-Ubc9 inhibitor regulates Na V 1.7 to alleviate trigeminal neuropathic pain.鼻内 CRMP2-Ubc9 抑制剂调节 NaV1.7 缓解三叉神经病理性疼痛。
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SUMOylation of the cardiac sodium channel Na1.5 modifies inward current and cardiac excitability.SUMOylation 修饰心脏钠离子通道 Na1.5 可改变内向电流和心脏兴奋性。
Heart Rhythm. 2023 Nov;20(11):1548-1557. doi: 10.1016/j.hrthm.2023.07.067. Epub 2023 Aug 3.
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Trackable Intratumor Microdosing and Spatial Profiling Provide Early Insights into Activity of Investigational Agents in the Intact Tumor Microenvironment.可追踪的肿瘤内微量投药和空间分析为深入了解在完整肿瘤微环境中研究药物的活性提供了早期见解。
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SUMOylation of Na1.2 channels regulates the velocity of backpropagating action potentials in cortical pyramidal neurons.SUMOylation 修饰调控皮质锥体神经元中逆行动作电位的传播速度。
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9
Hypoxia inhibits the cardiac current through SUMO targeting Kir2.1 activation by PIP.缺氧通过小泛素样修饰蛋白(SUMO)靶向磷脂酰肌醇磷酸(PIP)激活内向整流钾通道2.1(Kir2.1)来抑制心脏电流。
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TRPV1 SUMOylation suppresses itch by inhibiting TRPV1 interaction with H1 receptors.TRPV1 SUMOylation 通过抑制 TRPV1 与 H1 受体的相互作用来抑制瘙痒。
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