KCC2治疗神经系统疾病的进展。

IF 3.5 3区 医学 Q2 NEUROSCIENCES Frontiers in Molecular Neuroscience Pub Date : 2024-12-10 eCollection Date: 2024-01-01 DOI:10.3389/fnmol.2024.1503070
Shilpa D Kadam, Shane V Hegarty
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引用次数: 0

摘要

KCC2是中枢神经系统神经元特异性氯离子挤出剂,对跨膜氯离子梯度的建立和维持至关重要,从而实现中枢神经系统内的突触抑制。在此,我们强调KCC2功能障碍是导致神经元回路兴奋/抑制(E/I)失衡的一种基本和保守的病理,这种失衡是癫痫、慢性疼痛、神经发育/创伤/退行性/精神疾病的基础。事实上,在后天和遗传因素的下游,多种病理(如高兴奋性和炎症)汇聚在一起,损害了中枢神经系统中kcc2依赖性抑制。当KCC2功能低下时,受影响的神经元由于对GABA/甘氨酸的抑制反应受损而被去抑制。这会导致神经元的高兴奋性、神经元回路的去抑制和神经功能的破坏。最近,KCC2被确定为癫痫、智力残疾和自闭症谱系障碍的基因验证靶点,人类SLC12A5基因的致病性突变与精神/情绪障碍有关。kcc2上调药物的广泛治疗用途与它在确定gaba能神经传递抑制活性方面的关键作用有关,这是多种药物广泛靶向的机制。然而,在KCC2功能低下的情况下,gabaergy神经传递可能是去极化/兴奋性的,从而损害内源性神经元抑制,同时也限制了现有靶向/需要gabaergy通路抑制的治疗方法的有效性。一些临床前报告表明,KCC2上调治疗可以挽救和增加抗癫痫和镇痛药物的疗效。因此,一流的kcc2增强疗法将为恢复生理性CNS抑制和解决E/I失衡病理患者的耐药性提供新机制。在此,我们讨论了开发一流的KCC2治疗方法来治疗神经系统疾病患者的进展和进一步的工作。
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Development of KCC2 therapeutics to treat neurological disorders.

KCC2 is CNS neuron-specific chloride extruder, essential for the establishment and maintenance of the transmembrane chloride gradient, thereby enabling synaptic inhibition within the CNS. Herein, we highlight KCC2 hypofunction as a fundamental and conserved pathology contributing to neuronal circuit excitation/inhibition (E/I) imbalances that underly epilepsies, chronic pain, neuro-developmental/-traumatic/-degenerative/-psychiatric disorders. Indeed, downstream of both acquired and genetic factors, multiple pathologies (e.g., hyperexcitability and inflammation) converge to impair KCC2-dependent inhibition in CNS. When KCC2 hypofunction occurs, affected neurons are disinhibited due to impaired inhibitory responses to GABA/glycine. This causes neuronal hyperexcitability, disinhibition within neuron circuits, and disrupted neurological functions. More recently, KCC2 was identified as a genetically-validated target for epilepsy, intellectual disability, and autism spectrum disorder, and pathogenic mutations in human SLC12A5 gene were linked to psychiatric/mood disorders. The broad therapeutic utility of KCC2-upmodulating drugs relates to its critical role in determining inhibitory activity of GABAergic neurotransmission, a mechanism widely targeted by several drugs. However, in cases of KCC2 hypofunction GABAergic neurotransmission can be depolarizing/excitatory, thereby impairing endogenous neuronal inhibition while also limiting the effectiveness of existing therapeutics targeting/requiring GABAergic pathway inhibition. Several preclinical reports have shown that KCC2 upmodulating treatments rescue and increase the efficacy of anti-seizure and analgesic medications. Thus, a first-in-class KCC2-potentiating therapy would provide a novel mechanism for restoring physiological CNS inhibition and addressing drug resistance in patients with E/I imbalance pathologies. Herein, we discuss progress toward and further work needed to develop the first-in-class KCC2 therapeutics to treat neurological disorder patients.

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来源期刊
CiteScore
5.70
自引率
2.10%
发文量
669
审稿时长
14 weeks
期刊介绍: Frontiers in Molecular Neuroscience is a first-tier electronic journal devoted to identifying key molecules, as well as their functions and interactions, that underlie the structure, design and function of the brain across all levels. The scope of our journal encompasses synaptic and cellular proteins, coding and non-coding RNA, and molecular mechanisms regulating cellular and dendritic RNA translation. In recent years, a plethora of new cellular and synaptic players have been identified from reduced systems, such as neuronal cultures, but the relevance of these molecules in terms of cellular and synaptic function and plasticity in the living brain and its circuits has not been validated. The effects of spine growth and density observed using gene products identified from in vitro work are frequently not reproduced in vivo. Our journal is particularly interested in studies on genetically engineered model organisms (C. elegans, Drosophila, mouse), in which alterations in key molecules underlying cellular and synaptic function and plasticity produce defined anatomical, physiological and behavioral changes. In the mouse, genetic alterations limited to particular neural circuits (olfactory bulb, motor cortex, cortical layers, hippocampal subfields, cerebellum), preferably regulated in time and on demand, are of special interest, as they sidestep potential compensatory developmental effects.
期刊最新文献
Uncovering novel KCC2 regulatory motifs through a comprehensive transposon-based mutant library. Novel strategies targeting mitochondria-lysosome contact sites for the treatment of neurological diseases. Editorial: Oxytosis/ferroptosis: unraveling the mechanisms and its multifaceted role in neurodegenerative diseases. Neurotherapeutic impact of vanillic acid and ibudilast on the cuprizone model of multiple sclerosis. Serum metabolomic signatures of patients with rare neurogenetic diseases: an insight into potential biomarkers and treatment targets.
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