CaMK4, a key target for treating pathogenesis of depression?

IF 5.6 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Yang Yang, Wei Guan, Hai-Juan Gu
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引用次数: 0

Abstract

Depression is a common clinical mental disorder characterized by persistent low mood and anhedonia. Although there is strong evidence indicating that chronic stress is a major contributor to the pathogenesis of depression, its precise mechanisms and physiological effects remain unclear. Calcium/calmodulin-dependent protein kinase IV (CaMK4) is a multifunctional serine/threonine kinase that is predominantly expressed in various cell types, including lymphocytes, nerve cells, and thymocytes, and it is a crucial mediator in the regulation of gene expression through the activation of various transcription factors. It regulates cellular signaling pathways by phosphorylating downstream target proteins and is closely associated with the occurrence and development of various diseases. In recent years, an increasing number of studies have shown that CaMK4 is a core component of the Ca2+-calmodulin-activated signaling pathway and plays a crucial role in regulating neural development and synaptic plasticity, while impairments in these aspects are all associated with depression. Nevertheless, the exact molecular involvement of CaMK4 in the development of depression has not been determined. In this review, we summarize evidence that suggests CaMK4 plays an important role in the occurrence and development of depression. We also discuss the consequences of the dysregulation of CaMK4 signalling transduction in this disease, emphasizing its impact on hippocampal neurogenesis and synaptic plasticity. It is hoped that a comprehensive understanding of the role of CaMK4 in the pathogenesis of depression will provide knowledge to assist the development of new antidepressant drugs.

CaMK4是治疗抑郁症发病机制的关键靶点?
抑郁症是一种常见的临床精神障碍,其特征是持续的情绪低落和快感缺乏。尽管有强有力的证据表明慢性压力是抑郁症发病机制的主要因素,但其确切机制和生理影响尚不清楚。钙/钙调素依赖性蛋白激酶IV (CaMK4)是一种多功能丝氨酸/苏氨酸激酶,主要表达于各种细胞类型,包括淋巴细胞、神经细胞和胸腺细胞,它是通过激活各种转录因子调节基因表达的重要介质。它通过磷酸化下游靶蛋白调控细胞信号通路,与多种疾病的发生发展密切相关。近年来,越来越多的研究表明,CaMK4是Ca2+-钙调素激活信号通路的核心组分,在调节神经发育和突触可塑性方面起着至关重要的作用,而这些方面的损伤都与抑郁症有关。然而,CaMK4在抑郁症发展中的确切分子参与尚未确定。在这篇综述中,我们总结了表明CaMK4在抑郁症的发生和发展中起重要作用的证据。我们还讨论了CaMK4信号转导失调在这种疾病中的后果,强调其对海马神经发生和突触可塑性的影响。希望全面了解CaMK4在抑郁症发病机制中的作用,为开发新的抗抑郁药物提供知识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biochemical pharmacology
Biochemical pharmacology 医学-药学
CiteScore
10.30
自引率
1.70%
发文量
420
审稿时长
17 days
期刊介绍: Biochemical Pharmacology publishes original research findings, Commentaries and review articles related to the elucidation of cellular and tissue function(s) at the biochemical and molecular levels, the modification of cellular phenotype(s) by genetic, transcriptional/translational or drug/compound-induced modifications, as well as the pharmacodynamics and pharmacokinetics of xenobiotics and drugs, the latter including both small molecules and biologics. The journal''s target audience includes scientists engaged in the identification and study of the mechanisms of action of xenobiotics, biologics and drugs and in the drug discovery and development process. All areas of cellular biology and cellular, tissue/organ and whole animal pharmacology fall within the scope of the journal. Drug classes covered include anti-infectives, anti-inflammatory agents, chemotherapeutics, cardiovascular, endocrinological, immunological, metabolic, neurological and psychiatric drugs, as well as research on drug metabolism and kinetics. While medicinal chemistry is a topic of complimentary interest, manuscripts in this area must contain sufficient biological data to characterize pharmacologically the compounds reported. Submissions describing work focused predominately on chemical synthesis and molecular modeling will not be considered for review. While particular emphasis is placed on reporting the results of molecular and biochemical studies, research involving the use of tissue and animal models of human pathophysiology and toxicology is of interest to the extent that it helps define drug mechanisms of action, safety and efficacy.
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