斑马鱼小脑退行性疾病的遗传模型和神经元再生机制。

IF 6.2 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Cellular and Molecular Life Sciences Pub Date : 2024-12-27 DOI:10.1007/s00018-024-05538-z
Kazuhiko Namikawa, Sol Pose-Méndez, Reinhard W Köster
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引用次数: 0

摘要

小脑是脊椎动物中高度保守的脑区。人类小脑的遗传性疾病通常会导致主要神经元浦肯野细胞的退化,从而导致运动障碍和社会情感障碍。由于其相对简单但高度保守的神经解剖学和电路,这些人类疾病可以在适合基因操作的脊椎动物中很好地建模。近年来,对斑马鱼小脑的研究有助于了解小脑的发育和功能,因为斑马鱼幼虫不仅在分子上易于处理,而且由于幼虫的透明性和易于进入斑马鱼小脑皮层进行显微镜检查,因此可以进行高分辨率的体内成像。因此,斑马鱼越来越多地用于人类小脑神经退行性疾病的遗传建模,特别是不同类型的脊髓小脑共济失调(SCAs)。这些模型非常适合通过体内细胞生物学研究来解决潜在的致病机制。此外,伴随的电路表征、生理研究和行为分析允许解开分子、结构和功能关系。此外,与哺乳动物不同的是,斑马鱼具有惊人的再生神经元群和中枢神经系统(包括小脑)功能回路的能力。了解这些再生过程的细胞和分子过程可以很好地抵消人类神经元的急性和慢性损失。基于小脑的高度进化保护,这些在斑马鱼中的再生研究有望为对抗小脑神经元变性开辟治疗途径。本综述旨在概述目前存在的斑马鱼小脑神经退行性疾病的遗传模型以及利用斑马鱼小脑进行神经再生的研究。由于在小脑疾病建模和神经元再生分析方面的坚实基础,斑马鱼有望成为揭示人类小脑疾病致病机制和为治疗性神经元再生方法提供切入点的流行模式生物。
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Genetic modeling of degenerative diseases and mechanisms of neuronal regeneration in the zebrafish cerebellum.

The cerebellum is a highly conserved brain compartment of vertebrates. Genetic diseases of the human cerebellum often lead to degeneration of the principal neuron, the Purkinje cell, resulting in locomotive deficits and socio-emotional impairments. Due to its relatively simple but highly conserved neuroanatomy and circuitry, these human diseases can be modeled well in vertebrates amenable for genetic manipulation. In the recent years, cerebellar research in zebrafish has contributed to understanding cerebellum development and function, since zebrafish larvae are not only molecularly tractable, but also accessible for high resolution in vivo imaging due to the transparency of the larvae and the ease of access to the zebrafish cerebellar cortex for microscopy approaches. Therefore, zebrafish is increasingly used for genetic modeling of human cerebellar neurodegenerative diseases and in particular of different types of Spinocerebellar Ataxias (SCAs). These models are well suited to address the underlying pathogenic mechanisms by means of in vivo cell biological studies. Furthermore, accompanying circuitry characterizations, physiological studies and behavioral analysis allow for unraveling molecular, structural and functional relationships. Moreover, unlike in mammals, zebrafish possess an astonishing ability to regenerate neuronal populations and their functional circuitry in the central nervous system including the cerebellum. Understanding the cellular and molecular processes of these regenerative processes could well serve to counteract acute and chronic loss of neurons in humans. Based on the high evolutionary conservation of the cerebellum these regeneration studies in zebrafish promise to open therapeutic avenues for counteracting cerebellar neuronal degeneration. The current review aims to provide an overview over currently existing genetic models of human cerebellar neurodegenerative diseases in zebrafish as well as neuroregeneration studies using the zebrafish cerebellum. Due to this solid foundation in cerebellar disease modeling and neuronal regeneration analysis, the zebrafish promises to become a popular model organism for both unraveling pathogenic mechanisms of human cerebellar diseases and providing entry points for therapeutic neuronal regeneration approaches.

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来源期刊
Cellular and Molecular Life Sciences
Cellular and Molecular Life Sciences 生物-生化与分子生物学
CiteScore
13.20
自引率
1.20%
发文量
546
审稿时长
1.0 months
期刊介绍: Journal Name: Cellular and Molecular Life Sciences (CMLS) Location: Basel, Switzerland Focus: Multidisciplinary journal Publishes research articles, reviews, multi-author reviews, and visions & reflections articles Coverage: Latest aspects of biological and biomedical research Areas include: Biochemistry and molecular biology Cell biology Molecular and cellular aspects of biomedicine Neuroscience Pharmacology Immunology Additional Features: Welcomes comments on any article published in CMLS Accepts suggestions for topics to be covered
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