The Role of Neurogenesis in Brain Disorders

Bryan W. Luikart
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引用次数: 3

Abstract

Embryonic and post-natal neurogenesis are necessary for the organization of neuronal connectivity and activity that underly all behaviors. It therefore is not surprising that mutations in genes or environmental insults that alter neurogenesis cause an abundance of neurological and psychiatric disorders. In this special issue of Brain Plasticity we have gathered review articles that focus on, The Role of Neurogenesis in Brain Disorders. In this issue authors discuss the function of neurogenesis in development and post development. Additionally, there is a focus on behavioral impact of post-natal neurogenesis and how insults to this system directly contributed to neuropsychiatric disorders. Finally, some articles highlight disorders where alteration of postnatal neurogenesis is not the sole, or even major, contributing factor to disease pathogenesis, yet can be used as a powerful system to study cellular changes that are generalizable across brain regions. A basic understanding of the molecular mechanisms leading to embryonic cortical development has led to increased understanding of how mutations in genes contributing to this process contribute to diseases ranging from holoprosencephaly, developmental delay, epilepsy, and intellectual disability, to name a few. In the first article of this special issue Yabut and Pleasure review the process of embryonic neurogenesis. Specifically, they focus on the development of cortical projections neurons and the role of Sonic Hedgehog signaling in this process. Not only does this allow for an increased understanding of many neurodevelopmental disorders, it also uncovers pharmacological targets that may be leveraged to develop therapies. The emerging field studying the interrelationship of vascular and neuronal development holds promise for understanding birth-related brain injuries such as neonatal hypoxic-ischemic encephalopathy and adult disorders such as diabetes, hypertension, and Alzheimer’s disease. The article from Kirschen et al. reviews aspects of both perinatal and adult neurogenesis. They focus on the basic science of how regulation of vascular development and function impacts neurogenesis. Such work will lead to new strategies to decrease damage and increase regeneration in response to metabolic injury in the brain. For some disorders including depression, anxiety, and addiction alteration of hippocampal neurogenesis may directly contribute to the pathophysiology of disease. Hollos et al, review the well-studied link between adult neurogenesis, depression, and anxiety. Regulation of JNK directly in newborn granule neurons alters anxiety and depression related behaviors. Takashima and Mandyam review the link of neurogenesis to addiction with a focus on methamphetamine. They discuss that neurogenesis may lead to alteration of hippocampal plasticity underlying methamphetamine relapse. Both articles discuss new drugs and drug targets that modulate neurogenesis and produce therapeutic gains in the respective disorders. Hippocampal neurogenesis is exquisitely sensitive to alterations in neuronal activity. Danzer discusses how pathological activity, in the form of seizures, results in aberrant neurogenesis and development of newborn neurons with distinct morphological features. These abnormalities lead to alterations in circuit connectivity that favor further epileptogenesis. In support of this, Danzer discusses how mutations in genes such as Pten directly cause similar pathological changes in neurogenesis contributing to epilepsy. Thus, targeting neurogenesis directly is a promising treatment avenue for temporal lobe epilepsy.
神经发生在脑部疾病中的作用
胚胎和出生后的神经发生是所有行为基础下的神经元连接和活动组织所必需的。因此,改变神经发生的基因突变或环境损害导致大量神经和精神疾病也就不足为奇了。在这一期的《大脑可塑性》特刊中,我们收集了关于神经发生在脑部疾病中的作用的综述文章。本文讨论了神经发生在发育和发育后的功能。此外,还有一个重点是出生后神经发生的行为影响,以及对该系统的损害如何直接导致神经精神疾病。最后,一些文章强调,出生后神经发生的改变并不是疾病发病的唯一或主要因素,但可以作为一个强大的系统来研究整个大脑区域的细胞变化。对导致胚胎皮质发育的分子机制的基本了解,增加了对参与这一过程的基因突变如何导致从前脑畸形、发育迟缓、癫痫和智力残疾等疾病的理解。在本期特刊的第一篇文章中,Yabut和Pleasure回顾了胚胎神经发生的过程。具体来说,他们关注皮质投射神经元的发育以及Sonic Hedgehog信号在这一过程中的作用。这不仅使人们对许多神经发育障碍有了更多的了解,而且还发现了可能用于开发治疗方法的药理学靶点。研究血管和神经元发育相互关系的新兴领域有望理解与出生相关的脑损伤,如新生儿缺氧缺血性脑病和成人疾病,如糖尿病、高血压和阿尔茨海默病。Kirschen等人的文章回顾了围产期和成人神经发生的各个方面。他们专注于血管发育和功能的调节如何影响神经发生的基础科学。这项工作将导致新的策略,以减少损伤和增加再生,以应对大脑代谢损伤。对于一些疾病,包括抑郁、焦虑和成瘾,海马神经发生的改变可能直接参与疾病的病理生理。Hollos等人回顾了成人神经发生、抑郁和焦虑之间的联系。JNK在新生儿颗粒神经元中的直接调控改变了焦虑和抑郁相关的行为。Takashima和Mandyam回顾了神经发生与成瘾的联系,重点是甲基苯丙胺。他们讨论了神经发生可能导致海马可塑性的改变,这是甲基苯丙胺复发的基础。两篇文章都讨论了调节神经发生的新药和药物靶点,并在各自的疾病中产生治疗效果。海马神经发生对神经元活动的改变非常敏感。Danzer讨论了以癫痫发作形式的病理活动如何导致异常的神经发生和具有不同形态特征的新生神经元的发育。这些异常导致回路连接的改变,有利于进一步的癫痫发生。为了支持这一点,Danzer讨论了Pten等基因的突变如何直接导致神经发生中类似的病理变化,从而导致癫痫。因此,直接靶向神经发生治疗颞叶癫痫是一种很有前景的治疗途径。
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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