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哺乳动物视网膜中的固有和诱导性神经元再生。

Intrinsic and Induced Neuronal Regeneration in the Mammalian Retina.

机构信息

Department of Ophthalmology, Spencer Center for Vision Research, Byers Eye Institute, Stanford University, Palo Alto, California, USA.

出版信息

Antioxid Redox Signal. 2023 Dec;39(16-18):1039-1052. doi: 10.1089/ars.2023.0309. Epub 2023 Jul 31.

DOI:10.1089/ars.2023.0309
Abstract

Retinal neurons are vulnerable to disease and injury, which can result in neuronal death and degeneration leading to irreversible vision loss. The human retina does not regenerate to replace neurons lost to disease or injury. However, cells within the retina of other animals are capable of regenerating neurons, and homologous cells within the mammalian retina could potentially be prompted to do the same. Activating evolutionarily silenced intrinsic regenerative capacity of the mammalian retina could slow, or even reverse, vision loss, leading to an improved quality of life for millions of people. During development, neurons in the retina are generated progressively by retinal progenitor cells, with distinct neuron types born over developmental time. Many genes function in this process to specify the identity of newly generated neuron types, and these appropriate states of gene expression inform recent regenerative work. When regeneration is initiated in other vertebrates, including birds and fish, specific signaling pathways control the efficiency of regeneration, and these conserved pathways are likely to be important in mammals as well. Using insights from development and from other animals, limited regeneration from intrinsic cell types has been demonstrated in the mammalian retina, but it is able only to generate a subset of partially differentiated retinal neuron types. Future studies should aim at increasing the efficiency of regeneration, activating regeneration in a targeted fashion across the retina, and improving the ability to generate specific types of retinal neurons to replace those lost to disease or injury. . 39, 1039-1052.

摘要

视网膜神经元易受疾病和损伤的影响,这可能导致神经元死亡和变性,从而导致不可逆转的视力丧失。人类的视网膜不能再生以替代因疾病或损伤而丧失的神经元。然而,其他动物的视网膜内的细胞能够再生神经元,哺乳动物视网膜内的同源细胞也有可能被促使这样做。激活哺乳动物视网膜中进化上沉默的内在再生能力,可以减缓甚至逆转视力丧失,为数百万患者提高生活质量。 在发育过程中,视网膜中的神经元是由视网膜祖细胞逐渐产生的,不同的神经元类型在发育过程中产生。许多基因在这个过程中起作用,以确定新生成的神经元类型的身份,这些适当的基因表达状态为最近的再生工作提供了信息。当其他脊椎动物(包括鸟类和鱼类)开始再生时,特定的信号通路控制着再生的效率,这些保守的通路在哺乳动物中也可能很重要。 利用来自发育和其他动物的见解,已经在哺乳动物的视网膜中证明了内在细胞类型的有限再生,但它只能产生部分分化的视网膜神经元类型的子集。 未来的研究应该旨在提高再生的效率,有针对性地激活整个视网膜的再生,并提高生成特定类型的视网膜神经元的能力,以替代因疾病或损伤而丧失的神经元。. 39, 1039-1052.

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