Muller Glia-Mediated Retinal Regeneration

被引:50
作者
Gao, Hui [1 ,2 ]
Luodan, A. [1 ,2 ]
Huang, Xiaona [1 ,2 ]
Chen, Xi [3 ]
Xu, Haiwei [1 ,2 ]
机构
[1] Third Mil Med Univ, Army Med Univ, Southwest Eye Hosp, Southwest Hosp, Chongqing 400038, Peoples R China
[2] Key Lab Visual Damage & Regenerat & Restorat Chon, Chongqing 400038, Peoples R China
[3] Capital Med Univ, Beijing Friendship Hosp, Dept Ophthalmol, Beijing 100050, Peoples R China
基金
中国国家自然科学基金;
关键词
Muller glia reprogramming; Retinal regeneration; Mechanisms; Advanced progress; CILIARY NEUROTROPHIC FACTOR; PROGENITOR CELLS; STEM-CELLS; NEURAL REGENERATION; SONIC HEDGEHOG; SIGNALING PATHWAY; ZEBRAFISH RETINA; GLUCOCORTICOID-RECEPTORS; NEURONAL PROGENITORS; HOST PHOTORECEPTORS;
D O I
10.1007/s12035-020-02274-w
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Muller glia originate from neuroepithelium and are the principal glial cells in the retina. During retinal development, Muller glia are one of the last cell types to be born. In lower vertebrates, such as zebrafish, Muller glia possess a remarkable capacity for retinal regeneration following various forms of injury through a reprogramming process in which endogenous Muller glia proliferate and differentiate into all types of retinal cells. In mammals, Muller glia become reactive in response to damage to protect or to further impair retinal function. Although mammalian Muller glia have regenerative potential, it is limited as far as repairing damaged retina. Lessons learned from zebrafish will help reveal the critical mechanisms involved in Muller glia reprogramming. Progress has been made in triggering Muller glia to reprogram and generate functional neurons to restore vision in mammals indicating that Muller glia reprogramming may be a promising therapeutic strategy for human retinal diseases. This review comprehensively summarizes the mechanisms related to retinal regeneration in model animals and the critical advanced progress made in Muller glia reprogramming in mammals.
引用
收藏
页码:2342 / 2361
页数:20
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