Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches

被引:6
|
作者
Garcia-Lopez, Marta [1 ]
Arenas, Joaquin [2 ,3 ]
Gallardo, M. Esther [1 ,3 ]
机构
[1] Hosp 12 Octubre I 12, Grp Invest Traslac Con Celulas iPS, Inst Invest Sanitaria, Madrid 28041, Spain
[2] Hosp 12 Octubre I 12, Grp Enfermedades Raras Mitocondriales & Neuromusc, Inst Invest Sanitaria, Madrid 28041, Spain
[3] Ctr Invest Biomed Red CIBERER, Madrid, Spain
关键词
induced pluripotent stem cells; iPSCs; iPS; optic neuropathies; optic atrophy; mitochondriopathy; retinal ganglion cells; organoids; tissue engineering; RETINAL GANGLION-CELLS; CLINICAL-FEATURES; MITOCHONDRIAL DYSFUNCTION; FUNCTIONAL AXONS; NUCLEAR MODIFIER; DRUG DISCOVERY; NEURAL RETINA; IPSC LINE; DIFFERENTIATION; GENERATION;
D O I
10.3390/genes12010112
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Inherited optic neuropathies share visual impairment due to the degeneration of retinal ganglion cells (RGCs) as the hallmark of the disease. This group of genetic disorders are caused by mutations in nuclear genes or in the mitochondrial DNA (mtDNA). An impaired mitochondrial function is the underlying mechanism of these diseases. Currently, optic neuropathies lack an effective treatment, and the implementation of induced pluripotent stem cell (iPSC) technology would entail a huge step forward. The generation of iPSC-derived RGCs would allow faithfully modeling these disorders, and these RGCs would represent an appealing platform for drug screening as well, paving the way for a proper therapy. Here, we review the ongoing two-dimensional (2D) and three-dimensional (3D) approaches based on iPSCs and their applications, taking into account the more innovative technologies, which include tissue engineering or microfluidics.
引用
收藏
页码:1 / 21
页数:21
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