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

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 underl...

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Autores principales: García-López, Marta, Arenas, Joaquín, Gallardo, M. Esther
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831942/
https://www.ncbi.nlm.nih.gov/pubmed/33477675
http://dx.doi.org/10.3390/genes12010112
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author García-López, Marta
Arenas, Joaquín
Gallardo, M. Esther
author_facet García-López, Marta
Arenas, Joaquín
Gallardo, M. Esther
author_sort García-López, Marta
collection PubMed
description 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.
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spelling pubmed-78319422021-01-26 Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches García-López, Marta Arenas, Joaquín Gallardo, M. Esther Genes (Basel) Review 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. MDPI 2021-01-18 /pmc/articles/PMC7831942/ /pubmed/33477675 http://dx.doi.org/10.3390/genes12010112 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
García-López, Marta
Arenas, Joaquín
Gallardo, M. Esther
Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches
title Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches
title_full Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches
title_fullStr Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches
title_full_unstemmed Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches
title_short Hereditary Optic Neuropathies: Induced Pluripotent Stem Cell-Based 2D/3D Approaches
title_sort hereditary optic neuropathies: induced pluripotent stem cell-based 2d/3d approaches
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831942/
https://www.ncbi.nlm.nih.gov/pubmed/33477675
http://dx.doi.org/10.3390/genes12010112
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