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Targeting Microglia to Treat Degenerative Eye Diseases

Microglia have been implicated in many degenerative eye disorders, including retinitis pigmentosa, age-related macular degeneration, glaucoma, diabetic retinopathy, uveitis, and retinal detachment. While the exact roles of microglia in these conditions are still being discovered, evidence from anima...

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Detalles Bibliográficos
Autores principales: Wang, Sean K., Cepko, Constance L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891158/
https://www.ncbi.nlm.nih.gov/pubmed/35251042
http://dx.doi.org/10.3389/fimmu.2022.843558
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author Wang, Sean K.
Cepko, Constance L.
author_facet Wang, Sean K.
Cepko, Constance L.
author_sort Wang, Sean K.
collection PubMed
description Microglia have been implicated in many degenerative eye disorders, including retinitis pigmentosa, age-related macular degeneration, glaucoma, diabetic retinopathy, uveitis, and retinal detachment. While the exact roles of microglia in these conditions are still being discovered, evidence from animal models suggests that they can modulate the course of disease. In this review, we highlight current strategies to target microglia in the eye and their potential as treatments for both rare and common ocular disorders. These approaches include depleting microglia with chemicals or radiation, reprogramming microglia using homeostatic signals or other small molecules, and inhibiting the downstream effects of microglia such as by blocking cytokine activity or phagocytosis. Finally, we describe areas of future research needed to fully exploit the therapeutic value of microglia in eye diseases.
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spelling pubmed-88911582022-03-04 Targeting Microglia to Treat Degenerative Eye Diseases Wang, Sean K. Cepko, Constance L. Front Immunol Immunology Microglia have been implicated in many degenerative eye disorders, including retinitis pigmentosa, age-related macular degeneration, glaucoma, diabetic retinopathy, uveitis, and retinal detachment. While the exact roles of microglia in these conditions are still being discovered, evidence from animal models suggests that they can modulate the course of disease. In this review, we highlight current strategies to target microglia in the eye and their potential as treatments for both rare and common ocular disorders. These approaches include depleting microglia with chemicals or radiation, reprogramming microglia using homeostatic signals or other small molecules, and inhibiting the downstream effects of microglia such as by blocking cytokine activity or phagocytosis. Finally, we describe areas of future research needed to fully exploit the therapeutic value of microglia in eye diseases. Frontiers Media S.A. 2022-02-17 /pmc/articles/PMC8891158/ /pubmed/35251042 http://dx.doi.org/10.3389/fimmu.2022.843558 Text en Copyright © 2022 Wang and Cepko https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Wang, Sean K.
Cepko, Constance L.
Targeting Microglia to Treat Degenerative Eye Diseases
title Targeting Microglia to Treat Degenerative Eye Diseases
title_full Targeting Microglia to Treat Degenerative Eye Diseases
title_fullStr Targeting Microglia to Treat Degenerative Eye Diseases
title_full_unstemmed Targeting Microglia to Treat Degenerative Eye Diseases
title_short Targeting Microglia to Treat Degenerative Eye Diseases
title_sort targeting microglia to treat degenerative eye diseases
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8891158/
https://www.ncbi.nlm.nih.gov/pubmed/35251042
http://dx.doi.org/10.3389/fimmu.2022.843558
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