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The role of retinal Müller cells in diabetic retinopathy and related therapeutic advances

Diabetic retinopathy (DR) is a significant complication of diabetes. During the pathogenesis of retinal microangiopathy and neuronopathy, activated retinal Müller cells (RMCs) undergo morphological and structural changes such as increased expression of glial fibrillary acidic protein, disturbance of...

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Detalles Bibliográficos
Autores principales: Yang, Shuo, Qi, Shounan, Wang, Chenguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9757137/
https://www.ncbi.nlm.nih.gov/pubmed/36531955
http://dx.doi.org/10.3389/fcell.2022.1047487
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author Yang, Shuo
Qi, Shounan
Wang, Chenguang
author_facet Yang, Shuo
Qi, Shounan
Wang, Chenguang
author_sort Yang, Shuo
collection PubMed
description Diabetic retinopathy (DR) is a significant complication of diabetes. During the pathogenesis of retinal microangiopathy and neuronopathy, activated retinal Müller cells (RMCs) undergo morphological and structural changes such as increased expression of glial fibrillary acidic protein, disturbance of potassium and water transport regulation, and onset of production of a large number of inflammatory and vascular growth factors as well as chemokines. Evidently, activated RMCs are necessary for the pathogenesis of DR; therefore, exploring the role of RMCs in DR may provide a new target for the treatment thereof. This article reviews the mechanism of RMCs involvement in DR and the progress in related treatments.
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spelling pubmed-97571372022-12-17 The role of retinal Müller cells in diabetic retinopathy and related therapeutic advances Yang, Shuo Qi, Shounan Wang, Chenguang Front Cell Dev Biol Cell and Developmental Biology Diabetic retinopathy (DR) is a significant complication of diabetes. During the pathogenesis of retinal microangiopathy and neuronopathy, activated retinal Müller cells (RMCs) undergo morphological and structural changes such as increased expression of glial fibrillary acidic protein, disturbance of potassium and water transport regulation, and onset of production of a large number of inflammatory and vascular growth factors as well as chemokines. Evidently, activated RMCs are necessary for the pathogenesis of DR; therefore, exploring the role of RMCs in DR may provide a new target for the treatment thereof. This article reviews the mechanism of RMCs involvement in DR and the progress in related treatments. Frontiers Media S.A. 2022-12-02 /pmc/articles/PMC9757137/ /pubmed/36531955 http://dx.doi.org/10.3389/fcell.2022.1047487 Text en Copyright © 2022 Yang, Qi and Wang. 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 Cell and Developmental Biology
Yang, Shuo
Qi, Shounan
Wang, Chenguang
The role of retinal Müller cells in diabetic retinopathy and related therapeutic advances
title The role of retinal Müller cells in diabetic retinopathy and related therapeutic advances
title_full The role of retinal Müller cells in diabetic retinopathy and related therapeutic advances
title_fullStr The role of retinal Müller cells in diabetic retinopathy and related therapeutic advances
title_full_unstemmed The role of retinal Müller cells in diabetic retinopathy and related therapeutic advances
title_short The role of retinal Müller cells in diabetic retinopathy and related therapeutic advances
title_sort role of retinal müller cells in diabetic retinopathy and related therapeutic advances
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9757137/
https://www.ncbi.nlm.nih.gov/pubmed/36531955
http://dx.doi.org/10.3389/fcell.2022.1047487
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