Polarity and epithelial-mesenchymal transition of retinal pigment epithelial cells in proliferative vitreoretinopathy

Under physiological conditions, retinal pigment epithelium (RPE) is a cellular monolayer composed of mitotically quiescent cells. Tight junctions and adherens junctions maintain the polarity of RPE cells, and are required for cellular functions. In proliferative vitreoretinopathy (PVR), upon retinal...

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Main Authors: Hui Zou, Chenli Shan, Linlin Ma, Jia Liu, Ning Yang, Jinsong Zhao
Format: Article
Language:English
Published: PeerJ Inc. 2020-10-01
Series:PeerJ
Subjects:
Online Access:https://peerj.com/articles/10136.pdf
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spelling doaj-a9439c3532504835aadcd7f55c9321382020-11-25T03:05:29ZengPeerJ Inc.PeerJ2167-83592020-10-018e1013610.7717/peerj.10136Polarity and epithelial-mesenchymal transition of retinal pigment epithelial cells in proliferative vitreoretinopathyHui Zou0Chenli Shan1Linlin Ma2Jia Liu3Ning Yang4Jinsong Zhao5Eye Center, The Second Hospital of Jilin University, Changchun, ChinaEye Center, The Second Hospital of Jilin University, Changchun, ChinaEye Center, The Second Hospital of Jilin University, Changchun, ChinaEye Center, The Second Hospital of Jilin University, Changchun, ChinaEye Center, The Second Hospital of Jilin University, Changchun, ChinaEye Center, The Second Hospital of Jilin University, Changchun, ChinaUnder physiological conditions, retinal pigment epithelium (RPE) is a cellular monolayer composed of mitotically quiescent cells. Tight junctions and adherens junctions maintain the polarity of RPE cells, and are required for cellular functions. In proliferative vitreoretinopathy (PVR), upon retinal tear, RPE cells lose cell-cell contact, undergo epithelial-mesenchymal transition (EMT), and ultimately transform into myofibroblasts, leading to the formation of fibrocellular membranes on both surfaces of the detached retina and on the posterior hyaloids, which causes tractional retinal detachment. In PVR, RPE cells are crucial contributors, and multiple signaling pathways, including the SMAD-dependent pathway, Rho pathway, MAPK pathways, Jagged/Notch pathway, and the Wnt/β-catenin pathway are activated. These pathways mediate the EMT of RPE cells, which play a key role in the pathogenesis of PVR. This review summarizes the current body of knowledge on the polarized phenotype of RPE, the role of cell-cell contact, and the molecular mechanisms underlying the RPE EMT in PVR, emphasizing key insights into potential approaches to prevent PVR.https://peerj.com/articles/10136.pdfProliferative vitreoretinopathyRetinal pigment epitheliumEpithelial-mesenchymal transitionTight junctionsAdherens junctions
collection DOAJ
language English
format Article
sources DOAJ
author Hui Zou
Chenli Shan
Linlin Ma
Jia Liu
Ning Yang
Jinsong Zhao
spellingShingle Hui Zou
Chenli Shan
Linlin Ma
Jia Liu
Ning Yang
Jinsong Zhao
Polarity and epithelial-mesenchymal transition of retinal pigment epithelial cells in proliferative vitreoretinopathy
PeerJ
Proliferative vitreoretinopathy
Retinal pigment epithelium
Epithelial-mesenchymal transition
Tight junctions
Adherens junctions
author_facet Hui Zou
Chenli Shan
Linlin Ma
Jia Liu
Ning Yang
Jinsong Zhao
author_sort Hui Zou
title Polarity and epithelial-mesenchymal transition of retinal pigment epithelial cells in proliferative vitreoretinopathy
title_short Polarity and epithelial-mesenchymal transition of retinal pigment epithelial cells in proliferative vitreoretinopathy
title_full Polarity and epithelial-mesenchymal transition of retinal pigment epithelial cells in proliferative vitreoretinopathy
title_fullStr Polarity and epithelial-mesenchymal transition of retinal pigment epithelial cells in proliferative vitreoretinopathy
title_full_unstemmed Polarity and epithelial-mesenchymal transition of retinal pigment epithelial cells in proliferative vitreoretinopathy
title_sort polarity and epithelial-mesenchymal transition of retinal pigment epithelial cells in proliferative vitreoretinopathy
publisher PeerJ Inc.
series PeerJ
issn 2167-8359
publishDate 2020-10-01
description Under physiological conditions, retinal pigment epithelium (RPE) is a cellular monolayer composed of mitotically quiescent cells. Tight junctions and adherens junctions maintain the polarity of RPE cells, and are required for cellular functions. In proliferative vitreoretinopathy (PVR), upon retinal tear, RPE cells lose cell-cell contact, undergo epithelial-mesenchymal transition (EMT), and ultimately transform into myofibroblasts, leading to the formation of fibrocellular membranes on both surfaces of the detached retina and on the posterior hyaloids, which causes tractional retinal detachment. In PVR, RPE cells are crucial contributors, and multiple signaling pathways, including the SMAD-dependent pathway, Rho pathway, MAPK pathways, Jagged/Notch pathway, and the Wnt/β-catenin pathway are activated. These pathways mediate the EMT of RPE cells, which play a key role in the pathogenesis of PVR. This review summarizes the current body of knowledge on the polarized phenotype of RPE, the role of cell-cell contact, and the molecular mechanisms underlying the RPE EMT in PVR, emphasizing key insights into potential approaches to prevent PVR.
topic Proliferative vitreoretinopathy
Retinal pigment epithelium
Epithelial-mesenchymal transition
Tight junctions
Adherens junctions
url https://peerj.com/articles/10136.pdf
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