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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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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