Elimination of senescent cells inhibits epithelial-mesenchymal transition of retinal pigment epithelial cells.
Cellular Senescence
Culture Media, Conditioned
/ pharmacology
Dasatinib
/ pharmacology
Epithelial Cells
/ metabolism
Epithelial-Mesenchymal Transition
Humans
Hydrogen Peroxide
/ metabolism
Macular Degeneration
/ metabolism
Quercetin
/ pharmacology
Retinal Pigment Epithelium
/ metabolism
Retinal Pigments
/ metabolism
Transforming Growth Factor beta
/ metabolism
Age-related macular degeneration
Epithelial-mesenchymal transition
Retinal pigment epithelium
Senescence
Journal
Experimental eye research
ISSN: 1096-0007
Titre abrégé: Exp Eye Res
Pays: England
ID NLM: 0370707
Informations de publication
Date de publication:
10 2022
10 2022
Historique:
received:
13
05
2022
revised:
25
07
2022
accepted:
27
07
2022
pubmed:
5
8
2022
medline:
30
9
2022
entrez:
4
8
2022
Statut:
ppublish
Résumé
Age-related macular degeneration (AMD) is one of the most common leading causes of irreversible blindness, and there is no effective treatment for it. It has been reported that aging is the greatest risk factor for AMD, and epithelial-mesenchymal transition (EMT) of retinal pigment epithelium (RPE) cells plays an important role in the pathogenesis of AMD. To clarify the relationship between senescence and EMT in RPE cells, we used the replicative senescence model, H
Identifiants
pubmed: 35926646
pii: S0014-4835(22)00287-1
doi: 10.1016/j.exer.2022.109207
pii:
doi:
Substances chimiques
Culture Media, Conditioned
0
Retinal Pigments
0
Transforming Growth Factor beta
0
Quercetin
9IKM0I5T1E
Hydrogen Peroxide
BBX060AN9V
Dasatinib
RBZ1571X5H
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
109207Informations de copyright
Copyright © 2022 Elsevier Ltd. All rights reserved.
Déclaration de conflit d'intérêts
Declarations of interest None.