ERK1/2-Dependent Gene Expression Contributing to TGFß-Induced Lens EMT.
Curr Eye Res
; 43(8): 986-997, 2018 08.
Article
em En
| MEDLINE
| ID: mdl-29652528
ABSTRACT
PURPOSE:
This study aims to highlight some of the genes that are differentially regulated by ERK1/2 signaling in TGFß-induced EMT in lens, and their potential contribution to this pathological process. MATERIALS ANDMETHODS:
Rat lens epithelial explants were cultured with or without TGFß over a 3-day-culture period to induce EMT, in the presence or absence of UO126 (ERK1/2 signaling inhibitor), both prior to TGFß-treatment, or 24 or 48 hours after TGFß treatment. Smad2/3-nuclear immunolabeling was used to indicate active TGFß signaling, and quantitative RT-PCR was used to analyze changes in the different treatment groups in expression of the following representative genes TGFß signaling (Smad7, Smurf1, and Rnf111), epithelial markers (Pax6, Cdh1, Zeb1, and Zeb2), cell survival/death regulators (Bcl2, Bax, and Bad) and lens mesenchymal markers (Mmp9, Fn1, and Col1a1), over the 3 days of culture.RESULTS:
ERK1/2 was found to regulate the expression of Smurf1, Smad7, Rnf11, Cdh1, Pax6, Zeb1, Bcl2, Bax, and Bad genes in lens cells. TGFß signaling was evident by nuclear localization of Smad2/3 and this was effectively blocked by pre-treatment with UO126, but not by post-treatment with this ERK1/2 signaling inhibitor. TGFß induced the expression of its signaling partners (Smad7, Smurf1, and Rnf111), as well as lens mesenchymal genes (Mmp9, Fn1, and Col1a1), consistent with its role in inducing an EMT. These TGFß-responsive signaling genes, as well as the mesenchymal markers, were all positively regulated by ERK1/2-activity. The expression levels of the lens epithelial genes we examined, and genes that were associated with cell death/survival, were not directly impacted by TGFß.CONCLUSIONS:
TGFß-mediated ERK1/2 signaling positively modulates the expression of mesenchymal genes in lens epithelial explants undergoing EMT, in addition to regulating TGFß-mediated regulatory genes. Independent of TGFß, ERK1/2 activity can also regulate the expression of endogenous lens epithelial genes, highlighting its potential key role in regulation of both normal and pathological lens cellular processes.Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Catarata
/
Expressão Gênica
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Sistema de Sinalização das MAP Quinases
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Fator de Crescimento Transformador beta2
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Transição Epitelial-Mesenquimal
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Cristalino
Tipo de estudo:
Prognostic_studies
Limite:
Animals
Idioma:
En
Revista:
Curr Eye Res
Ano de publicação:
2018
Tipo de documento:
Article