Effect of epidermal growth factor on proliferation and migration of retinal pigment epithelial cells through EGFR/AKT signaling pathway

AIM:To investigate the effect of epidermal growth factor(EGF)on proliferation and migration of retinal pigment epithelial(RPE)cells. <p>METHODS: Human RPE cell lines(ARPE-19 cell)were treated with different doses of EGF. The methyl thiazolyl tetrazolium(MTT)assay was used to detect cell viabil...

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Main Authors: Xiao-Dong Chen, Jian-Yu Yang
Format: Article
Language:English
Published: Press of International Journal of Ophthalmology (IJO PRESS) 2018-02-01
Series:Guoji Yanke Zazhi
Subjects:
Online Access:http://www.ijo.cn/cn_publish/2018/3/201803006.pdf
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spelling doaj-a6a509dc2f784fc19dba58b1fa66764d2020-11-25T00:07:09ZengPress of International Journal of Ophthalmology (IJO PRESS)Guoji Yanke Zazhi1672-51231672-51232018-02-0118342943310.3980/j.issn.1672-5123.2018.3.06Effect of epidermal growth factor on proliferation and migration of retinal pigment epithelial cells through EGFR/AKT signaling pathwayXiao-Dong Chen0Jian-Yu Yang1Department of Ophthalmology, Xi'an No.1 Hospital, Xi'an 710002, Shaanxi Province, China; Xiamen Eye Center of Xiamen University, Xiamen 361000, Fujian Province, ChinaAier Eye Hospital(Kunming), Kunming 650000,Yunnan Province, China.AIM:To investigate the effect of epidermal growth factor(EGF)on proliferation and migration of retinal pigment epithelial(RPE)cells. <p>METHODS: Human RPE cell lines(ARPE-19 cell)were treated with different doses of EGF. The methyl thiazolyl tetrazolium(MTT)assay was used to detect cell viability. The 5-bromodeoxyuridine(BrdU)incorporation assay was used to detect cell proliferation and the “scratch-wound assay” was used to detect cell migration ability. The epidermal growth factor receptor(EGFR)and protein kinase B(AKT)proteins were detected by Western blot. <p>RESULTS:The MTT assay results showed that treatment with 50 and 100ng/mL EGF for 12h increased ARPE-19 cell viability. The BrdU incorporation assay and the “scratch-wound assay” showed that treatment with 100ng/mL EGF for 24h increased ARPE-19 cell proliferation and migration. The Western blot results showed that treatment with 10-100ng/mL EGF for 12h or 100ng/mL EGF for 15-180min increased phosphorylation levels of EGFR and decreased total levels of EGFR. Similarly, treatment with 10-100ng/mL EGF for 12h or 100ng/mL EGF for 15-180min increased phosphorylation levels of AKT, but not affected total levels of AKT. <p>CONCLUSION: EGF affects ARPE-19 cell viability, proliferation and migration through inducing phosphorylation of the EGFR/AKT signaling pathway. The EGFR/AKT signaling pathway might play an important role in abnormal proliferation and migration of RPE cells in proliferative vitreoretinopathy.http://www.ijo.cn/cn_publish/2018/3/201803006.pdfepidermal growth factorepidermal growth factor receptorprotein kinase Bretinal pigment epithelial cellretinal pigment epithelial cell
collection DOAJ
language English
format Article
sources DOAJ
author Xiao-Dong Chen
Jian-Yu Yang
spellingShingle Xiao-Dong Chen
Jian-Yu Yang
Effect of epidermal growth factor on proliferation and migration of retinal pigment epithelial cells through EGFR/AKT signaling pathway
Guoji Yanke Zazhi
epidermal growth factor
epidermal growth factor receptor
protein kinase B
retinal pigment epithelial cell
retinal pigment epithelial cell
author_facet Xiao-Dong Chen
Jian-Yu Yang
author_sort Xiao-Dong Chen
title Effect of epidermal growth factor on proliferation and migration of retinal pigment epithelial cells through EGFR/AKT signaling pathway
title_short Effect of epidermal growth factor on proliferation and migration of retinal pigment epithelial cells through EGFR/AKT signaling pathway
title_full Effect of epidermal growth factor on proliferation and migration of retinal pigment epithelial cells through EGFR/AKT signaling pathway
title_fullStr Effect of epidermal growth factor on proliferation and migration of retinal pigment epithelial cells through EGFR/AKT signaling pathway
title_full_unstemmed Effect of epidermal growth factor on proliferation and migration of retinal pigment epithelial cells through EGFR/AKT signaling pathway
title_sort effect of epidermal growth factor on proliferation and migration of retinal pigment epithelial cells through egfr/akt signaling pathway
publisher Press of International Journal of Ophthalmology (IJO PRESS)
series Guoji Yanke Zazhi
issn 1672-5123
1672-5123
publishDate 2018-02-01
description AIM:To investigate the effect of epidermal growth factor(EGF)on proliferation and migration of retinal pigment epithelial(RPE)cells. <p>METHODS: Human RPE cell lines(ARPE-19 cell)were treated with different doses of EGF. The methyl thiazolyl tetrazolium(MTT)assay was used to detect cell viability. The 5-bromodeoxyuridine(BrdU)incorporation assay was used to detect cell proliferation and the “scratch-wound assay” was used to detect cell migration ability. The epidermal growth factor receptor(EGFR)and protein kinase B(AKT)proteins were detected by Western blot. <p>RESULTS:The MTT assay results showed that treatment with 50 and 100ng/mL EGF for 12h increased ARPE-19 cell viability. The BrdU incorporation assay and the “scratch-wound assay” showed that treatment with 100ng/mL EGF for 24h increased ARPE-19 cell proliferation and migration. The Western blot results showed that treatment with 10-100ng/mL EGF for 12h or 100ng/mL EGF for 15-180min increased phosphorylation levels of EGFR and decreased total levels of EGFR. Similarly, treatment with 10-100ng/mL EGF for 12h or 100ng/mL EGF for 15-180min increased phosphorylation levels of AKT, but not affected total levels of AKT. <p>CONCLUSION: EGF affects ARPE-19 cell viability, proliferation and migration through inducing phosphorylation of the EGFR/AKT signaling pathway. The EGFR/AKT signaling pathway might play an important role in abnormal proliferation and migration of RPE cells in proliferative vitreoretinopathy.
topic epidermal growth factor
epidermal growth factor receptor
protein kinase B
retinal pigment epithelial cell
retinal pigment epithelial cell
url http://www.ijo.cn/cn_publish/2018/3/201803006.pdf
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