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Human corneal epithelial cell proliferation by epiregulin and its cross-induction by other EGF family members.
Mol Vis. 2007 Nov 15; 13:2119-28.MV

Abstract

PURPOSE

To investigate the effects of epiregulin, a newly identified member of the epidermal growth factor (EGF) family, on the proliferation of human corneal epithelial cells (HCECs).

METHODS

The proliferation of HCECs was determined by cell counting and BrdU incorporation assays at specific times after exposure to different concentrations of human recombinant epiregulin (0 to 20 ng/ml). Immunohistochemical staining was used to localize epiregulin in cadaveric corneas. RT-PCR and real-time PCR were used to determine the expression levels of epiregulin in cultured and cadaveric HCECs. To examine the interaction between epiregulin and epidermal growth factor receptors (EGFRs), the phosphorylation of ErbB1 and ERK1/ERK2 (ERK1/2) was estimated by western blot analysis in the presence or absence of AG1478, a specific inhibitor of EGFR kinase activity. To search for cross-induction of epiregulin by other EGF family members, the expressions of EGF, heparin-binding epidermal growth factor-like growth factor (HB-EGF), amphiregulin (AR), and transforming growth factor-alpha (TGF-alpha) mRNA were determined by real-time PCR in the presence of 10 ng/ml of epiregulin. Conversely, the expression of epiregulin was also determined following the incubation of HCECs with 10 nM of either of EGF, HB-EGF, TGF-alpha, or AR.

RESULTS

The mRNA of epiregulin was expressed in cultured HCECs and HCECs obtained from cadaveric eyes. Epiregulin was strongly detected in the limbal epithelium and basal epithelium of the peripheral cornea, but it was weakly detected in the central corneal epithelium. HCECs proliferated in the presence of epiregulin in a dose-dependent manner as detected by an increase in cell numbers or in BrdU incorporation. When HCECs were incubated with exogenous epiregulin, the expression of the mRNA of epiregulin was upregulated as detected by real-time PCR, and the phosphorylation of ErbB1 and ERK1/2 was upregulated in a dose-dependent manner as shown by western blot analysis. These upregulations were inhibited by AG1478, a specific inhibitor of EGFR kinase activity. Epiregulin increased the expression of HB-EGF and AR, while TGF-alpha, HB-EGF, AR, and EGF increased the expression of epiregulin in HCECs.

CONCLUSIONS

These findings indicate that epiregulin played an autocrine role in the proliferation of HCECs presumably through cross-induction with other EGF family members.

Authors+Show Affiliations

Department of Ophthalmology, Ehime University School of Medicine, Ehime, Japan. morita21@m.ehime-u.ac.jpNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

18079685

Citation

Morita, Shin-ichi, et al. "Human Corneal Epithelial Cell Proliferation By Epiregulin and Its Cross-induction By Other EGF Family Members." Molecular Vision, vol. 13, 2007, pp. 2119-28.
Morita S, Shirakata Y, Shiraishi A, et al. Human corneal epithelial cell proliferation by epiregulin and its cross-induction by other EGF family members. Mol Vis. 2007;13:2119-28.
Morita, S., Shirakata, Y., Shiraishi, A., Kadota, Y., Hashimoto, K., Higashiyama, S., & Ohashi, Y. (2007). Human corneal epithelial cell proliferation by epiregulin and its cross-induction by other EGF family members. Molecular Vision, 13, 2119-28.
Morita S, et al. Human Corneal Epithelial Cell Proliferation By Epiregulin and Its Cross-induction By Other EGF Family Members. Mol Vis. 2007 Nov 15;13:2119-28. PubMed PMID: 18079685.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Human corneal epithelial cell proliferation by epiregulin and its cross-induction by other EGF family members. AU - Morita,Shin-ichi, AU - Shirakata,Yuji, AU - Shiraishi,Atsushi, AU - Kadota,Yuko, AU - Hashimoto,Koji, AU - Higashiyama,Shigeki, AU - Ohashi,Yuichi, Y1 - 2007/11/15/ PY - 2007/01/26/received PY - 2007/11/12/accepted PY - 2007/12/15/pubmed PY - 2008/1/30/medline PY - 2007/12/15/entrez SP - 2119 EP - 28 JF - Molecular vision JO - Mol. Vis. VL - 13 N2 - PURPOSE: To investigate the effects of epiregulin, a newly identified member of the epidermal growth factor (EGF) family, on the proliferation of human corneal epithelial cells (HCECs). METHODS: The proliferation of HCECs was determined by cell counting and BrdU incorporation assays at specific times after exposure to different concentrations of human recombinant epiregulin (0 to 20 ng/ml). Immunohistochemical staining was used to localize epiregulin in cadaveric corneas. RT-PCR and real-time PCR were used to determine the expression levels of epiregulin in cultured and cadaveric HCECs. To examine the interaction between epiregulin and epidermal growth factor receptors (EGFRs), the phosphorylation of ErbB1 and ERK1/ERK2 (ERK1/2) was estimated by western blot analysis in the presence or absence of AG1478, a specific inhibitor of EGFR kinase activity. To search for cross-induction of epiregulin by other EGF family members, the expressions of EGF, heparin-binding epidermal growth factor-like growth factor (HB-EGF), amphiregulin (AR), and transforming growth factor-alpha (TGF-alpha) mRNA were determined by real-time PCR in the presence of 10 ng/ml of epiregulin. Conversely, the expression of epiregulin was also determined following the incubation of HCECs with 10 nM of either of EGF, HB-EGF, TGF-alpha, or AR. RESULTS: The mRNA of epiregulin was expressed in cultured HCECs and HCECs obtained from cadaveric eyes. Epiregulin was strongly detected in the limbal epithelium and basal epithelium of the peripheral cornea, but it was weakly detected in the central corneal epithelium. HCECs proliferated in the presence of epiregulin in a dose-dependent manner as detected by an increase in cell numbers or in BrdU incorporation. When HCECs were incubated with exogenous epiregulin, the expression of the mRNA of epiregulin was upregulated as detected by real-time PCR, and the phosphorylation of ErbB1 and ERK1/2 was upregulated in a dose-dependent manner as shown by western blot analysis. These upregulations were inhibited by AG1478, a specific inhibitor of EGFR kinase activity. Epiregulin increased the expression of HB-EGF and AR, while TGF-alpha, HB-EGF, AR, and EGF increased the expression of epiregulin in HCECs. CONCLUSIONS: These findings indicate that epiregulin played an autocrine role in the proliferation of HCECs presumably through cross-induction with other EGF family members. SN - 1090-0535 UR - https://www.unboundmedicine.com/medline/citation/18079685/Human_corneal_epithelial_cell_proliferation_by_epiregulin_and_its_cross_induction_by_other_EGF_family_members_ DB - PRIME DP - Unbound Medicine ER -