Literature DB >> 10422859

Differential effects of epidermal growth factor and interleukin 6 on corneal epithelial cells and vascular endothelial cells.

M Nakamura1, T Nishida.   

Abstract

PURPOSE: Epidermal growth factor (EGF) and interleukin 6 (IL-6) stimulate corneal epithelial wound healing. When applied to the cornea, these cytokines act on various types of cells and therefore may induce corneal neovascularization. We investigated the effects of EGF and IL-6 on cell proliferation and cell migration in rabbit corneal epithelial cells and human umbilical vein endothelial cells (HUVECs).
METHODS: Corneal epithelial cells or HUVECs were cultured with EGF or IL-6 in the presence of 1% fetal bovine serum, and the number of cells were counted, or the radioactivity of [3H]thymidine-incorporated cells was measured. Monolayered cultured corneal epithelial cells or HUVECs were mechanically wounded, and then the cells were cultured with serum-free basal medium containing EGF or IL-6. After 12 or 24 h, the wounded area was measured. Corneal blocks were cultured with serum-free TC-199 medium containing EGF or IL-6 for 24 h, and then the length of the path of the corneal epithelium was measured.
RESULTS: Estimated cell count and [3H]thymidine uptake showed that EGF stimulated cell proliferation in both corneal epithelial cells and HUVECs in a dose-dependent manner. In contrast, IL-6 did not affect cell proliferation in either cell type. Furthermore, EGF also stimulated cell migration by increasing the monolayer and organ-culture system in both cells in a dose-dependent fashion. However, IL-6 stimulated cell migration only in corneal epithelial cells and not in HUVECs.
CONCLUSION: These results demonstrated that EGF stimulated cell proliferation and migration in both corneal epithelial cells and HUVECs. In contrast, IL-6 stimulated only corneal epithelial cell migration and did not affect cell proliferation in either cell type or cell migration in HUVECs. These results suggest that, when applied to the cornea, EGF might induce corneal neovascularization, and IL-6 probably would not.

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Year:  1999        PMID: 10422859     DOI: 10.1097/00003226-199907000-00011

Source DB:  PubMed          Journal:  Cornea        ISSN: 0277-3740            Impact factor:   2.651


  13 in total

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2.  Thymosin beta 4: A novel corneal wound healing and anti-inflammatory agent.

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3.  IL-6 induction in desiccated corneal epithelium in vitro and in vivo.

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4.  The effect of topical 0.05% cyclosporine on recurrence following pterygium surgery.

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5.  Proinflammatory gene polymorphisms are potentially associated with Korean non-Sjogren dry eye patients.

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8.  Association Between Atopic Keratoconjunctivitis and the Risk of Recurrent Corneal Erosion.

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9.  Corneal wound healing is compromised by immunoproteasome deficiency.

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Review 10.  Ocular surface mucins and local inflammation--studies in genetically modified mouse lines.

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Journal:  BMC Ophthalmol       Date:  2015-12-17       Impact factor: 2.209

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