Corticosteroids effects on LPS-induced rat inflammatory keratocyte cell model

PLoS One. 2017 Apr 27;12(4):e0176639. doi: 10.1371/journal.pone.0176639. eCollection 2017.

Abstract

Purpose: Corticosteroids are efficient anti-inflammation treatments. However, there are still arguments on whether it should be used in keratitis. This study was to observe the effect of corticosteroids on keratocytes both in normal condition and inflammation status in vitro.

Methods: Rat keratocytes were cultured and used for examination. 10 μg/ml lipopolysaccharide (LPS) was used to establish the inflammatory keratocyte cell model, and prednisolone acetate (PA), dexamethasone (Dex) and fluorometholone (Flu) were used as corticosteroids treatments. 5 d-growth curve and cell viabilities were assayed by CCK8, and cell morphologies and migration rate were studied. TNF-α, IL-6 and IL-1β levels were examined by ELISA. Western blotting was used to quantified type VI collagen (Col VI) and matrix metalloproteinase 9 (MMP9) expressions, and immunofluorescence staining assays of Col I and Col VI were carried out.

Results: In normal condition, proliferation and migration of keratocytes were slightly influenced in PA, Dex and Flu groups. The secretion of Col I and Col VI was suppressed and MMP9 expression increased in corticosteroids groups. But no significant difference was seen in TNF-α, IL-6 and IL-1β expression levels. In inflammatory status, TNF-α, IL-6 and MMP9 levels increased in LPS group, while they significantly decreased in corticosteroids groups. Although keratocytes viabilities and migration were slightly affected in 24 h, no significant differences were seen between LPS group and corticosteroids groups in 5-d proliferation. Col I and Col VI secretion in LPS-keratocytes was maintained with corticosteroids treatments.

Conclusions: Corticosteroids showed lightly effects on keratocytes proliferation and migration, but it successfully decreased TNF-α, IL-6 level and maintained the secretion of and Col I and Col VI, while suppressed the expression of MMP9 in LPS-induced keratocytes. PA was suggested to use in early stage of keratitis clinical treatment.

MeSH terms

  • Adrenal Cortex Hormones / pharmacology*
  • Animals
  • Blotting, Western
  • Cells, Cultured
  • Collagen Type VI / metabolism
  • Corneal Keratocytes / drug effects*
  • Corneal Keratocytes / metabolism
  • Corneal Keratocytes / pathology
  • Dexamethasone / pharmacology
  • Enzyme-Linked Immunosorbent Assay
  • Fluorometholone / pharmacology
  • Inflammation / pathology
  • Interleukin-1beta / metabolism
  • Interleukin-6 / metabolism
  • Keratitis / drug therapy
  • Lipopolysaccharides / pharmacology
  • Male
  • Matrix Metalloproteinase 9 / metabolism
  • Prednisolone / analogs & derivatives
  • Prednisolone / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Adrenal Cortex Hormones
  • Collagen Type VI
  • Interleukin-1beta
  • Interleukin-6
  • Lipopolysaccharides
  • Tumor Necrosis Factor-alpha
  • Dexamethasone
  • prednisolone acetate
  • Prednisolone
  • Matrix Metalloproteinase 9
  • Fluorometholone

Grants and funding

This work was supported by https://isisn.nsfc.gov.cn/egrantindex/funcindex/prjsearch-list### National Natural Science Foundation of China to PXW (No.812006592); http://gonggao.gdstc.gov.cn/itemListAction.do?method=Item_List_Select Science and Technology Planning Project of Guangdong Province to PXW (No. 2014A020211011); http://research.sysu.edu.cn/; the Basal Research Fund for the Medical Young Scientists of Sun Yat-sen University to PXW(No. 14ykpy14); http://gonggao.gdstc.gov.cn/itemListAction.do?method=Item_List_Select Science and Technology Planning Project of Guangdong Province to ZW (No. 2016A020214012); http://apply.gzkj.gov.cn/; Science and Technology Planning Project of Guangzhou to ZW (No. 201607010063), and http://gonggao.gdstc.gov.cn/itemListAction.do?method=Item_List_Select Science and Technology Planning Project of Guangdong Province to ZW (No. 2014A010105029). The corresponding authors PXW and ZW were responsible for conceptualization, formal analysis, funding and review in this study.