Effects of Histone Deacetylase Inhibitor (Valproic Acid) on the Expression of Hypoxia-inducible Factor-1 Alpha in Human Retinal Müller Cells.
- Author:
Young Jun KIM
1
;
Sang Jun PARK
;
Na Rae KIM
;
Hee Seung CHIN
Author Information
- Publication Type:Original Article
- Keywords: Histone deacetylase inhibitors; Hypoxia-inducible factor 1 alpha; Retinal Muller cells; Valproic acid; Vascular endothelial growth factor
- MeSH: Anoxia; Enzyme-Linked Immunosorbent Assay; Ependymoglial Cells; Histone Deacetylase Inhibitors*; Histone Deacetylases*; Histones*; Humans*; Retinaldehyde*; Valproic Acid; Vascular Diseases; Vascular Endothelial Growth Factor A
- From:Korean Journal of Ophthalmology 2017;31(1):80-85
- CountryRepublic of Korea
- Language:English
- Abstract: PURPOSE: To evaluate the effects of valproic acid (VPA), a histone deacetylase inhibitor (HDACI), on the expression of hypoxia-inducible factor-1 alpha (HIF-1α) and vascular endothelial growth factor (VEGF) in human retinal Müller cells under hypoxic conditions. METHODS: Chemical hypoxia was induced in human retinal Müller cells (MIO-M1) by treatment with increasing concentrations of cobalt(II) chloride (CoCl₂). Müller cells were also treated with a set concentration of CoCl₂, along with various concentrations of VPA. The expression of HIF-1α and VEGF in the treated Müller cells was determined by enzyme-linked immunosorbent assay. RESULTS: Exposure of human retinal Müller cells to increasing concentrations of CoCl₂ produced a dose-dependent increase in HIF-1α expression. The addition of increasing concentrations of VPA lead to a dose-dependent decrease in expression of HIF-1α and VEGF in Müller cells exposed to a set concentration of CoCl₂. CONCLUSIONS: HDACI VPA downregulated the expressions of HIF-1α and VEGF in human retinal Müller cells under hypoxic conditions. Using HDACI to target HIF-1α expression in Müller cells could be a new therapeutic strategy for the treatment of retinal vascular diseases.
