» Articles » PMID: 29432033

Effects of 17β-Estradiol on Activity, Gene and Protein Expression of Superoxide Dismutases in Primary Cultured Human Lens Epithelial Cells

Overview
Journal Curr Eye Res
Publisher Informa Healthcare
Specialty Ophthalmology
Date 2018 Feb 13
PMID 29432033
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: Protective effects of estradiol against HO-induced oxidative stress have been demonstrated in lens epithelial cells. The purpose of this study was to investigate the effects of 17β-estradiol (E2) on the different superoxide dismutase (SOD) isoenzymes, SOD-1, SOD-2, and SOD-3, as well as estrogen receptors (ERs), ERα and ERβ, in primary cultured human lens epithelial cells (HLECs).

Materials And Methods: HLECs were exposed to 0.1 µM or 1 µM E2 for 1.5 h and 24 h after which the effects were studied. Protein expression and immunolocalization of SOD-1, SOD-2, ERα, and ERβ were studied with Western blot and immunocytochemistry. Total SOD activity was measured, and gene expression analyses were performed for SOD1, SOD2, and SOD3.

Results: Increased SOD activity was seen after 1.5 h exposure to both 0.1 µM and 1 µM E2. There were no significant changes in protein or gene expression of the different SODs. Immunolabeling of SOD-1 was evident in the cytosol and nucleus; whereas, SOD-2 was localized in the mitochondria. Both ERα and ERβ were immunolocalized to the nucleus, and mitochondrial localization of ERβ was evident by colocalization with MitoTracker. Both ERα and ERβ showed altered protein expression levels after exposure to E2.

Conclusions: The observed increase in SOD activity after exposure to E2 without accompanying increase in gene or protein expression supports a role for E2 in protection against oxidative stress mediated through non-genomic mechanisms.

Citing Articles

Prevalence and risk factors for age-related cataract in Sweden.

Hugosson M, Ekstrom C Ups J Med Sci. 2020; 125(4):311-315.

PMID: 32757792 PMC: 7594726. DOI: 10.1080/03009734.2020.1802375.


Diallyl Trisulfide Protects Rat Brain Tissue against the Damage Induced by Ischemia-Reperfusion through the Nrf2 Pathway.

Silva-Islas C, Chanez-Cardenas M, Barrera-Oviedo D, Ortiz-Plata A, Pedraza-Chaverri J, Maldonado P Antioxidants (Basel). 2019; 8(9).

PMID: 31540440 PMC: 6770608. DOI: 10.3390/antiox8090410.