Protective effect of miR-30b on retinal ganglion cells against oxygen-glucose deprivation in vitro

Authors: Huang Chanjuan,  Huo Yan,  Chen Chen,  Ai Liqianyu,  Zhou Yuanguo,  Ye Jian
DOI: 10.3760/cma.j.issn.2095-0160.2016.05.004
Published 2016-05-10
Cite as Chin J Exp Ophthalmol, 2016,34(5): 396-401.

Abstract                            [Download PDF] [Read Full Text]

Background

Retinal ganglion cell (RGCs) death following ischaemic insult is the major cause of a number of vision-threatening diseases.Recent studies confirmed that micro RNA (miR-30b) can alleviate hypoxy-induced cardiac injury.However, whether miR-30b can protect RGCs against oxygen-glucose deprivation damage is still not ellucidated.

Objective

The aim of this study was to investigate the protective effect of miR-30b on RGCs damage caused by oxygen-glucose deprivation.

Methods

The retinas were isolated from the eyeballs of eight SD rats aged postnatal 24 hours and RGCs were primarily cultured.The cells were divided into the recombinant adeno-associated virus (rAVV) control group, rAAV-miR-30b mimic group and AAV-miR-30b inhibitor group.Then the cells were transfected using rAVV-miR plasmid, rAAV-miR-30b mimic plasmid and AAV-miR-30b inhibitor plasmid, respectively for 6 days with the RGCs∶AAV as 1∶10 000.The cells were cultured with low glucose medium in hypoxygen incubator (5%CO2, 17%N2, 3%O2) or 5%CO2incubator respectively for 24 hours.Cell viability was detected by cell counting kit-8 assay.The expression of Tubulin Ⅲ, a neuron specific marker, was detected by immunofluorescence technology to evaluate the survival of RGCs.The apoptosis and necrosis of the cells were assessed by Hoechst/PI double staining.

Results

The RGCs grew well with round shape and 1—3 processes 7 days after cultured in the normal cells.However, the RGCs were diminished and the cell process disrupted in the oxygen-glucose deprivation group.The relative vability of the cells was 3.310±0.162 in the rAAV-miR-30b mimic group, which was significantly higher than 0.949±0.141 in the rAAV-miR-30b inhibitor group and 0.900±0.181 in the rAAV-miR control group(t=10.508, 10.296, both at P<0.001). It was positively expressed in survival RGCs, with the red fluorescence.The number of Tubulin Ⅲ+cells was (13.800±1.924)/field in the rAAV-miR-30b mimic group, showing a significant increase in comparison with (0.600±0.548)/field in the rAAV-miR-30b inhibitor group and (0.800±1.304)/field in the rAAV-miR control group (t=15.141, 14.912, both at P<0.001). Significant differences were found in the apoptosis rate and necrosis rate among the rAAV-miR-30b mimic group, rAAV-miR control group and PBS group (F=10.851, P=0.002; F=6.378, P=0.013), and the apoptosis rate and necrosis rate in the rAAV-miR-30b mimic group were considerably lower than those in the rAAV-miR control group and PBS group (all at P<0.05).

Conclusions

The oxygen-glucose deprivation models can be established in RGCs by hypooxygic and low-glucose cultivation.rAAV encoding miR-30b mimics transfection can protect RGCs against oxygen-glucose deprivation damage.

Key words:

MicroRNAs/metabolism; Retinal ganglion cells; Cell hypoxia/physiology; Glucose/physiology; RNA interference; Cytoprotection/drug effects; Rats, Sprague-Dawley; Oxygen-glucose deprivation

Contributor Information

Huang Chanjuan
Department of Ophthalmology, Daping Hospital, Third Military Medical University, Chongqing 400042, China
Huo Yan
Chen Chen
Ai Liqianyu
Zhou Yuanguo
Ye Jian
(Read 26 times, 1 visits today)
Updated: February 23, 2023 — 2:44 am