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. Author manuscript; available in PMC: 2023 Jul 1.
Published in final edited form as: Prog Retin Eye Res. 2022 Jan 4;89:101039. doi: 10.1016/j.preteyeres.2021.101039

Table 2.

Summary of miRNAs in the diabetic cornea and TG

Name Change (DM vs. NL) Functions References
miR-146a ↑ in cornea Delay epithelial wound healing.
Inhibit epithelial cells migration.
Limbal epithelial cells (LEC) maintenance.
Reduce p-p38 and p-EGFR expression.
(Funari et al., 2013; Winkler et al., 2014)
miR-424 ↑ in cornea Delay epithelial wound healing.
Reduce p-p38 and p-EGFR expression
(Funari et al., 2013)
miR-10b ↑ in corneal limbus Increase corneal epithelial cell proliferation.
LESC maintenance and/or their early differentiation.
(Kulkarni et al., 2017)
miR-182 ↓ in TG Promote nerve regeneration.
Recovery of corneal sensation.
Decrease its target gene NOX4.
(Wang et al., 2016)
miR-204–5p ↑ in corneal epithelia Upregulate Sirt1.
Delay epithelial cell cycle.
Inhibit corneal epithelial wound healing.
(Gao et al., 2015a)
miR-409–3p / Upregulate c-Met.
Accelerate epithelial wound healing
(Kramerov et al., 2021)
miR-181a ↑ in TG Decrease nerve regeneration.
Alleviate corneal epithelium healing.
Decrease ATG5-mediated autophagic activation.
Reduce BCL-2-mediated inhibition of apoptosis.
(Hu et al., 2020)
miR-214 ↓ in corneal endothelium Attenuate high glucose induced pyroptosis. (Zhang et al., 2020c)
miR-34c ↑ in TG Affect the growth of trigeminal sensory neurons.
Affect the repair of diabetic corneal nerve endings.
Inhibit autophagy by acting directly on Atg4B.
(Hu et al., 2019)