Inhibition of miR-542-3p augments autophagy to promote diabetic corneal wound healing

• Published in: Eye and vision (Novato, Calif.) Vol. 11; no. 1; p. 3
• Main Authors: Liao, Danling, Wei, Shijia, Hu, Jianzhang
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 03.01.2024; BioMed Central; BMC
• Subjects: Antibodies; ATG4D; Autophagy; Care and treatment; Cornea; Debridement; Diabetes; Diabetic corneal neuropathy; Diabetics; Experiments; Eyes & eyesight; Fluorescein; Fluorescent antibody technique; Fluorides; Glucose; Immunofluorescence; Laboratory animals; Local anesthesia; MicroRNA; MicroRNAs; miR-542-3p; Nerve regeneration; Nervous system; Neuropeptides; Ophthalmology; Peripheral neuropathy; Proteins; Streptozocin; Tissue engineering; Tubulins; Type 1 diabetes; Wound healing; Wounds and injuries; China; Beijing China; United States > US; Germany; miR-542-3p; Diabetic corneal neuropathy; Autophagy; Nerve regeneration; ATG4D
• ISSN: 2326-0254; 2326-0246; 2326-0254
• DOI: 10.1186/s40662-023-00370-1

Autophagy has recently been shown to be critical for protecting peripheral nerve regeneration. This study explored the impact of miR-542-3p on diabetic corneal nerve regeneration and epithelial healing through the regulation of autophagy. A type 1 diabetes model was established in male mice through streptozotocin administration. Immunofluorescence staining of β-Tubulin III and sodium fluorescein staining were performed to observe corneal nerve fiber density and corneal epithelial healing, respectively. Western blotting, immunofluorescence and transmission electron microscopy were used to determine autophagy levels. Subconjunctival injection of RAPA and 3-MA altered autophagy levels; with them, we evaluated the role of autophagy in diabetic keratopathy. miRNA sequencing and bioinformatics analysis were performed to identify miRNA-mRNA networks with potential autophagy-regulating roles, and miR-542-3p was measured by quantitative real-time polymerase chain reaction (qRT-PCR). miR-542-3p antagomir was injected subconjunctivally to assess the role in diabetic corneal neuropathy. Our data suggest that autophagy is suppressed in the diabetic corneal nerve and that activation of autophagy promotes diabetic corneal wound healing. We identified a potential autophagy-regulating miRNA-mRNA network in the diabetic trigeminal ganglion, in which miR-542-3p expression was significantly upregulated. Inhibition of miR-542-3p significantly enhanced the level of autophagy in trigeminal ganglion by upregulating ATG4D expression, thereby accelerating diabetic corneal nerve regeneration and epithelial healing. Dysregulated autophagy is an important contributor to delayed diabetic corneal injury healing. Inhibiting miR-542-3p promotes diabetic corneal nerve regeneration and epithelial healing through autophagy activation by ATG4D.