Published online Oct 26, 2025. doi: 10.4252/wjsc.v17.i10.110058
Revised: July 10, 2025
Accepted: September 2, 2025
Published online: October 26, 2025
Processing time: 149 Days and 15.7 Hours
MicroRNAs (miRNAs) are small non-coding RNAs of 20-22 nucleotides in length. They have been identified as major regulators in the secretome of mesenchymal stem cells (MSCs) including adipose tissue, bone marrow, Wharton’s jelly, and dental pulp. These MSCs and their secretome with specific miRNAs are known modulators of the immune response, angiogenesis, inflammation, and apoptosis. In this review, the application of MSC-derived miRNAs in treating several ocular conditions including dry eye, glaucoma, and retinal degenerative diseases has been compiled. In addition, the emerging role of MSC-derived extracellular vesicles carrying miRNAs as a major cargo, regulating the target cells in the human eye has been reviewed. Finally, the bioengineering of nanovesicles with specific MSC-derived miRNAs as novel drug therapy has been discussed.
Core Tip: Mesenchymal stem cells (MSCs) are emerging as potent therapeutic agents for ocular degeneration due to their regenerative and immunomodulatory properties. A key mechanism of action is through extracellular vesicles, which deliver bioactive cargoes, particularly microRNAs (miRNAs), to target cells. This review highlights the role of MSC-derived miRNAs in modulating immune responses and promoting repair in ocular diseases such as corneal injury, dry eye, diabetic retinopathy, age-related macular degeneration, retinitis pigmentosa, and glaucoma. It also explores the potential of engineering extracellular vesicles enriched with specific MSC-derived miRNAs as innovative, cell-free therapeutic strategies.
