Ocular-Component-Specific miRNA Expression in a Murine Model of Lens-Induced Myopia

Int J Mol Sci. 2019 Jul 24;20(15):3629. doi: 10.3390/ijms20153629.

Abstract

To identify tissues and molecules involved in refractive myopic shift and axial length elongation in a murine lens-induced myopia model, we performed a comprehensive analysis of microRNA (miRNA) expression. Three weeks after negative 30 diopter lens fixation on three-week-old C57BL/6J mice, total RNA was extracted from individual ocular components including cornea, iris, lens, retina, retinal pigment epithelium (RPE)/choroid, and sclera tissue. The miRNA expression analysis was pooled from three samples and carried out using Agilent Mouse miRNA Microarray (8 × 60 K) miRBase21.0. The expression ratio was calculated, and differentially expressed miRNAs were extracted, using GeneSpring GX 14.5. Myopic induction showed a significant myopic refractive change, axial elongation, and choroidal thinning. Through the comprehensive miRNA analysis, several upregulated miRNAs (56 in cornea tissue, 13 in iris tissue, 6 in lens tissue, 0 in retina tissue, 29 in RPE/choroid tissue, and 30 in sclera tissue) and downregulated miRNAs (7 in cornea tissue, 28 in iris tissue, 17 in lens tissue, 9 in retina tissue, 7 in RPE/choroid tissue, and 40 in sclera tissue) were observed. Overlapping expression changes in miRNAs were also found in different ocular components. Some of this miRNA dysregulation may be functionally involved in refractive myopia shift and axial length elongation.

Keywords: lens-induced myopia; miRNA; ocular components.

MeSH terms

  • Animals
  • Cornea / metabolism
  • Cornea / pathology
  • Disease Models, Animal
  • Gene Expression Regulation / genetics
  • Humans
  • Iris / metabolism
  • Lens, Crystalline / metabolism*
  • Lens, Crystalline / pathology
  • Mice
  • MicroRNAs / genetics*
  • Myopia / genetics*
  • Myopia / pathology
  • Retina / metabolism
  • Retina / pathology
  • Retinal Pigment Epithelium / metabolism
  • Retinal Pigment Epithelium / pathology
  • Sclera / metabolism

Substances

  • MicroRNAs