Inhibition of miR-29a-3p Alleviates Apoptosis of Lens Epithelial Cells via Upregulation of CAND1

Rui Fang1, Hai-Long Li2, Ning-Xin Lv1

  • 1Beijing Tongren Hospital, Capital Medical University, Beijing, China.

Current Eye Research
|December 14, 2023
PubMed
Abstract

Insights

MicroRNA-29a-3p (miR-29a-3p) is downregulated in cataracts. It inhibits lens epithelial cell apoptosis by regulating CAND1, suggesting it’s a potential therapeutic target for senile cataracts.

Area of Science:

  • Ophthalmology
  • Molecular Biology
  • Genetics

Background:

  • MicroRNAs (miRNAs) play a crucial role in the development and progression of senile cataracts.
  • Understanding the specific roles of individual miRNAs in cataractogenesis is essential for developing targeted therapies.

Purpose of the Study:

  • To investigate the role of miR-29a-3p in cataractogenesis.
  • To elucidate the molecular mechanism by which miR-29a-3p influences cataract development.

Main Methods:

  • A rat model of selenite-induced cataracts was established.
  • Whole transcriptome sequencing was employed to identify relevant miRNAs.
  • In vivo and in vitro experiments included CCK8 assay, flow cytometry, luciferase reporter assay, Edu assay, and western blot analysis.

Main Results:

  • Sequencing revealed downregulation of miR-29a-3p in rats with selenite cataracts.
  • Downregulation of miR-29a-3p promoted lens epithelial cell proliferation and inhibited apoptosis.
  • miR-29a-3p directly targets CAND1, and its silencing inhibited cataract development.

Conclusions:

  • miR-29a-3p inhibits lens epithelial cell apoptosis through regulation of CAND1.
  • miR-29a-3p represents a potential therapeutic target for managing senile cataracts.