MicroRNA-143 Targets ATG2B to Inhibit Autophagy and Increase Inflammatory Responses in Crohn's Disease

Inflamm Bowel Dis. 2018 Mar 19;24(4):781-791. doi: 10.1093/ibd/izx075.

Abstract

Background: Dysfunctional autophagy is recognized as a contributing factor in many chronic inflammatory diseases, including Crohn's disease (CD). Genetic analyses have found that microRNA (miRNA) levels are altered in the intestinal tissues of CD patients.

Methods: The Sequencing Alternative Poly-Adenylation Sites (SAPAS) method was used to compare the 3' end of the total mRNA sequence of 3 surgical specimens of CD patients (including inflamed tissues and corresponding noninflamed tissues in each case). The levels of autophagy-related 2B (ATG2B), LC3, and miR-143 were compared between inflamed tissues and noninflamed tissues using immunoblot and quantitative reverse transcription polymerase chain reaction. Luciferase assays were used to verify the interactions between miR-143 and ATG2B. Autophagy was measured by immunoblot analyses of LC3 and transmission electron microscopy. Inflammatory cytokines and IκBα were analyzed to evaluate the effect of miR-143 on inflammatory response.

Results: The tandem repeat 3'-UTR of ATG2B was longer in inflamed tissues than in corresponding noninflamed tissues and contained an miR-143 target site. miR-143 expression was elevated, whereas ATG2B and LC3-II were downregulated in inflamed tissues. The direct interaction between miR-143 and ATG2B was verified by a 3'-UTR dual-luciferase reporter assay. Constitutive expression of miR-143 or depletion of ATG2B in cultured intestinal epithelial cells inhibited autophagy, reduced IκBα levels, and increased inflammatory responses.

Conclusions: miR-143 may induce bowel inflammation by regulating ATG2B and autophagy, suggesting that miR-143 might play a critical role in the development of CD. Therefore, miR-143 could be a promising novel target for gene therapy in CD patients.

MeSH terms

  • Adult
  • Autophagy / genetics*
  • Autophagy-Related Proteins / genetics*
  • Crohn Disease / genetics*
  • Cytokines / metabolism
  • Female
  • HEK293 Cells
  • HT29 Cells
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Inflammation / metabolism*
  • Male
  • MicroRNAs / genetics*
  • Vesicular Transport Proteins / genetics*
  • Young Adult

Substances

  • ATG2B protein, human
  • Autophagy-Related Proteins
  • Cytokines
  • MIRN143 microRNA, human
  • MicroRNAs
  • Vesicular Transport Proteins