Interleukin-1β-induced autophagy-related gene 5 regulates proliferation of embryonic stem cell-derived odontoblastic cells

PLoS One. 2015 Apr 20;10(4):e0124542. doi: 10.1371/journal.pone.0124542. eCollection 2015.

Abstract

We previously established a method for the differentiation of induced pluripotent stem cells and embryonic stem cells into α2 integrin-positive odontoblast-like cells. We also reported that Wnt5 in response to interleukin (IL)-1β induces matrix metalloproteinase (MMP)-3-regulated cell proliferation in these cells. Our findings suggest that MMP-3 plays a potentially unique physiological role in the generation of odontoblast-like cells under an inflammatory state. Here, we examined whether up-regulation of autophagy-related gene (Atg) 5 by IL-1β was mediated by Wnt5 signaling, thus leading to increased proliferation of odontoblast-like cells. IL-1β increased the mRNA and protein levels of Atg5, microtubule-associated protein 1 light chain (LC3, a mammalian homolog of yeast Atg8) and Atg12. Treatment with siRNAs against Atg5, but not LC3 and Atg12, suppressed the IL-1β-induced increase in MMP-3 expression and cell proliferation. Our siRNA analyses combined with western blot analysis revealed a unique sequential cascade involving Atg5, Wnt5a and MMP-3, which resulted in the potent increase in odontoblastic cell proliferation. These results demonstrate the unique involvement of Atg5 in IL-1β-induced proliferation of embryonic stem cell-derived odontoblast-like cells.

Publication types

  • Research Support, Non-U.S. Gov't
  • Retracted Publication

MeSH terms

  • Animals
  • Autophagy-Related Protein 5
  • Cell Differentiation / drug effects
  • Cell Line
  • Cell Proliferation / drug effects
  • Embryonic Stem Cells / cytology*
  • Embryonic Stem Cells / drug effects*
  • Embryonic Stem Cells / metabolism
  • Gene Expression Regulation, Enzymologic / drug effects
  • Gene Silencing
  • Matrix Metalloproteinase 3 / metabolism
  • Mice
  • Microtubule-Associated Proteins / deficiency
  • Microtubule-Associated Proteins / genetics
  • Microtubule-Associated Proteins / metabolism*
  • Odontoblasts / cytology*
  • Proteins / genetics
  • Proteins / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / genetics
  • Rats
  • Signal Transduction / drug effects
  • Wnt Proteins / genetics
  • Wnt Proteins / metabolism

Substances

  • Atg5 protein, mouse
  • Atg5 protein, rat
  • Autophagy-Related Protein 5
  • Microtubule-Associated Proteins
  • Proteins
  • RNA, Messenger
  • RNA, Small Interfering
  • Wnt Proteins
  • Matrix Metalloproteinase 3

Grants and funding

This work was supported by the Japan Society for the Promotion of Science KAKENHI (grant numbers: 26462903 and 26462904).