Methotrexate and Triptolide regulate Notch signaling pathway by targeting the Nedd4-Numb axis

Int Immunopharmacol. 2023 Jan:114:109595. doi: 10.1016/j.intimp.2022.109595. Epub 2022 Dec 19.

Abstract

Methotrexate (MTX) is used to treat rheumatoid arthritis, acute leukemia, and psoriasis. MTX can cause certain side effects, such as myelosuppression, while the exact mechanism of myelosuppression caused by MTX is unknown. Notch signaling pathway has been considered to be essential to regulate hematopoietic stem cell (HSC) regeneration and homeostasis, thus contributing to bone marrow hematopoiesis. However, whether MTX affects Notch signaling remains unexplored. Here, our study provides evidence that MTX strongly suppresses the Notch signaling pathway. We found that MTX inhibited the interaction between Nedd4 with Numb, thus restricting K48-linked polyubiquitination of Numb and stabilizing Numb proteins. This in turn inhibited the Notch signaling pathway by reducing Notch1 protein levels. Interestingly, we found that a monomeric drug, Triptolide, is capable of alleviating the inhibitory effect of MTX on Notch signaling pathway. This study promotes our understanding of MTX-mediated regulation of Notch signaling and could provide ideas to alleviate MTX-induced myelosuppression.

Keywords: Methotrexate; Nedd4; Notch; Numb; Triptolide.

MeSH terms

  • Intracellular Signaling Peptides and Proteins / metabolism
  • Membrane Proteins / metabolism
  • Methotrexate* / pharmacology
  • Methotrexate* / therapeutic use
  • Nedd4 Ubiquitin Protein Ligases / metabolism
  • Receptor, Notch1
  • Receptors, Notch* / metabolism
  • Signal Transduction

Substances

  • Membrane Proteins
  • Methotrexate
  • Receptor, Notch1
  • Receptors, Notch
  • triptolide
  • Nedd4 Ubiquitin Protein Ligases
  • Intracellular Signaling Peptides and Proteins