Transcriptional regulation of Notch1 by nuclear factor-κB during T cell activation

Sci Rep. 2023 Jan 2;13(1):43. doi: 10.1038/s41598-022-26674-1.

Abstract

Notch1 plays important roles in T cell development and is highly expressed in activated CD4+ T cells. However, the underlying mechanism of Notch1 transcription in T cells has not been fully characterized. Therefore, we aimed to determine how Notch1 expression is regulated during the activation of CD4+ T cells. Both the surface expression and mRNA transcription of Notch1 were significantly higher in activated CD4+ T cells, but the inhibition of phosphatidylinositol 3-kinase (PI3K) by LY294002 or deletion of the Pdk1 gene impaired this upregulation of Notch1. Interrogation of the Notch1 promoter region using serially deleted Notch1 promoter reporters revealed that the - 300 to - 270 region is crucial for its transcription in activated T cells. In addition, we found that nuclear factor (NF)-κB subunits containing RelA bind directly to this promoter region, thereby upregulating transcription. In addition, inhibition of NF-κB by SN50 impaired upregulation of Notch1 surface protein and mRNA in activated CD4+ T cells. Thus, we provide evidence that Notch1 transcription in activated CD4+ T cells is upregulated via the PI3K-PDK1-NF-κB signaling pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Gene Expression Regulation
  • NF-kappa B* / metabolism
  • Phosphatidylinositol 3-Kinases* / metabolism
  • RNA, Messenger / metabolism
  • Receptor, Notch1 / genetics
  • Receptor, Notch1 / metabolism
  • T-Lymphocytes / metabolism
  • Transcription Factor RelA / metabolism
  • Transcriptional Activation

Substances

  • NF-kappa B
  • Phosphatidylinositol 3-Kinases
  • Transcription Factor RelA
  • Receptor, Notch1
  • RNA, Messenger