NOTCH1 signaling establishes the medullary thymic epithelial cell progenitor pool during mouse fetal development

Development. 2020 Jun 22;147(12):dev178988. doi: 10.1242/dev.178988.

Abstract

The cortical and medullary thymic epithelial cell (cTEC and mTEC) lineages are essential for inducing T cell lineage commitment, T cell positive selection and the establishment of self-tolerance, but the mechanisms controlling their fetal specification and differentiation are poorly understood. Here, we show that notch signaling is required to specify and expand the mTEC lineage. Notch1 is expressed by and active in TEC progenitors. Deletion of Notch1 in TECs resulted in depletion of mTEC progenitors and dramatic reductions in mTECs during fetal stages, consistent with defects in mTEC specification and progenitor expansion. Conversely, forced notch signaling in all TECs resulted in widespread expression of mTEC progenitor markers and profound defects in TEC differentiation. In addition, lineage-tracing analysis indicated that all mTECs have a history of receiving a notch signal, consistent with notch signaling occurring in mTEC progenitors. These data provide strong evidence for a requirement for notch signaling in specification of the mTEC lineage.

Keywords: Foxn1; Lineage; Notch; Thymus; mTEC.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation
  • Cell Lineage
  • Embryo, Mammalian / cytology
  • Embryo, Mammalian / metabolism
  • Embryonic Development
  • Epithelial Cells / cytology
  • Epithelial Cells / metabolism
  • Fetal Development / genetics*
  • Forkhead Transcription Factors / deficiency
  • Forkhead Transcription Factors / genetics
  • Forkhead Transcription Factors / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Organogenesis
  • Receptor, Notch1 / deficiency
  • Receptor, Notch1 / genetics
  • Receptor, Notch1 / metabolism*
  • Signal Transduction
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • T-Lymphocytes / cytology
  • T-Lymphocytes / metabolism
  • Thymus Gland / cytology
  • Thymus Gland / growth & development
  • Thymus Gland / metabolism*

Substances

  • Forkhead Transcription Factors
  • Notch1 protein, mouse
  • Receptor, Notch1
  • Whn protein