Generation of both cortical and Aire(+) medullary thymic epithelial compartments from CD205(+) progenitors

Eur J Immunol. 2013 Mar;43(3):589-94. doi: 10.1002/eji.201243209. Epub 2013 Feb 11.

Abstract

In the adult thymus, the development of self-tolerant thymocytes requires interactions with thymic epithelial cells (TECs). Although both cortical and medullary TECs (cTECs/mTECs) are known to arise from common bipotent TEC progenitors, the phenotype of these progenitors and the timing of the emergence of these distinct lineages remain unclear. Here, we have investigated the phenotype and developmental properties of bipotent TEC progenitors during cTEC/mTEC lineage development. We show that TEC progenitors can undergo a stepwise acquisition of first cTEC and then mTEC hallmarks, resulting in the emergence of a progenitor population simultaneously expressing the cTEC marker CD205 and the mTEC regulator Receptor Activator of NF-κB (RANK). In vivo analysis reveals the capacity of CD205(+) TECs to generate functionally competent cortical and medullary microenvironments containing both cTECs and Aire(+) mTECs. Thus, TEC development involves a stage in which bipotent progenitors can co-express hallmarks of the cTEC and mTEC lineages through sequential acquisition, arguing against a simple binary model in which both lineages diverge simultaneously from bipotent lineage negative TEC progenitors. Rather, our data reveal an unexpected overlap in the phenotypic properties of these bipotent TECs with their lineage-restricted counterparts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AIRE Protein
  • Animals
  • Antigens, CD / metabolism*
  • Cell Differentiation
  • Cell Lineage / immunology
  • Epithelial Cells / cytology*
  • Epithelial Cells / metabolism*
  • Immunophenotyping
  • Lectins, C-Type / metabolism*
  • Mice
  • Minor Histocompatibility Antigens
  • Receptor Activator of Nuclear Factor-kappa B / metabolism
  • Receptors, Cell Surface / metabolism*
  • Thymocytes / cytology*
  • Thymocytes / metabolism*
  • Thymus Gland / cytology*
  • Transcription Factors / metabolism*

Substances

  • Antigens, CD
  • DEC-205 receptor
  • Lectins, C-Type
  • Minor Histocompatibility Antigens
  • Receptor Activator of Nuclear Factor-kappa B
  • Receptors, Cell Surface
  • Transcription Factors