Multilineage potential and self-renewal define an epithelial progenitor cell population in the adult thymus.

Cell Rep

Stem Cells and Immune Regeneration Laboratory, Department of Anatomy and Developmental Biology, Monash University, Wellington Road, Clayton, VIC 3800, Australia. Electronic address:

Published: August 2014

AI Article Synopsis

  • Thymic epithelial cells (TECs) are essential for the development of T cells and maintaining self-tolerance, but they decline with age.
  • Researchers identified a specific group of immature thymic epithelial progenitors (TEPCs) in adult thymus, which possess stem/progenitor-like capabilities and can develop into mature TEC lineages.
  • These adult TEPCs are mostly inactive in the body but can form colonies and self-renew in lab conditions, and they retain their ability to differentiate in a supportive thymic environment, providing insights into TEC biology and potential therapeutic approaches for aging and regeneration.

Article Abstract

Thymic epithelial cells (TECs) are critical for T cell development and self-tolerance but are gradually lost with age. The existence of thymic epithelial progenitors (TEPCs) in the postnatal thymus has been inferred, but their identity has remained enigmatic. Here, we assessed the entire adult TEC compartment in order to reveal progenitor capacity is retained exclusively within a subset of immature thymic epithelium displaying several hallmark features of stem/progenitor function. These adult TEPCs generate mature cortical and medullary lineages in a stepwise fashion, including Aire+ TEC, within fetal thymus reaggregate grafts. Although relatively quiescent in vivo, adult TEPCs demonstrate significant in vitro colony formation and self-renewal. Importantly, 3D-cultured TEPCs retain their capacity to differentiate into cortical and medullary TEC lineages when returned to an in vivo thymic microenvironment. No other postnatal TEC subset exhibits this combination of properties. The characterization of adult TEPC will enable progress in understanding TEC biology in aging and regeneration.

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Source
http://dx.doi.org/10.1016/j.celrep.2014.07.029DOI Listing

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