Sequential phases in the development of Aire‐expressing medullary thymic epithelial cells involve distinct cellular input

AJ White, DR Withers, SM Parnell… - European journal of …, 2008 - Wiley Online Library
AJ White, DR Withers, SM Parnell, HS Scott, D Finke, PJL Lane, EJ Jenkinson, G Anderson
European journal of immunology, 2008Wiley Online Library
Intrathymic deletion of immature thymocytes that express self‐reactive TCR specificities is
essential in the generation of self tolerance. Medullary thymic epithelial cells (mTEC)
expressing the transcriptional regulator Aire play a key role in this process by regulating
expression of tissue‐restricted antigens to ensure tolerance to peripheral tissues. Here, we
have analysed the cellular and molecular requirements for the initial appearance of Aire+
mTEC in the embryonic thymus, in addition to their persistence in the adult thymus. Analysis …
Abstract
Intrathymic deletion of immature thymocytes that express self‐reactive TCR specificities is essential in the generation of self tolerance. Medullary thymic epithelial cells (mTEC) expressing the transcriptional regulator Aire play a key role in this process by regulating expression of tissue‐restricted antigens to ensure tolerance to peripheral tissues. Here, we have analysed the cellular and molecular requirements for the initial appearance of Aire+ mTEC in the embryonic thymus, in addition to their persistence in the adult thymus. Analysis of thymic ontogeny shows that the emergence of embryonic Aire+ mTEC occurs prior to the appearance of mature thymocytes, and depends upon lymphoid tissue inducer cells expressing retinoic acid receptor‐related orphan receptor γ. In the adult thymus, we show that Aire+ mTEC develop in the absence of thymocyte positive and negative selection and CD40 signalling, but are present at reduced frequency. Collectively these data support a model where the initial differentiation of Aire+ mTEC involves receptor activator of NF‐κB (RANK)‐RANKL interactions with lymphoid tissue inducer cells, with subsequent mTEC turnover and/or survival involving CD40‐mediated signalling following interactions with mature CD4+ thymocytes that express CD40L.
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