Submitted February 21, 2006
Accepted July 24, 2006
Stimulated plasmacytoid dendritic cells impair human T cell development
Heike Schmidlin, Wendy Dontje, Fedde Groot, Suzanne J Ligthart, Arnaud D Colantonio, Monique E Oud, Esther J Schilder-Tol, Marcel Spaargaren, Hergen Spits, Christel H Uittenbogaart, and Bianca Blom*
Department of Cell Biology and Histology, Academic Medical Center, University of Amsterdam
UCLA Center for the Health Sciences
Department of Pathology, Academic Medical Center, University of Amsterdam
* Corresponding author; email: b.blom{at}amc.uva.nl.
Thymic plasmacytoid dendritic cells (pDCs) are located predominantly in the medulla and at the cortical-medullary junction, the entry site of bone marrow derived multipotential precursor cells into the thymus, allowing for interactions between thymic pDCs and precursor cells. We demonstrate that in vitro generated pDCs stimulated with CpG or virus impaired the development of human autologous CD34+CD1a- thymic progenitor cells into the T cell lineage. Rescue by addition of neutralizing type I interferon (IFN) antibodies strongly implies that endogenously produced IFN-
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is responsible for this inhibitory effect. Consistent with this notion we show that exogenously added IFN- had a similar impact on IL-7 and Notch-ligand induced development of thymic CD34+CD1a- progenitor cells into T cells, since induction of CD1a, CD4, CD8 and TCR/CD3 surface expression and rearrangements of TCR V-DJ gene segments were severely impaired. In addition, IL-7 induced proliferation, but not survival of the developing thymic progenitor cells was strongly inhibited by IFN-. It is evident from our data that IFN- inhibits the IL-7R signal transduction pathway, although this could not be attributed to interference with either IL-7R proximal (STAT5, Akt/PKB, Erk1/2) or distal (p27kip1, pRb) events.
