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Vahl, J.C.* ; Drees, C.* ; Heger, K.* ; Heink, S.* ; Fischer, J.C.* ; Nedjic, J.* ; Ohkura, N.* ; Morikawa, H.* ; Poeck, H.* ; Schallenberg, S.* ; Rieß, D.* ; Hein, M.Y.* ; Buch, T.* ; Polic, B.* ; Schönle, A.* ; Zeiser, R.* ; Schmitt-Gräff, A.* ; Kretschmer, K.* ; Klein, L.* ; Korn, T.* ; Sakaguchi, S.* ; Schmidt-Supprian, M.*

Continuous T cell receptor signals maintain a functional regulatory T cell pool.

Immunity 41, 722-736 (2014)
DOI PMC
Open Access Green as soon as Postprint is submitted to ZB.
Regulatory T (Treg) cells maintain immune homeostasis and prevent inflammatory and autoimmune responses. During development, thymocytes bearing a moderately self-reactive T cell receptor (TCR) can be selected to become Treg cells. Several observations suggest that also in the periphery mature Treg cells continuously receive self-reactive TCR signals. However, the importance of this inherent autoreactivity for Treg cell biology remains poorly defined. To address this open question, we genetically ablated the TCR of mature Treg cells in vivo. These experiments revealed that TCR-induced Treg lineage-defining Foxp3 expression and gene hypomethylation were uncoupled from TCR input in mature Treg cells. However, Treg cell homeostasis, cell-type-specific gene expression and suppressive function critically depend on continuous triggering of their TCR.
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Publication type Article: Journal article
Document type Scientific Article
Language english
Publication Year 2014
HGF-reported in Year 0
ISSN (print) / ISBN 1074-7613
e-ISSN 1097-4180
Journal Immunity
Quellenangaben Volume: 41, Issue: 5, Pages: 722-736 Article Number: , Supplement: ,
Publisher Cell Press
Publishing Place Cambridge, Mass.
Reviewing status Peer reviewed
Institute(s) Institute of Pancreatic Islet Research (IPI)
PubMed ID 25464853
Erfassungsdatum 2014-12-31