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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 Verlagsversion bestellen
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
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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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
ISSN (print) / ISBN 1074-7613
e-ISSN 1097-4180
Zeitschrift Immunity
Quellenangaben Band: 41, Heft: 5, Seiten: 722-736 Artikelnummer: , Supplement: ,
Verlag Cell Press
Verlagsort Cambridge, Mass.
Begutachtungsstatus Peer reviewed
Institut(e) Institute for Pancreatic Beta Cell Research (IPI)