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Lückerath, K.* ; Kirkin, V.* ; Melzer, I.M.* ; Thalheimer, F.B.* ; Siele, D.* ; Milani, W.* ; Adler, T.* ; Aguilar-Pimentel, J.A.* ; Horsch, M. ; Michel, G. ; Beckers, J. ; Busch, D.H.* ; Ollert, M.* ; Gailus-Durner, V. ; Fuchs, H. ; Hrabě de Angelis, M. ; Staal, F.J.* ; Rajalingam, K.* ; Hueber, A.O.* ; Strobl, L.J. ; Zimber-Strobl, U. ; Zörnig, M.*

Immune modulation by Fas ligand reverse signaling: Lymphocyte proliferation is attenuated by the intracellular Fas ligand domain.

Blood 117, 519-529 (2011)
Verlagsversion Volltext DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Fas Ligand (FasL) not only induces apoptosis in Fas receptor-bearing target cells, it is also able to transmit signals into the FasL-expressing cell via its intracellular domain (ICD). Recently, we described a Notch-like proteolytic processing of FasL that leads to the release of the FasL intracellular domain (ICD) into the cytoplasm and subsequent translocation into the nucleus where it may influence gene transcription. To study the molecular mechanism underlying such reverse FasL signaling in detail and to analyze its physiological importance in vivo, we established a knockout/knockin mouse model in which wildtype FasL was replaced with a deletion mutant lacking the ICD. Our results demonstrate that FasL ICD signaling impairs activation-induced proliferation in B and T cells by diminishing phosphorylation of PLCγ, PKC and ERK1/2. We also demonstrate that the FasL ICD interacts with the transcription factor Lymphoid-enhancer binding factor-1 (Lef-1) and inhibits Lef-1-dependent transcription. In vivo, plasma cell numbers, generation of germinal center B cells and, consequently, production of antigen-specific IgM antibodies in response to immunization with T cell-dependent (TD) or T cell-independent (TI) antigen are negatively affected in presence of the FasL ICD, suggesting that FasL reverse signaling participates in negative fine-tuning of certain immune responses.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter PROTEIN-TYROSINE-PHOSPHATASE; T-CELLS; B-CELLS; SECRETORY LYSOSOMES; CYTOPLASMIC TAIL; SCHWANN-CELLS; EXPRESSION; ACTIVATION; DEATH; WNT
ISSN (print) / ISBN 0006-4971
e-ISSN 1528-0020
Zeitschrift Blood
Quellenangaben Band: 117, Heft: 2, Seiten: 519-529 Artikelnummer: , Supplement: ,
Verlag American Society of Hematology
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute for Allergy Research (IAF)
Institute of Virology (VIRO)
Institute of Experimental Genetics (IEG)
Research Unit Gene Vector (AGV)