Dissertation (Metadaten)
Titel:Fas ligand interacting proteins : new insights into complex signaling networks
 
Autor:Qian Jing
 
URN:NBN:urn:nbn:de:gbv:8-diss-11011
 
Fakultät:Mathematisch-Naturwissenschaftliche Fakultät
DDC Sachgebiet:570 Biowissenschaften, Biologie
 
Datum der mdl. Prüfung:08.06.2004
 
Referent(in):Prof. Dr. Thomas C. G. Bosch
Korreferent(en) Korreferentin:PD.Dr. Ottmar Janßen
 
Beschreibung:The Fas ligand is a death factor and a potential signal transducer. Here we show the retrograde signaling of FasL could be demonstrated in human T cells. FasL engagement results in a severe block of T cell activation without increased cell death. In cytotoxic T cells, NK cells , FasL can be located intracellularly in 'secretory lysosomes' and delivered to the immunological synapse upon eg. TCR stimulation. The proline-rich domain (PRD) in the cytosolic portion of FasL is required to prevent direct surface expression of the molecule. With FCH/SH3 family of closely related proteins, it was demonstrated members of this family can interact with FasL and changed the subcellular localization of FasL when co-expressed in non-hematopoietic cells indicating a major role of these interactors in guiding FasL to the lysosomal compartment. The observation that the adapter protein Nck1 co-localizes with the FasL in the area of target cell contact suggested that the TCR-triggered recruitment of Nck1 might result in a directed transport of FasL and associated secretory lysosomes into the forming immunological synapse.
 
Schlagworte:Fas Ligand, co-stimulation, reverse signal transduction, protein transport, secretory lysosomes, FCH/SH3 family, immunological synapse, Nck, proline rich domain
 
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