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Cutting Edge: CTLs Rapidly Capture Membrane Fragments from Target Cells in a TCR Signaling-Dependent Manner
Author(s) -
Denis Hudrisier,
Joëlle Riond,
Honoré Mazarguil,
Jean Edouard Gairin,
Etienne Joly
Publication year - 2001
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.166.6.3645
Subject(s) - t cell receptor , ctl* , microbiology and biotechnology , major histocompatibility complex , mhc class i , transmembrane protein , peptide , transmembrane domain , t cell , antigen , chemistry , biology , cell membrane , cell , membrane , immune system , receptor , biochemistry , immunology , cd8
Upon encounter of a CTL with a target cell carrying foreign Ags, the TCR internalizes with its ligand, the peptide-MHC class I complex. However, it is unclear how this can happen mechanistically because MHC molecules are anchored to the target cell's surface via a transmembrane domain. By using antigenic peptides and lipids that were fluorescently labeled, we found that CTLs promptly capture target cell membranes together with the antigenic peptide as well as various other surface proteins. This efficient and specific capture process requires sustained TCR signaling. Our observations indicate that this process allows efficient acquisition of the Ag by CTL, which may in turn regulate lymphocyte activation or elimination.

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