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Association of distinct tetraspanins with MHC class II molecules at different subcellular locations in human immature dendritic cells
Author(s) -
Anneke Engering,
Jean Pieters
Publication year - 2001
Publication title -
international immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.86
H-Index - 134
eISSN - 1460-2377
pISSN - 0953-8178
DOI - 10.1093/intimm/13.2.127
Subject(s) - mhc class ii , tetraspanin , mhc class i , cd74 , microbiology and biotechnology , cd1 , biology , antigen , mhc restriction , antigen presentation , transporter associated with antigen processing , c c chemokine receptor type 7 , major histocompatibility complex , t cell , dendritic cell , antigen processing , antigen presenting cell , immunology , cell , immune system , biochemistry , chemokine , chemokine receptor
Dendritic cells have the capacity to trigger T cell responses in lymphoid organs against antigens captured in the periphery. T cell stimulation depends on the ability of MHC class II molecules to present peptides at the cell surface that are acquired in MHC class II compartments. The high capacity of dendritic cells to stimulate T lymphocytes is related to their ability to regulate the distribution of MHC class II molecules intracellularly. To analyze the molecular components involved in the generation of MHC class II-peptide complexes in human immature dendritic cells, mAb were raised against purified MHC class II compartments. One of the antigens turned out to be CD63, a member of the tetraspanin superfamily. CD63 localized exclusively intracellularly where it associated with peptide-loaded class II molecules. In contrast, the tetraspanins CD9, CD53 and CD81 associated with class II molecules at the plasma membrane. Selective association of distinct tetraspanins may be involved in the regulation of MHC class II distribution in human dendritic cells.

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