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CD40, an extracellular receptor for binding and uptake of Hsp70-peptide complexes

MPG-Autoren
http://pubman.mpdl.mpg.de/cone/persons/resource/persons78072

Hartl,  F. U.
Hartl, Franz-Ulrich / Cellular Biochemistry, Max Planck Institute of Biochemistry, Max Planck Society;

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Zitation

Becker, T., Hartl, F. U., & Wieland, F. (2002). CD40, an extracellular receptor for binding and uptake of Hsp70-peptide complexes. Journal of Cell Biology, 158(7), 1277-1285.


Zitierlink: http://hdl.handle.net/11858/00-001M-0000-0010-6E46-1
Zusammenfassung
Tumor and viral antigens elicit a potent immune response by heat shock protein-dependent uptake of antigenic peptide with subsequent presentation by MHC I. Receptors on antigen- presenting cells that specifically bind and internalize a heat shock protein-peptide complex have not yet been identified. Here, we show that cells expressing CD40, a cell surface protein crucial for B cell function and autoimmunity, specifically bind and internalize human Hsp70 with bound peptide. Binding of Hsp70-peptide complex to the exoplasmic domain of CD40 is mediated by the NH2-terminal nucleotide- binding domain of Hsp70 in its ADP state. The Hsp70 cochaperone Hip, but not the bacterial Hsp70 homologue DnaK, competes formation of the Hsp70-CD40 complex. Binding of Hsp70-ADP to CD40 is strongly increased in the presence of Hsp70 peptide substrate, and induces signaling via p38. We suggest that CD40 is a cochaperone-like receptor mediating the uptake of exogenous Hsp70-peptide complexes by macrophages and dendritic cells.