HINT1 peptide/Hsp70 complex induces NK-cell-dependent immunoregulation in a model of autoimmune demyelination

Grazyna Galazka, Anna Jurewicz, Malgorzata Domowicz, Barbara Cannella, Cedric S. Raine, Krzysztof Selmaj

Research output: Contribution to journalArticle

8 Scopus citations

Abstract

Heat shock proteins (Hsps) interact with the immune system and have been shown to contribute to immunoregulation. As efficient chaperones, Hsps bind many peptides and these complexes have many yet-to-be-clarified functions. We have shown that Hsp70 is complexed within the mouse CNS with peptide CLAFHDISPQAPTHFLVIPK derived from histidine triad nucleotide-binding protein-1 (HINT138-57/Hsp70). Only this complex, in contrast to other peptides complexed with Hsp70, was able to prevent experimental autoimmune encephalomyelitis (EAE) by induction of immunoregulatory mechanisms dependent on NK cells. Pretreatment of proteolipid protein peptide 139-151 (PLP139-151) sensitized SJL/J mice with HINT138-57/Hsp70 prevented the development of EAE, suppressed PLP139-151-induced T-cell proliferation, and blocked secretion of IL-17. HINT138-57/Hsp70 stimulation of NK cells depended on synergistic activation of two NK-cell receptors, CD94 and NKG2D. NK cells with depleted CD94 or with blocked NKG2D did not inhibit PLP139-151-induced spleen cell (SC) proliferation. The HINT138-57/Hsp70 complex enhanced surface expression of the NKG2D ligand-H60. Downstream signaling of CD94 and NKG2D converged at the adaptor proteins DAP10 and DAP12, and in response to HINT138-57/Hsp70 stimulation, expression of DAP10 and DAP12 was significantly increased in NK cells. Thus, we have shown that the HINT138-57/Hsp70 complex affects NK-cell function by enhancing NK-cell-dependent immunoregulation in the EAE model of autoimmune demyelination.

Original languageEnglish (US)
Pages (from-to)3026-3044
Number of pages19
JournalEuropean Journal of Immunology
Volume44
Issue number10
DOIs
StatePublished - Oct 1 2014

Keywords

  • Autoimmunity
  • Experimental autoimmune encephalomyelitis/multiple sclerosis
  • Heat shock protein
  • Neuroimmunology
  • Tolerance/Suppression

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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