Cutting edge: heat shock protein gp96 induces maturation and migration of CD11c+ cells in vivo

J Immunol. 2000 Dec 1;165(11):6029-35. doi: 10.4049/jimmunol.165.11.6029.

Abstract

Immunization of mice with the heat shock protein (HSP) gp96 but not control proteins leads to 5- to 7-fold enlargement of draining lymph nodes (LNs) resulting from accumulation of large numbers of mature CD11c(+) cells, but not T or B lymphocytes in them. The increase in size and cellularity is time-dependent; the draining LNs reach their peak size between 12 and 24 h after injection and regress to their normal size between 48 and 72 h after injection. The increment is elicited specifically in the draining LN but not in other LNs. This observation uncovers a novel aspect of HSP-APC interaction and adds to the mechanistic explanation for the unusually high immunogenicity of HSP-peptide complexes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antigen-Presenting Cells / cytology
  • Antigen-Presenting Cells / immunology
  • Antigen-Presenting Cells / metabolism
  • Antigens, Neoplasm / administration & dosage*
  • Antigens, Neoplasm / immunology
  • Antigens, Neoplasm / physiology*
  • Cell Differentiation / immunology
  • Cell Division / immunology
  • Cell Movement / immunology*
  • Growth Substances / administration & dosage*
  • Growth Substances / immunology
  • Growth Substances / physiology*
  • Heat-Shock Proteins / administration & dosage*
  • Heat-Shock Proteins / immunology
  • Heat-Shock Proteins / physiology*
  • Injections, Intradermal
  • Integrin alphaXbeta2 / biosynthesis*
  • Lymph Nodes / anatomy & histology
  • Lymph Nodes / cytology
  • Lymph Nodes / immunology
  • Lymph Nodes / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Organ Size / immunology

Substances

  • Antigens, Neoplasm
  • Growth Substances
  • Heat-Shock Proteins
  • Integrin alphaXbeta2
  • sarcoma glycoprotein gp96 rejection antigens