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Early murine cytomegalovirus (MCMV) infection induces liver natural killer (NK) cell inflammation and protection through macrophage inflammatory protein 1alpha (MIP-1alpha)-dependent pathways

J Exp Med. 1998 Jan 5;187(1):1-14. doi: 10.1084/jem.187.1.1.

Abstract

Natural killer (NK) cells mediate defense against early murine cytomegalovirus (MCMV) infections in liver. The chemokine, macrophage inflammatory protein 1alpha (MIP-1alpha), can promote inflammatory responses. Our studies evaluated contributions of NK cells to early MCMV-induced liver inflammation and MIP-1alpha requirements for inflammation and delivery of antiviral defenses. NK cells were shown to be responsible for focal inflammation, and to be induced to migrate at high levels, in MCMV-infected livers. MIP-1alpha gene expression was elevated at coinciding times, and mice deficient in MIP-1alpha function were dramatically inhibited in both inflammatory and protective liver responses. The results precisely define MIP-1alpha-dependent steps required to achieve NK cell inflammation during, and mechanisms promoting defense against, viral infections in tissues.

Publication types

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

MeSH terms

  • Animals
  • Cell Movement
  • Chemokine CCL3
  • Chemokine CCL4
  • Female
  • Genes, RAG-1
  • Herpesviridae Infections / etiology
  • Herpesviridae Infections / immunology*
  • Herpesviridae Infections / pathology
  • Inflammation / etiology
  • Inflammation / immunology
  • Inflammation / pathology
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / pathology
  • Liver / immunology*
  • Liver / pathology
  • Macrophage Inflammatory Proteins / deficiency
  • Macrophage Inflammatory Proteins / immunology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred CBA
  • Mice, Knockout
  • Mice, Nude
  • Mice, SCID
  • Muromegalovirus*

Substances

  • Chemokine CCL3
  • Chemokine CCL4
  • Macrophage Inflammatory Proteins