Disruption of nuclear factor-interleukin-6, a transcription factor, results in severe mycobacterial infection

Am J Pathol. 2001 Feb;158(2):361-6. doi: 10.1016/S0002-9440(10)63977-6.

Abstract

Nuclear factor-interleukin-6 (NF-IL-6) is one of several nuclear transcription factors (NF-IL-6, NF-kappaB, PU.1, interferon-regulatory factor 1, Egr-1, and Stat-1). NF-IL-6 and NF-kappaB are expressed in macrophages and is induced by bacterial lipopolysaccharides. To evaluate whether NF-IL-6 is required for the inflammatory immune response to mycobacterial infection, in which epithelioid macrophages comprise the leading cell population, we generated NF-IL-6 knockout (KO) mutant mice. Airborne infection of these mice with Mycobacterium tuberculosis strains induced disseminated tuberculosis lacking granuloma formation, although interferon-gamma, tumor necrosis factor-alpha, and interleukin-12 mRNA expression levels were within the normal range compared with those of wild-type mice. Generation of O2- and mycobacterial killing by neutrophils from these mice were impaired severely compared with wild-type mice. We conclude that NF-IL-6 is a critical transcription factor in mycobacterial control as well as in granulocyte-colony stimulating factor induction resulting in neutrophil activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Colony Count, Microbial
  • Cytokines / genetics
  • Female
  • Granulocyte Colony-Stimulating Factor / genetics
  • Interferon-alpha / genetics
  • Interferon-gamma / genetics
  • Interleukin-12 / genetics
  • Interleukin-6 / genetics
  • Interleukin-6 / metabolism*
  • Lung / microbiology
  • Lung / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mycobacterium Infections / genetics
  • Mycobacterium Infections / metabolism
  • Mycobacterium Infections / pathology*
  • Mycobacterium tuberculosis / growth & development
  • Neutrophils / cytology
  • Neutrophils / immunology
  • Nitric Oxide / metabolism
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Survival Analysis
  • Time Factors
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • Cytokines
  • Interferon-alpha
  • Interleukin-6
  • Nuclear Proteins
  • RNA, Messenger
  • Transcription Factors
  • Granulocyte Colony-Stimulating Factor
  • Interleukin-12
  • Nitric Oxide
  • Interferon-gamma