Bacterial DNA induces murine interferon-γ production by stimulation of interleukin-12 and tumor necrosis factor-α

Melissa D Halpern, Roger J. Kurlander, David S. Pisetsky

Research output: Contribution to journalArticle

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Abstract

Bacterial, but not mammalian DNA, can induce interferon-γ (LFN-γ) in murine splenocytes. To elucidate the basis of this activity, we have assessed in vitro cytokine production by C3W/HeJ splenocytes stimulated with either DNA from Escherichia coil or a synthetic oligonucleotide containing an active palindromic sequence identified from DNA. Both DNAs induced IFN-γ production, with the requirement for intact DNA shown by sensitivity to DNase digestion. Fractionated cell populations were evaluated to determine direct or indirect cellular effects of the DNA. Although bacterial DNA failed to induce IPN-γ in the nonadherent cell population, supernatants from adherent cells stimulated by DNA induced IFN-γ production by these cells. Interleukin-1a (IL-12) was detectable in supernatants from DNA-stimulated splenocytes before IFN-γ, and neutralizing antibodies directed against IL-12 markedLy inhibited the induction of IFN-γ. Anti-tumor necrosis factor-α (TNF-α) antibodies also inhibited IFN-γ production, and the combination of both anti-IL-12 and anti-TNF-α could totally inhibit production of IFN-γ. Taken together, these results indicate that the stimulation of IFN-γ production by bacterial DNA is mediated by IL-12 and TNF-α and point to macrophages/monocytes as targets of action of this macromolecule.

Original languageEnglish (US)
Pages (from-to)72-78
Number of pages7
JournalCellular Immunology
Volume167
Issue number1
DOIs
StatePublished - Jan 10 1996
Externally publishedYes

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Bacterial DNA
Interleukin-12
Interferons
Tumor Necrosis Factor-alpha
DNA
Escherichia
Deoxyribonucleases
Interleukins
Neutralizing Antibodies
Oligonucleotides
Population
Monocytes
Digestion
Macrophages
Cytokines
Antibodies

ASJC Scopus subject areas

  • Immunology

Cite this

Bacterial DNA induces murine interferon-γ production by stimulation of interleukin-12 and tumor necrosis factor-α. / Halpern, Melissa D; Kurlander, Roger J.; Pisetsky, David S.

In: Cellular Immunology, Vol. 167, No. 1, 10.01.1996, p. 72-78.

Research output: Contribution to journalArticle

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