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细菌DNA通过刺激白细胞介素-12和肿瘤坏死因子-α诱导小鼠产生γ干扰素。

Bacterial DNA induces murine interferon-gamma production by stimulation of interleukin-12 and tumor necrosis factor-alpha.

作者信息

Halpern M D, Kurlander R J, Pisetsky D S

机构信息

Medical Research Service, Durham VA Medical Center, North Carolina 27705, USA.

出版信息

Cell Immunol. 1996 Jan 10;167(1):72-8. doi: 10.1006/cimm.1996.0009.

Abstract

Bacterial, but not mammalian DNA, can induce interferon-gamma (IFN-gamma) in murine splenocytes. To elucidate the basis of this activity, we have assessed in vitro cytokine production by C3H/HeJ splenocytes stimulated with either DNA from Escherichia coli or a synthetic oligonucleotide containing an active palindromic sequence identified from DNA. Both DNAs induced IFN-gamma 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 IFN-gamma in the nonadherent cell population, supernatants from adherent cells stimulated by DNA induced IFN-gamma production by these cells. Interleukin-12 (IL-12) was detectable in supernatants from DNA-stimulated splenocytes before IFN-gamma, and neutralizing antibodies directed against IL-12 markedly inhibited the induction of IFN-gamma. Anti-tumor necrosis factor-alpha (TNF-alpha) antibodies also inhibited IFN-gamma production, and the combination of both anti-IL-12 and anti-TNF-alpha could totally inhibit production of IFN-gamma. Taken together, these results indicate that the stimulation of IFN-gamma production by bacterial DNA is mediated by IL-12 and TNF-alpha and point to macrophages/monocytes as targets of action of this macromolecule.

摘要

细菌DNA而非哺乳动物DNA可在小鼠脾细胞中诱导γ干扰素(IFN-γ)产生。为阐明这种活性的基础,我们评估了用大肠杆菌DNA或含从DNA中鉴定出的活性回文序列的合成寡核苷酸刺激的C3H/HeJ脾细胞在体外产生细胞因子的情况。两种DNA均诱导IFN-γ产生,对DNA酶消化的敏感性表明需要完整的DNA。对分离的细胞群体进行评估以确定DNA对细胞的直接或间接作用。尽管细菌DNA未能在非贴壁细胞群体中诱导IFN-γ产生,但DNA刺激的贴壁细胞的上清液可诱导这些细胞产生IFN-γ。在IFN-γ之前,可在DNA刺激的脾细胞的上清液中检测到白细胞介素-12(IL-12),针对IL-12的中和抗体可显著抑制IFN-γ的诱导。抗肿瘤坏死因子-α(TNF-α)抗体也抑制IFN-γ产生,抗IL-12和抗TNF-α两者联合可完全抑制IFN-γ的产生。综上所述,这些结果表明细菌DNA对IFN-γ产生的刺激是由IL-12和TNF-α介导的,并指出巨噬细胞/单核细胞是这种大分子的作用靶点。

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