Gupta Sandeep K, Haigh Brendan J, Seyfert Hans-Martin, Griffin Frank J, Wheeler Thomas T
Dairy Foods, AgResearch, Ruakura Research Centre, Hamilton, New Zealand; Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand; Leibniz-Institute for Farm Animal Biology (FBN), Institute for Genome Biology, Dummerstorf, Germany.
Dairy Foods, AgResearch, Ruakura Research Centre, Hamilton, New Zealand.
Dev Comp Immunol. 2017 Mar;68:87-97. doi: 10.1016/j.dci.2016.11.015. Epub 2016 Nov 19.
Activation of innate immune receptors by exogenous substances is crucial for the detection of microbial pathogens and a subsequent inflammatory response. The inflammatory response to microbial lipopolysaccharide via Toll-like receptor 4 (TLR4) is facilitated by soluble accessory proteins, but the role of such proteins in the activation of other pathogen recognition receptors for microbial nucleic acid is not well understood. Here we demonstrate that RNase4 and RNase5 purified from bovine milk bind to Salmonella typhimurium DNA and stimulate pro-inflammatory responses induced by nucleic acid mimetics and S. typhimurium DNA in an established mouse macrophage cell culture model, RAW264.7, as well as in primary bovine mammary epithelial cells. RNase4 and 5 also modulated pro-inflammatory signalling in response to nucleic acids in bovine peripheral blood mononuclear cells, although producing a distinct response. These results support a role for RNase4 and RNase5 in mediating inflammatory signals in both immune and epithelial cells, involving mechanisms that are cell-type specific.
外源性物质激活天然免疫受体对于检测微生物病原体及随后的炎症反应至关重要。可溶性辅助蛋白促进了经由Toll样受体4(TLR4)对微生物脂多糖的炎症反应,但此类蛋白在激活其他微生物核酸病原体识别受体中的作用尚不清楚。在此,我们证明,从牛乳中纯化的核糖核酸酶4(RNase4)和核糖核酸酶5(RNase5)可与鼠伤寒沙门氏菌DNA结合,并在已建立的小鼠巨噬细胞培养模型RAW264.7以及原代牛乳腺上皮细胞中,刺激由核酸模拟物和鼠伤寒沙门氏菌DNA诱导的促炎反应。RNase4和RNase5还可调节牛外周血单核细胞对核酸的促炎信号传导反应,尽管产生的反应有所不同。这些结果支持RNase4和RNase5在介导免疫细胞和上皮细胞炎症信号中发挥作用,涉及细胞类型特异性机制。