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首页> 外文期刊>BioMed research international >Functional Roles of Pattern Recognition Receptors That Recognize Virus Nucleic Acids in Human Adipose-Derived Mesenchymal Stem Cells
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Functional Roles of Pattern Recognition Receptors That Recognize Virus Nucleic Acids in Human Adipose-Derived Mesenchymal Stem Cells

机译:模式识别受体的功能作用,其识别人脂肪衍生的间充质干细胞中病毒核酸的功能

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Human adipose-derived mesenchymal stem cells (hAD-MSCs) are mesenchymal stem cells with the capability to modulate immune responses. Evidence showing that hAD-MSCs could mediate innate immune responses through pattern recognition receptors (PRRs) is increasing. However, the roles of PRRs in regulating the innate sensing of virus nucleic acids (RNA and DNA) in hAD-MSCs have not yet been investigated. This study focused on the abundant expression of PRRs, including Toll-like receptor 3 (TLR3) and retinoic acid-inducible gene I (RIG-I), which recognize viral RNA, and gamma-interferon inducible protein 16 (IFI16), which recognizes viral DNA in hAD-MSCs. Poly(I:C), a synthetic dsRNA analogy, activated TLR3 and RIG-I and induced the expression of type I interferons (IFN-α/β) and antivirus proteins, including IFN-stimulating gene 15,2'5'-oligoadenylate synthetase, and Mx GTPase 1 in hAD-MSCs, which were attenuated by the knockdown of each TLR3 or RIG-I. Synthetic herpes simplex viral DNA (HSV60) activated IFI16 and induced the expression of IFN-α/β and antivirus proteins in hAD-MSCs, which were inhibited by the knockdown of IFI16. Both poly(I:C) and HSV60 induced the expression of IFN-α/β through the phosphorylation of IFN-regulatory factor 3. All these results indicated that PRRs recognizing virus nucleic acids were expressed and can mediate antivirus responses in hAD-MSCs.
机译:人脂肪衍生的间充质干细胞(HAT-MSCs)是间充质干细胞,具有调节免疫应答的能力。证据表明,HAY-MSCs可以通过模式识别受体(PRRS)介导先天免疫应答是增加的。然而,尚未研究PRR在调节病毒核酸(RNA和DNA)的先天性传感中的作用尚未研究。该研究的重点是PRR的丰富表达,包括识别病毒RNA和γ-干扰素可诱导蛋白质16(IFI16)的Toll样受体3(TLR3)和视黄酸诱导基因I(RIG-I),其认可患有的病毒DNA。聚(i:c),合成DsRNA类比,活化的TLR3和钻石I,并诱导I型干扰素(IFN-α/β)和抗病毒蛋白的表达,包括IFN刺激基因15,2'5'-寡键酶合成酶和HAT-MSC的MX GTPAse1,其被每个TLR3或钻头I的敲低衰减。合成疱疹病毒DNA(HSV60)活化IFI16,并诱导IFN-α/β和抗病毒蛋白在HAT-MSC中的表达,其被IFI16的敲低抑制。聚(I:C)和HSV60均通过IFN调节因子3的磷酸化诱导IFN-α/β的表达。所有这些结果表明,表达了识别病毒核酸的PRR,并可在HAT-MSC中介导防病毒反应。

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