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本文引用的文献

1
Volatile Anesthetic Sevoflurane Attenuates Toll-Like Receptor 1/2 Activation.挥发性麻醉剂七氟醚可减弱 Toll 样受体 1/2 的激活。
Anesth Analg. 2020 Aug;131(2):631-639. doi: 10.1213/ANE.0000000000004741.
2
Volatile anesthetics isoflurane and sevoflurane directly target and attenuate Toll-like receptor 4 system.挥发性麻醉剂异氟烷和七氟烷直接靶向并减弱 Toll 样受体 4 系统。
FASEB J. 2019 Dec;33(12):14528-14541. doi: 10.1096/fj.201901570R. Epub 2019 Nov 2.
3
The volatile anesthetic sevoflurane reduces neutrophil apoptosis Fas death domain-Fas-associated death domain interaction.挥发性麻醉剂七氟醚可减少中性粒细胞凋亡 Fas 死亡结构域 Fas 相关死亡结构域相互作用。
FASEB J. 2019 Nov;33(11):12668-12679. doi: 10.1096/fj.201901360R. Epub 2019 Aug 30.
4
Damage- and pathogen-associated molecular patterns play differential roles in late mortality after critical illness.损伤相关和病原体相关分子模式在危重病后晚期死亡率中发挥不同作用。
JCI Insight. 2019 Aug 22;4(16):127925. doi: 10.1172/jci.insight.127925.
5
Volatile anesthetics affect macrophage phagocytosis.挥发性麻醉剂会影响巨噬细胞的吞噬作用。
PLoS One. 2019 May 9;14(5):e0216163. doi: 10.1371/journal.pone.0216163. eCollection 2019.
6
Volatile Anesthetic Attenuates Phagocyte Function and Worsens Bacterial Loads in Wounds.挥发性麻醉剂可减弱吞噬细胞功能,并使伤口细菌负荷恶化。
J Surg Res. 2019 Jan;233:323-330. doi: 10.1016/j.jss.2018.07.075. Epub 2018 Sep 5.
7
Structural basis for species-specific activation of mouse Toll-like receptor 9.鼠 Toll 样受体 9 种属特异性激活的结构基础。
FEBS Lett. 2018 Aug;592(15):2636-2646. doi: 10.1002/1873-3468.13176. Epub 2018 Jul 13.
8
The source of cell-free mitochondrial DNA in trauma and potential therapeutic strategies.创伤中游离线粒体DNA的来源及潜在治疗策略。
Eur J Trauma Emerg Surg. 2018 Jun;44(3):325-334. doi: 10.1007/s00068-018-0954-3. Epub 2018 Apr 9.
9
Toll-like Receptor 9 Contains Two DNA Binding Sites that Function Cooperatively to Promote Receptor Dimerization and Activation.Toll 样受体 9 包含两个 DNA 结合位点,这些结合位点协同作用促进受体二聚化和激活。
Immunity. 2018 Apr 17;48(4):649-658.e4. doi: 10.1016/j.immuni.2018.03.013. Epub 2018 Apr 3.
10
Mitochondrial DAMPs Are Released During Cardiopulmonary Bypass Surgery and Are Associated With Postoperative Atrial Fibrillation.线粒体损伤相关分子模式在体外循环手术期间释放,并与术后房颤有关。
Heart Lung Circ. 2018 Jan;27(1):122-129. doi: 10.1016/j.hlc.2017.02.014. Epub 2017 Mar 24.

麻醉剂对 Toll 样受体 9 的影响。

The effect of anesthetics on toll like receptor 9.

机构信息

Department of Anesthesiology, Critical Care and Pain Medicine, Cardiac Anesthesia Division, Boston Children's Hospital, Boston, MA, USA.

Department of Anaesthesia, Harvard Medical School, Boston, MA, USA.

出版信息

FASEB J. 2020 Nov;34(11):14645-14654. doi: 10.1096/fj.202000791RR. Epub 2020 Sep 9.

DOI:10.1096/fj.202000791RR
PMID:32901993
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7814252/
Abstract

Toll like receptors (TLRs) are critical receptors to respond to danger signals, and their functions are relevant in the perioperative period. We previously reported that volatile anesthetics directly bound to TLR2 and TLR4 and attenuated their functions. Given that TLR9 can respond to mitochondrial DNA, a danger signal that is released upon tissue injury, we examined the role of anesthetics on TLR9 function. Our reporter assay showed that volatile anesthetics isoflurane and sevoflurane increased the activation of TLR9, while propofol attenuated it. TLR9 activation occurs via its dimerization. The dimerization is facilitated by unmethylated cytosine-phosphate-guanine (CpG) DNA as well as DNA containing cytosine at the second position from 5'-end (5'-xCx DNA). Our structural analysis using photoactivable anesthetics and rigid docking simulation showed that isoflurane and sevoflurane bound to both TLR9 dimer interface and 5'-xCx DNA binding site. Propofol bound to the TLR9 antagonist binding site. This is the first illustration that anesthetics can affect the binding of nucleic acids to their receptor. This study sets the foundation for the effect of anesthetics on TLR9 and will pave the way for future studies to determine the significance of such interactions in the clinical setting.

摘要

Toll 样受体 (TLRs) 是对危险信号做出反应的关键受体,其功能在围手术期具有重要意义。我们之前报道过挥发性麻醉剂可直接与 TLR2 和 TLR4 结合并减弱其功能。鉴于 TLR9 可以对线粒体 DNA 做出反应,线粒体 DNA 是组织损伤时释放的危险信号,我们研究了麻醉剂对 TLR9 功能的作用。我们的报告基因检测表明,挥发性麻醉剂异氟烷和七氟烷增加了 TLR9 的激活,而丙泊酚则减弱了其激活。TLR9 的激活是通过其二聚化来实现的。未甲基化的胞嘧啶-磷酸-鸟嘌呤(CpG)DNA 以及 5'端第二位为胞嘧啶的 DNA(5'-xCx DNA)有助于二聚化。我们使用光活化麻醉剂和刚性对接模拟的结构分析表明,异氟烷和七氟烷结合到 TLR9 二聚体界面和 5'-xCx DNA 结合位点。丙泊酚结合到 TLR9 拮抗剂结合位点。这是首次表明麻醉剂可以影响核酸与其受体的结合。本研究为麻醉剂对 TLR9 的影响奠定了基础,并为未来研究确定此类相互作用在临床环境中的意义铺平了道路。