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