TY - JOUR
T1 - The effect of anesthetics on toll like receptor 9
AU - Koutsogiannaki, Sophia
AU - Bu, Weiming
AU - Hou, Lifei
AU - Shibamura-Fujiogi, Miho
AU - Ishida, Hanako
AU - Ohto, Umeharu
AU - Eckenhoff, Roderic G.
AU - Yuki, Koichi
N1 - Funding Information:
This work was in part supported by CHMC Anesthesia Foundation (KY) and NIH R01GM118277 (KY) and R01GM127600 (KY).
Publisher Copyright:
© 2020 Federation of American Societies for Experimental Biology
PY - 2020/11/1
Y1 - 2020/11/1
N2 - 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.
AB - 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.
KW - electrostatic potential
KW - nucleic acid
KW - toll-like receptor
KW - volatile anesthetics
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U2 - 10.1096/fj.202000791RR
DO - 10.1096/fj.202000791RR
M3 - Article
C2 - 32901993
AN - SCOPUS:85090430309
SN - 0892-6638
VL - 34
SP - 14645
EP - 14654
JO - FASEB Journal
JF - FASEB Journal
IS - 11
ER -