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Macrophage-mediated IL-6 signaling drives ryanodine receptor-2 calcium leak in postoperative atrial fibrillation

Macrophage-mediated IL-6 signaling drives ryanodine receptor–2 calcium leak in postoperative atrial fibrillation Joshua A. Keefe, Yuriana Aguilar-Sanchez, J. Alberto Navarro-Garcia, Isabelle Ong, Luge Li, Amelie Paasche, Issam Abu-Taha, Marcel A. Tekook, Florian Bruns, Shuai Zhao, Markus Kamler, Yin...

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Main Authors: Keefe, Joshua Anthony (Author) , Aguilar-Sanchez, Yuriana (Author) , Navarro-Garcia, J. Alberto (Author) , Ong, Isabelle (Author) , Li, Luge (Author) , Paasche, Amelie (Author) , Abu-Taha, Issam (Author) , Tekook, Marcel A. (Author) , Bruns, Florian (Author) , Zhao, Shuai (Author) , Kamler, Markus (Author) , Shen, Ying H. (Author) , Chelu, Mihail G. (Author) , Li, Na (Author) , Dobrev, Dobromir (Author) , Wehrens, Xander H. T. (Author)
Format: Article (Journal)
Language:English
Published: March 6, 2025
In: The journal of clinical investigation
Year: 2025, Volume: 135, Issue: 9, Pages: 1-17
ISSN:1558-8238
DOI:10.1172/JCI187711
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1172/JCI187711
Verlag, kostenfrei, Volltext: https://www.jci.org/articles/view/187711
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Author Notes:Joshua A. Keefe, Yuriana Aguilar-Sanchez, J. Alberto Navarro-Garcia, Isabelle Ong, Luge Li, Amelie Paasche, Issam Abu-Taha, Marcel A. Tekook, Florian Bruns, Shuai Zhao, Markus Kamler, Ying H. Shen, Mihail G. Chelu, Na Li, Dobromir Dobrev, and Xander H.T. Wehrens
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Summary:Macrophage-mediated IL-6 signaling drives ryanodine receptor–2 calcium leak in postoperative atrial fibrillation Joshua A. Keefe, Yuriana Aguilar-Sanchez, J. Alberto Navarro-Garcia, Isabelle Ong, Luge Li, Amelie Paasche, Issam Abu-Taha, Marcel A. Tekook, Florian Bruns, Shuai Zhao, Markus Kamler, Ying H. Shen, Mihail G. Chelu, Na Li, Dobromir Dobrev, Xander H.T. WehrensJ Clin Invest. 2025;135(9):e187711. https://doi.org/10.1172/JCI187711. Postoperative atrial fibrillation (poAF) is AF occurring days after surgery, with a prevalence of 33% among patients undergoing open-heart surgery. The degree of postoperative inflammation correlates with poAF risk, but less is known about the cellular and molecular mechanisms driving postoperative atrial arrhythmogenesis. We performed single-cell RNA-seq comparing atrial nonmyocytes from mice with and without poAF, which revealed infiltrating CCR2+macrophages to be the most altered cell type. Pseudotime trajectory analyses identified Il-6 as a gene of interest driving in macrophages, which we confirmed in pericardial fluid collected from human patients after cardiac surgery. Indeed, macrophage depletion and macrophage-specific Il6ra conditional knockout (cKO) prevented poAF in mice. Downstream STAT3 inhibition with TTI-101 and cardiomyocyte-specific Stat3 cKO rescued poAF, indicating a proarrhythmogenic roleof STAT3 in poAF development. Confocal imaging in isolated atrial cardiomyocytes (ACMs) uncovered what we believe to be a novel link between STAT3 and CaMKII-mediated ryanodine receptor–2 (RyR2)-Ser(S)2814 phosphorylation. Indeed, nonphosphorylatable RyR2S2814A mice were protected from poAF, and CaMKII inhibition prevented arrhythmogenic Ca2+ mishandling in ACMs from mice with poAF. Altogether, we provide multiomic, biochemical, and functional evidence frommice and humans that IL-6-STAT3-CaMKII signaling driven by infiltrating atrial macrophages is a pivotal driver of poAF, which portends therapeutic utility for poAF prevention.
Item Description:Gesehen am 10.12.2025
Physical Description:Online Resource
ISSN:1558-8238
DOI:10.1172/JCI187711

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