ALKBH3 suppresses ischemia/reperfusion-induced PANoptosis by regulating the ZBED6/STAT1/AIM2 axis through m1A demethylation

Hongtao Diao , Chunlei Wang , Yuting Xiong , Qiaoyue Zhao , Xinyue Zhang , Xiaohui Qi , Yuan Zou , Jiaxuan Li , Linghua Zeng , Wei Si , Feng Zhang , Ping Pang , Ning Wang , Yu Bian , Baofeng Yang

Clinical and Translational Medicine ›› 2026, Vol. 16 ›› Issue (3) : e70632

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Clinical and Translational Medicine ›› 2026, Vol. 16 ›› Issue (3) :e70632 DOI: 10.1002/ctm2.70632
RESEARCH ARTICLE
ALKBH3 suppresses ischemia/reperfusion-induced PANoptosis by regulating the ZBED6/STAT1/AIM2 axis through m1A demethylation
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Abstract

Background: Myocardial ischemia/reperfusion (I/R) injury induces an intense inflammatory response and involves multiple cell death pathways. PANoptosis, an integrated cell death process involving pyroptosis, apoptosis and necroptosis, is a major driver of cardiomyocyte loss during I/R injury. However, the epitranscriptomic control of PANoptosis is poorly understood.

Methods: We investigated the role of ALKBH3, an mRNA N1-methyladenosine (m1A) demethylase, in the regulation of cardiomyocyte PANoptosis using hypoxia/reoxygenation models in vitro and murine I/R models in vivo. Integrated transcriptomic and m1A epitranscriptomic profiling identified downstream targets. Loss- and gain-of-function studies of ALKBH3, AIM2, ZBED6 and STAT1 (siRNA or plasmid overexpression) were coupled with assessments of cell death phenotypes, inflammasome activity and gene expression. Molecular interactions and transcriptional/translational regulation were examined using co-immunoprecipitation, chromatin immunoprecipitation (ChIP) and dual-luciferase reporter assays.

Results: Cardiomyocyte-restricted ALKBH3 overexpression mitigates I/R injury in vivo. Mechanistically, ALKBH3 acts as a key suppressor of PANoptosis by inhibiting AIM2. ALKBH3 demethylates m1A onZBED6 mRNA, enhancing ZBED6 translation and limiting cardiomyocyte PANoptosis. Although ZBED6 does not bind directly to the AIM2 promoter, it physically interacts with STAT1, a transcriptional activator of AIM2, and represses STAT1-driven AIM2 expression. ZBED6 overexpression reduces AIM2 levels and PANoptosis, whereas AIM2 knockout attenuates the exacerbation of cardiac injury and PANoptosis induced by ALKBH3 silencing.

Conclusions: These findings identify the ALKBH3/ZBED6/STAT1/AIM2 signalling axis that epitranscriptomically breaks cardiomyocyte PANoptosis, highlighting a tractable therapeutic target that limits cell death and improves myocardial outcomes after I/R.

Keywords

AIM2 / ALKBH3 / m1A modification / PANoptosis

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Hongtao Diao, Chunlei Wang, Yuting Xiong, Qiaoyue Zhao, Xinyue Zhang, Xiaohui Qi, Yuan Zou, Jiaxuan Li, Linghua Zeng, Wei Si, Feng Zhang, Ping Pang, Ning Wang, Yu Bian, Baofeng Yang. ALKBH3 suppresses ischemia/reperfusion-induced PANoptosis by regulating the ZBED6/STAT1/AIM2 axis through m1A demethylation. Clinical and Translational Medicine, 2026, 16 (3) : e70632 DOI:10.1002/ctm2.70632

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References

[1]

Sicklinger F, Hartmann N, Kovacs A, et al. High-throughput echocardiography-guided induction of myocardial ischemia/reperfusion in mice. Circ Res. 2025; 136(10): 1099-1109.

[2]

Long Q, Rabi K, Cai Y, et al. Identification of splenic IRF7 as a nanotherapy target for tele-conditioning myocardial reperfusion injury. Nat Commun. 2025; 16: 1909.

[3]

Hofmann C, Serafin A, Schwerdt OM, et al. Transient inhibition of translation improves cardiac function after ischemia/reperfusion by attenuating the inflammatory response. Circulation. 2024; 150: 1248-1267.

[4]

Luo Q, Li Z, Sun W, et al. Myocardia-injected synergistically anti-apoptotic and anti-inflammatory poly(amino acid) hydrogel relieves ischemia-reperfusion injury. Adv Mater. 2025; 37:e2420171.

[5]

Chen C, Ma J, Duan S, et al. Mitigation of ischemia/reperfusion injury via selenium nanoparticles: suppression of STAT1 to inhibit cardiomyocyte oxidative stress and inflammation. Biomaterials. 2025; 318:123119.

[6]

Lambert JP, Luongo TS, Tomar D, et al. MCUB regulates the molecular composition of the mitochondrial calcium uniporter channel to limit mitochondrial calcium overload during stress. Circulation. 2019; 140: 1720-1733.

[7]

Joiner ML, Koval OM, Li J, et al. CaMKII determines mitochondrial stress responses in heart. Nature. 2012; 491: 269-273.

[8]

Mendoza A, Patel P, Robichaux D, Ramirez D, Karch J. Inhibition of the mPTP and lipid peroxidation is additively protective against I/R injury. Circ Res. 2024; 134: 1292-1305.

[9]

Kirshenbaum LA, Dhingra R, Bravo-Sagua R, Lavandero S. DIAPH1-MFN2 interaction decreases the endoplasmic reticulum-mitochondrial distance and promotes cardiac injury following myocardial ischemia. Nat Commun. 2024; 15: 1469.

[10]

Du B, Fu Q, Yang Q, et al. Different types of cell death and their interactions in myocardial ischemia-reperfusion injury. Cell Death Discov. 2025; 11: 87.

[11]

Tsurusaki S, Kizana E. Mechanisms and therapeutic potential of multiple forms of cell death in myocardial ischemia-reperfusion injury. Int J Mol Sci. 2024; 25(24):13492.

[12]

Mastoor Y, Murphy E, Roman B. Mechanisms of postischemic cardiac death and protection following myocardial injury. J Clin Invest. 2025; 135(1):e184134.

[13]

Li Y, Jin H, Li Q, Shi L, Mao Y, Zhao L. The role of RNA methylation in tumor immunity and its potential in immunotherapy. Mol Cancer. 2024; 23: 130.

[14]

Dominissini D, Nachtergaele S, Moshitch-Moshkovitz S, et al. The dynamic N(1)-methyladenosine methylome in eukaryotic messenger RNA. Nature. 2016; 530: 441-446.

[15]

Deng Y, Chen Z, Chen P, et al. ALKBH3-regulated m(1)A of ALDOA potentiates glycolysis and doxorubicin resistance of triple negative breast cancer cells. Acta Pharm Sin B. 2025; 15: 3092-3106.

[16]

Tu L, Gu S, Xu R, et al. ALKBH3-mediated M(1)A demethylation of METTL3 endows pathological fibrosis:interplay between M(1)A and M(6)A RNA methylation. Adv Sci (Weinh). 2025; 12(19):e2417067.

[17]

Sun H, Li K, Liu C, Yi C. Regulation and functions of non-m(6)A mRNA modifications. Nat Rev Mol Cell Biol. 2023; 24: 714-731.

[18]

Gu X, Zhuang A, Yu J, et al. Histone lactylation-boosted ALKBH3 potentiates tumor progression and diminished promyelocytic leukemia protein nuclear condensates by m1A demethylation of SP100A. Nucleic Acids Res. 2024; 52: 2273-2289.

[19]

Safra M, Sas-Chen A, Nir R, et al. The m1A landscape on cytosolic and mitochondrial mRNA at single-base resolution. Nature. 2017; 551: 251-255.

[20]

Smoczynski J, Yared MJ, Meynier V, Barraud P, Tisne C. Advances in the structural and functional understanding of m(1)A RNA modification. Acc Chem Res. 2024; 57: 429-438.

[21]

Wang X, Ma X, Chen S, et al. Harnessing m1A modification: a new frontier in cancer immunotherapy. Front Immunol. 2024; 15:1517604.

[22]

Wang H, Xie L, Guo H, et al. m(1)A demethylase Alkbh3 regulates neurogenesis through m(1)A demethylation of Mmp15 mRNA. Cell Biosci. 2024; 14: 92.

[23]

Ding YP, Liu CC, Yu KD. RNA modifications in the tumor microenvironment: insights into the cancer-immunity cycle and beyond. Exp Hematol Oncol. 2025; 14: 48.

[24]

Cui L, Ma R, Cai J, et al. RNA modifications: importance in immune cell biology and related diseases. Signal Transduct Target Ther. 2022; 7: 334.

[25]

Wu Y, Zhan S, Xu Y, Gao X. RNA modifications in cardiovascular diseases, the potential therapeutic targets. Life Sci. 2021; 278:119565.

[26]

Zhang G, Wang X, Li C, et al. Integrated stress response couples mitochondrial protein translation with oxidative stress control. Circulation. 2021; 144: 1500-1515.

[27]

Zhang L, Duan HC, Paduch M, et al. The molecular basis of human ALKBH3 mediated RNA N(1)-methyladenosine (m(1) A) demethylation. Angew Chem Int Ed Engl. 2024; 63:e202313900.

[28]

Cheng W, Ma J, Tao Q, et al. Demethylation of m1A assisted degradation of the signal probe for rapid electrochemical detection of ALKBH3 activity with practical applications. Talanta. 2022; 240:123151.

[29]

Wu Y, Chen Z, Xie G, et al. RNA m(1)A methylation regulates glycolysis of cancer cells through modulating ATP5D. Proc Natl Acad Sci USA. 2022; 119:e2119038119.

[30]

Bei Y, Zhu Y, Zhou J, et al. Inhibition of Hmbox1 promotes cardiomyocyte survival and glucose metabolism through Gck activation in ischemia/reperfusion injury. Circulation. 2024; 150: 848-866.

[31]

Qu Z, Pang X, Mei Z, et al. The positive feedback loop of the NAT10/Mybbp1a/p53 axis promotes cardiomyocyte ferroptosis to exacerbate cardiac I/R injury. Redox Biol. 2024; 72:103145.

[32]

Zhao M, Zheng Z, Liu J, et al. LGR6 protects against myocardial ischemia-reperfusion injury via suppressing necroptosis. Redox Biol. 2024; 78:103400.

[33]

Wang K, Li FH, Zhou LY, et al. HNEAP regulates necroptosis of cardiomyocytes by suppressing the m(5) C methylation of Atf7 mRNA. Adv Sci (Weinh). 2023; 10:e2304329.

[34]

Duan Y, Li Q, Wu J, et al. A detrimental role of endothelial S1PR2 in cardiac ischemia-reperfusion injury via modulating mitochondrial dysfunction, NLRP3 inflammasome activation, and pyroptosis. Redox Biol. 2024; 75:103244.

[35]

Shi H, Gao Y, Dong Z, et al. GSDMD-mediated cardiomyocyte pyroptosis promotes myocardial I/R injury. Circ Res. 2021; 129: 383-396.

[36]

Liu S, Bi Y, Han T, et al. The E3 ubiquitin ligase MARCH2 protects against myocardial ischemia-reperfusion injury through inhibiting pyroptosis via negative regulation of PGAM5/MAVS/NLRP3 axis. Cell Discov. 2024; 10: 24.

[37]

Ma XH, Liu JH, Liu CY, et al. ALOX15-launched PUFA-phospholipids peroxidation increases the susceptibility of ferroptosis in ischemia-induced myocardial damage. Signal Transduct Target Ther. 2022; 7: 288.

[38]

Cai W, Liu L, Shi X, et al. Alox15/15-HpETE aggravates myocardial ischemia-reperfusion injury by promoting cardiomyocyte ferroptosis. Circulation. 2023; 147: 1444-1460.

[39]

Wang Y, Song Y, Xu L, et al. A membrane-targeting aggregation-induced emission probe for monitoring lipid droplet dynamics in ischemia/reperfusion-induced cardiomyocyte ferroptosis. Adv Sci (Weinh). 2024; 11:e2309907.

[40]

Zhu L, Liu Y, Wang K, Wang N. Regulated cell death in acute myocardial infarction: molecular mechanisms and therapeutic implications. Ageing Res Rev. 2025; 104:102629.

[41]

Zhang X, Tang B, Luo J, et al. Cuproptosis, ferroptosis and PANoptosis in tumor immune microenvironment remodeling and immunotherapy: culprits or new hope. Mol Cancer. 2024; 23: 255.

[42]

Sundaram B, Pandian N, Mall R, et al. NLRP12-PANoptosome activates PANoptosis and pathology in response to heme and PAMPs. Cell. 2023; 186: 2783-2801.e2720.

[43]

Sundaram B, Pandian N, Kim HJ, et al. NLRC5 senses NAD(+) depletion, forming a PANoptosome and driving PANoptosis and inflammation. Cell. 2024; 187: 4061-4077.e4017.

[44]

Li PB, Bai JQ, Jiang WX, Li HH, Li CM. The mechanosensitive Piezo1 channel exacerbates myocardial ischaemia/reperfusion injury by activating caspase-8-mediated PANoptosis. Int Immunopharmacol. 2024; 139:112664.

[45]

Cui B, Qi Z, Liu W, Zhang G, Lin D. ZBP1-mediated PANoptosis: a possible novel mechanism underlying the therapeutic effects of penehyclidine hydrochloride on myocardial ischemia-reperfusion injury. Int Immunopharmacol. 2024; 137:112373.

[46]

Chen Y, Guan B, Lu J, et al. Gypensapogenin I alleviates PANoptosis, ferroptosis, and oxidative stress in myocardial ischemic-reperfusion injury by targeting the NOX2/AMPK pathway. Front Cell Dev Biol. 2025; 13:1623846.

[47]

Lee S, Karki R, Wang Y, Nguyen LN, Kalathur RC, Kanneganti TD. AIM2 forms a complex with pyrin and ZBP1 to drive PANoptosis and host defence. Nature. 2021; 597: 415-419.

[48]

Fidler TP, Xue C, Yalcinkaya M, et al. The AIM2 inflammasome exacerbates atherosclerosis in clonal haematopoiesis. Nature. 2021; 592: 296-301.

[49]

Wu L, Su J, Cao Y, et al. Dual-targeting nuclear and mitochondrial DNA damage drives immunogenic activation via PANoptosis for synergistic magneto-thermodynamic-chemotherapy. Biomaterials. 2026; 329:123924.

[50]

Onodi Z, Ruppert M, Kucsera D, et al. AIM2-driven inflammasome activation in heart failure. Cardiovasc Res. 2021; 117: 2639-2651.

[51]

Mao H, Angelini A, Li S, et al. CRAT links cholesterol metabolism to innate immune responses in the heart. Nat Metab. 2023; 5: 1382-1394.

[52]

Li X, Xiong X, Wang K, et al. Transcriptome-wide mapping reveals reversible and dynamic N(1)-methyladenosine methylome. Nat Chem Biol. 2016; 12: 311-316.

[53]

Christgen S, Zheng M, Kesavardhana S, et al. Identification of the PANoptosome: a molecular platform triggering pyroptosis, apoptosis, and necroptosis (PANoptosis). Front Cell Infect Microbiol. 2020; 10: 237.

[54]

Wang Z, Yang Y, Yao FT, et al. KLX ameliorates liver cancer progression by mediating ZBP1 transcription and ubiquitination and increasing ZBP1-induced PANoptosis. Acta Pharmacol Sin. 2025; 46: 2282-2295.

[55]

Zhang Z, Zhang F, Pang P, et al. Identification of PANoptosis-relevant subgroups to evaluate the prognosis and immune landscape of patients with liver hepatocellular carcinoma. Front Cell Dev Biol. 2023; 11:1210456.

[56]

Zhang M, Zhao X, Cai T, Wang F. PANoptosis: potential new targets and therapeutic prospects in digestive diseases. Apoptosis. 2025; 30: 2745-2760.

[57]

Upmanyu K, Upadhyay S. Wiring and rewiring PANoptosis: molecular vulnerabilities for targeting inflammatory cell death in human disease. Cytokine Growth Factor Rev. 2025; 86: 1-16.

[58]

Pandeya A, Kanneganti TD. Therapeutic potential of PANoptosis: innate sensors, inflammasomes, and RIPKs in PANoptosomes. Trends Mol Med. 2024; 30: 74-88.

[59]

Lin Q, Cai H, Yu F, et al. AIM2-PANoptosome-driven PANoptosis in hepatic lipid dysregulation induced by beta-HCH and nanoplastics co-exposure. Apoptosis. 2025; 30: 2340-2357.

[60]

Bai M, Lei J, Li F, et al. Short-chain chlorinated paraffins may induce ovarian damage in mice via AIM2- and NLRP12-PANoptosome. Environ Sci Technol. 2025; 59: 163-176.

[61]

Chen J, Tao Y, Wang Q, et al. AIM2 regulated by JAK3/STAT1 pathway promotes PANoptosis in intestinal barrier dysfunction caused by concomitant radiation and PD-1 blockade. Apoptosis. 2025; 30: 3009-3025.

[62]

Wu H, Jiang W, Pang P, et al. m(6)A reader YTHDF1 promotes cardiac fibrosis by enhancing AXL translation. Front Med. 2024; 18: 499-515.

[63]

Mohan M, Akula D, Dhillon A, Goyal A, Anindya R. Human RAD51 paralogue RAD51C fosters repair of alkylated DNA by interacting with the ALKBH3 demethylase. Nucleic Acids Res. 2019; 47: 11729-11745.

[64]

Monoe Y, Miyamoto S, Jingushi K, et al. Hypoxia regulates tumour characteristic RNA modifications in ovarian cancers. FEBS J. 2023; 290: 2085-2096.

[65]

Wu Y, Jiang D, Zhang H, et al. N1-methyladenosine (m1A) regulation associated with the pathogenesis of abdominal aortic aneurysm through YTHDF3 modulating macrophage polarization. Front Cardiovasc Med. 2022; 9:883155.

[66]

Liu Y, Zhang S, Gao X, Ru Y, Gu X, Hu X. Research progress of N1-methyladenosine RNA modification in cancer. Cell Commun Signal. 2024; 22: 79.

[67]

Duan J, Cao Z, Zhou Z, et al. Mitochondrial dysfunction drives ZBP1-mediated PANoptosis to increase the susceptibility of heart failure with preserved ejection fraction-associated atrial fibrillation. J Adv Res. 2025.

[68]

Xie Y, Shen A, Lin H, et al. Tetramethylpyrazine ameliorates 5-fluorouracil-Induced cardiotoxicity by inhibiting PANoptosis and suppressing the p38 MAPK/JNK/ERK signaling pathway. Eur J Pharmacol. 2025; 1006:178180.

[69]

Du L, Wang X, Chen S, Guo X. The AIM2 inflammasome: a novel biomarker and target in cardiovascular disease. Pharmacol Res. 2022; 186:106533.

[70]

Xu X, Wang Y, Pei K, et al. Shengmai-Yin resists myocardial ischemia reperfusion injury by inhibiting K27 ubiquitination of absent in melanoma 2. J Ethnopharmacol. 2025; 345:119553.

[71]

Zhang X, Song S, Huang Z, et al. Z-DNA-binding protein 1 exacerbates myocardial ischemia‒reperfusion injury by inducing noncanonical cardiomyocyte PANoptosis. Signal Transduct Target Ther. 2025; 10: 333.

[72]

Liu H, Pan D, Li P, et al. Loss of ZBED6 protects against sepsis-induced muscle atrophy by upregulating DOCK3-mediated RAC1/PI3K/AKT signaling pathway in pigs. Adv Sci (Weinh). 2023; 10:e2302298.

[73]

Younis S, Schonke M, Massart J, et al. The ZBED6-IGF2 axis has a major effect on growth of skeletal muscle and internal organs in placental mammals. Proc Natl Acad Sci U S A. 2018; 115: E2048-E2057.

[74]

Younis S, Naboulsi R, Wang X, et al. The importance of the ZBED6-IGF2 axis for metabolic regulation in mouse myoblast cells. FASEB J. 2020; 34: 10250-10266.

[75]

Lu C, Ma H, Song L, et al. IFN-gammaR/STAT1 signaling in recipient hematopoietic antigen-presenting cells suppresses graft-versus-host disease. J Clin Invest. 2023; 133(3):e125986.

[76]

Zeng G, Lian C, Yang P, Zheng M, Ren H, Wang H. E3-ubiquitin ligase TRIM6 aggravates myocardial ischemia/reperfusion injury via promoting STAT1-dependent cardiomyocyte apoptosis. Aging (Albany NY). 2019; 11: 3536-3550.

[77]

Shi X, Xu J, Liu L, et al. Deubiquitinase MYSM1 drives myocardial ischemia/reperfusion injury by stabilizing STAT1 in cardiomyocytes. Theranostics. 2025; 15: 1606-1621.

[78]

Zhang J, Xu Y, Wei C, et al. Macrophage neogenin deficiency exacerbates myocardial remodeling and inflammation after acute myocardial infarction through JAK1-STAT1 signaling. Cell Mol Life Sci. 2023; 80: 324.

[79]

Karki R, Sharma BR, Tuladhar S, et al. Synergism of TNF-alpha and IFN-gamma triggers inflammatory cell death, tissue damage, and mortality in SARS-CoV-2 infection and cytokine shock syndromes. Cell. 2021; 184: 149-168.e117.

[80]

Sharma BR, Karki R, Rajesh Y, Kanneganti TD. Immune regulator IRF1 contributes to ZBP1-, AIM2-, RIPK1-, and NLRP12-PANoptosome activation and inflammatory cell death (PANoptosis). J Biol Chem. 2023; 299:105141.

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2026 The Author(s). Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics.

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