Analysis of Signaling Pathways of Necroptotic and Pyroptotic Cell Death in the Hearts of Rats With Type 2 Diabetes Mellitus
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články
PubMed
37294115
PubMed Central
PMC10292816
DOI
10.33549/physiolres.935020
PII: 935020
Knihovny.cz E-zdroje
- MeSH
- apoptóza MeSH
- diabetes mellitus 2. typu * MeSH
- krysa rodu Rattus MeSH
- nekróza MeSH
- potkani Zucker MeSH
- proteinkinasy metabolismus MeSH
- pyroptóza * MeSH
- signální transdukce MeSH
- zánět MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- proteinkinasy MeSH
Diabetes mellitus is known to produce various cell-damaging events and thereby underlie heart dysfunction and remodeling. However, very little is known about its inflammation-associated pathomechanisms due to necrosis-like cell death. For this purpose, we aimed to investigate signaling pathways of necroptosis and pyroptosis, known to produce plasma membrane rupture with the resultant promotion of inflammation. One-year old Zucker diabetic fatty (ZDF) rats did not exhibit significant heart dysfunction as revealed by echocardiographic measurement. On the other hand, there was a decrease in heart rate due to diabetes. Immunoblotting analysis showed that the left ventricles of ZDF rats overexpress neither the main necroptotic proteins including receptor-interacting protein kinase 3 (RIP3) and mixed lineage domain kinase-like pseudokinase (MLKL), nor the pyroptotic regulators including NLR family pyrin domain containing 3 protein (NLRP3), caspase-1, interleukin-1 beta (IL-1beta and the N-terminal gasdermin D (GSDMD-N). On the other hand, the increased activation of the RIP3 kinase due to phosphorylation was found in such hearts. In summary, we showed for the first time that the activation of cardiac RIP3 is upregulated due to disturbances in glucose metabolism which, however, did not proceed to necrosis-like cell death. These data can indicate that the activated RIP3 might also underlie other pleiotropic, non-necroptotic signaling pathways under basal conditions.
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Adameova A, Hrdlicka J, Szobi A, Farkasova V, Kopaskova K, Murarikova M, Neckar J, Kolar F, Ravingerova T, Dhalla NS. Evidence of necroptosis in hearts subjected to various forms of ischemic insults. Can J Physiol Pharmacol. 2017;95:1163–1169. doi: 10.1139/cjpp-2016-0609. PubMed DOI
Chai R, Xue W, Shi S, Zhou Y, Du Y, Li Y, Song Q, Wu H, Hu Y. Cardiac remodeling in heart failure: Role of pyroptosis and its therapeutic implications. Front Cardiovasc Med. 2022;9:870924. doi: 10.3389/fcvm.2022.870924. PubMed DOI PMC
Patel P, Karch J. Regulation of cell death in the cardiovascular system. Int Rev Cell Mol Biol. 2020;353:153–09. doi: 10.1016/bs.ircmb.2019.11.005. PubMed DOI
Morgan MJ, Liu Z-G. Programmed cell death with a necrotic-like phenotype. Biomol Concepts. 2013;4:259–75. doi: 10.1515/bmc-2012-0056. PubMed DOI
Zhe-Wei S, Li-Sha G, Yue-Chun L. The role of necroptosis in cardiovascular disease. Front Pharmacol. 2018;9:721. doi: 10.3389/fphar.2018.00721. PubMed DOI PMC
Wang H, Sun L, Su L, Rizo J, Liu L, Wang LF, Wang FS, Wang X. Mixed lineage kinase domain-like protein MLKL causes necrotic membrane disruption upon phosphorylation by RIP3. Mol Cell. 2014;54:133–146. doi: 10.1016/j.molcel.2014.03.003. PubMed DOI
Wu XN, Yang ZH, Wang XK, Zhang Y, Wan H, Song Y, Chen X, Shao J, Han J. Distinct roles of RIP1–RIP3 hetero- and RIP3–RIP3 homo-interaction in mediating necroptosis. Cell Death Differ. 2014;21:1709–1720. doi: 10.1038/cdd.2014.77. PubMed DOI PMC
Dondelinger Y, Declercq W, Montessuit S, Roelandt R, Goncalves A, Bruggeman I, Hulpiau P, et al. MLKL compromises plasma membrane integrity by binding to phosphatidylinositol phosphates. Cell Rep. 2014;7:971–981. doi: 10.1016/j.celrep.2014.04.026. PubMed DOI
Liu X, Zhang Z, Ruan J, Pan Y, Magupalli VG, Wu H, Lieberman J. Inflammasome-activated gasdermin D causes pyroptosis by forming membrane pores. Nature. 2016;535:153–158. doi: 10.1038/nature18629. PubMed DOI PMC
Wang Q, Wu J, Zeng Y, Chen K, Wang C, Yang S, Sun N, Chen H, Duan K, Zeng G. Pyroptosis: A pro-inflammatory type of cell death in cardiovascular disease. Clin Chim Acta. 2020;510:62–2. doi: 10.1016/j.cca.2020.06.044. PubMed DOI
Del Re DP, Amgalan D, Linkermann A, Liu Q, Kitsis RN. Fundamental mechanisms of regulated cell death and implications for heart disease. Physiol Rev. 2019;99:1765–1817. doi: 10.1152/physrev.00022.2018. PubMed DOI PMC
Lichý M, Szobi A, Hrdlička J, Horváth C, Kormanová V, Rajtík T, Neckář J, Kolář F, Adameová A. Different signalling in infarcted and non-infarcted areas of rat failing hearts: A role of necroptosis and inflammation. J Cell Mol Med. 2019;23:6429–6441. doi: 10.1111/jcmm.14536. PubMed DOI PMC
Lawlor KE, Khan N, Mildenhall A, Gerlic M, Croker BA, D'Cruz AA, Hall C, et al. RIPK3 promotes cell death and NLRP3 inflammasome activation in the absence of MLKL. Nat Commun. 2015;6:6282. doi: 10.1038/ncomms7282. PubMed DOI PMC
Belke DD, Dillmann WH. Altered cardiac calcium handling in diabetes. Curr Hypertens Rep. 2004;6:424–429. doi: 10.1007/s11906-004-0035-3. PubMed DOI
Ravingerová T, Stetka R, Pancza D, Ulicná O, Ziegelhöffer A, Styk J. Susceptibility to ischemia-induced arrhythmias and the effect of preconditioning in the diabetic rat heart. Physiol Res. 2000;49:607–616. PubMed
Giacco F, Brownlee M, Schmidt AM. Oxidative stress and diabetic complications. Circ Res. 2010;107:1058–1070. doi: 10.1161/CIRCRESAHA.110.223545. PubMed DOI PMC
Kancirová I, Jašová M, Muráriková M, Sumbalová Z, Uličná O, Ravingerová T, Waczulíková I, Ziegelhöffer A, Ferko M. Cardioprotection induced by remote ischemic preconditioning preserves the mitochondrial respiratory function in acute diabetic myocardium. Physiol Res. 2016;65(Suppl 5):S611–S619. doi: 10.33549/physiolres.933533. PubMed DOI
Ahmed N, Babaei-Jadidi R, Howell SK, Beisswenger PJ, Thornalley PJ. Degradation products of proteins damaged by glycation, oxidation and nitration in clinical type 1 diabetes. Diabetologia. 2005;48:1590–1603. doi: 10.1007/s00125-005-1810-7. PubMed DOI
Tsalamandris S, Antonopoulos AS, Oikonomou E, Papamikroulis GA, Vogiatzi G, Papaioannou S, Deftereos S, Tousoulis D. The role of inflammation in diabetes: current concepts and future perspectives. Eur Cardiol. 2019;14:50–59. doi: 10.15420/ecr.2018.33.1. PubMed DOI PMC
Horvath C, Young M, Jarabicova I, Kindernay L, Ferenczyova K, Ravingerova T, Lewis M, Suleiman MS, Adameova A. Inhibition of cardiac RIP3 mitigates early reperfusion injury and calcium-induced mitochondrial swelling without altering necroptotic signalling. Int J Mol Sci. 2021;22:7983. doi: 10.3390/ijms22157983. PubMed DOI PMC
Jarabicová I, Horváth C, Vel’asová E, Bies Piváčková L, Vetešková J, Klimas J, Křenek P, Adameová A. Analysis of necroptosis and its association with pyroptosis in organ damage in experimental pulmonary arterial hypertension. J Cell Mol Med. 2022;26:2633–645. doi: 10.1111/jcmm.17272. PubMed DOI PMC
Moritz CP. Tubulin or not tubulin: Heading toward total protein staining as loading control in Western blots. Proteomics. 2017;17:201600189. doi: 10.1002/pmic.201600189. PubMed DOI
Liu Y, Liu T, Lei T, Zhang D, Du S, Girani L, Qi D, Lin C, Tong R, Wang Y. RIP1/RIP3-regulated necroptosis as a target for multifaceted disease therapy (Review) Int J Mol Med. 2019;44:771–786. doi: 10.3892/ijmm.2019.4244. PubMed DOI PMC
Jinawong K, Apaijai N, Wongsuchai S, Pratchayasakul W, Chattipakorn N, Chattipakorn SC. Necrostatin-1 mitigates cognitive dysfunction in prediabetic rats with no alteration in insulin sensitivity. Diabetes. 2020;69:1411–1423. doi: 10.2337/db19-1128. PubMed DOI
Xu H, Du X, Liu G, Huang S, Du W, Zou S, Tang D, et al. The pseudokinase MLKL regulates hepatic insulin sensitivity independently of inflammation. Mol Metab. 2019;23:14–3. doi: 10.1016/j.molmet.2019.02.003. PubMed DOI PMC
Lau H, Corrales N, Alexander M, Mohammadi MR, Li S, Smink AM, de Vos P, Lakey JRT. Necrostatin-1 supplementation enhances young porcine islet maturation and in vitro function. Xenotransplantation. 2020;27:e12555. doi: 10.1111/xen.12555. PubMed DOI
Cao T, Ni R, Ding W, Ji X, Li L, Liao G, Lu Y, Fan G-C, Zhang Z, Peng T. MLKL-mediated necroptosis is a target for cardiac protection in mouse models of type-1 diabetes. Cardiovasc Diabetol. 2022;21:165. doi: 10.1186/s12933-022-01602-9. PubMed DOI PMC
Qiao S, Hong L, Zhu Y, Zha J, Wang A, Qiu J, Li W, Wang C, An J, Zhang H. RIPK1–RIPK3 mediates myocardial fibrosis in type 2 diabetes mellitus by impairing autophagic flux of cardiac fibroblasts. Cell Death Dis. 2022;13:147. doi: 10.1038/s41419-022-04587-1. PubMed DOI PMC
Giricz Z, Koncsos G, Rajtík T, Varga ZV, Baranyai T, Csonka C, Szobi A, Adameová A, Gottlieb RA, Ferdinandy P. Hypercholesterolemia downregulates autophagy in the rat heart. Lipids Health Dis. 2017;16:60. doi: 10.1186/s12944-017-0455-0. PubMed DOI PMC
Luo B, Li B, Wang W, Liu X, Xia Y, Zhang C, Zhang M, Zhang Y, An F. NLRP3 gene silencing ameliorates diabetic cardiomyopathy in a type 2 diabetes rat model. PLoS One. 2014;19(9):e104771. doi: 10.1371/journal.pone.0104771. PubMed DOI PMC
Yang F, Qin Y, Wang Y, Meng S, Xian H, Che H, Lv J, et al. Metformin inhibits the NLRP3 inflammasome via AMPK/mTOR-dependent effects in diabetic cardiomyopathy. Int J Biol Sci. 2019;15:1010–1019. doi: 10.7150/ijbs.29680. PubMed DOI PMC
Sun Y, Ding S. NLRP3 Inflammasome in diabetic cardiomyopathy and exercise intervention. Int J Mol Sci. 2021;22:1322. doi: 10.3390/ijms222413228. PubMed DOI PMC
Zhang DW, Shao J, Lin J, Zhang N, Lu BJ, Lin SC, Dong MQ, Han J. RIP3, an energy metabolism regulator that switches TNF-induced cell death from apoptosis to necrosis. Science. 2009;325:332–36. doi: 10.1126/science.1172308. PubMed DOI
Yang Z, Wang Y, Zhang Y, He X, Zhong CQ, Ni H, Chen X, Liang Y, Wu J, Zhao S, Zhou D, Han J. RIP3 targets pyruvate dehydrogenase complex to increase aerobic respiration in TNF-induced necroptosis. Nat Cell Biol. 2018;20:186–197. doi: 10.1038/s41556-017-0022-y. PubMed DOI
Heat Stroke Induces Pyroptosis in Spermatogonia via the cGAS-STING Signaling Pathway