This work is licensed under the Creative Commons Attribution 4.0 International License.
Yeh RW, Sidney S, Chandra M, Sorel M, Selby JV, Go AS. Population trends in the incidence and outcomes of acute myocardial infarction. N Engl J Med 2010;362: 2155–65.YehRWSidneySChandraMSorelMSelbyJVGoASPopulation trends in the incidence and outcomes of acute myocardial infarctionN Engl J Med201036221556510.1056/NEJMoa090861020558366Search in Google Scholar
Nielsen PH, Maeng M, Busk M, Mortensen LS, Kristensen SD, Nielsen TT, Andersen HR. Primary angioplasty versus fibrinolysis in acute myocardial infarction: long-term follow-up in the Danish acute myocardial infarction 2 trial. Circulation 2010;121: 1484–1491.NielsenPHMaengMBuskMMortensenLSKristensenSDNielsenTTAndersenHRPrimary angioplasty versus fibrinolysis in acute myocardial infarction: long-term follow-up in the Danish acute myocardial infarction 2 trialCirculation20101211484149110.1161/CIRCULATIONAHA.109.87322420308618Search in Google Scholar
Zhang J, Knapton A, Lipshultz SE, Weaver JL, Herman EH. Isoproterenol-induced cardiotoxicity in Sprague-Dawley rats: correlation of reversible and irreversible myocardial injury with release of cardiac troponin t and roles of inos in myocardial injury. Toxicol Pathol. 2008;36(2):277–78.ZhangJKnaptonALipshultzSEWeaverJLHermanEHIsoproterenol-induced cardiotoxicity in Sprague-Dawley rats: correlation of reversible and irreversible myocardial injury with release of cardiac troponin t and roles of inos in myocardial injuryToxicol Pathol.20083622777810.1177/019262330731301018349426Search in Google Scholar
Antonio EL, Dos Santos AA, Araujo SR, Bocalini DS, Dos Santos L, Fenelon G, Frnco MF, Tucci PJ. Left ventricle radio-frequency ablation in the rat: a new model of heart failure due to myocardial infarction homogeneous in size and low in mortality. J Card Fail. 2009;15(6): 540–548.AntonioELDos SantosAAAraujoSRBocaliniDSDos SantosLFenelonGFrncoMFTucciPJLeft ventricle radio-frequency ablation in the rat: a new model of heart failure due to myocardial infarction homogeneous in size and low in mortalityJ Card Fail.200915654054810.1016/j.cardfail.2009.01.00719643366Search in Google Scholar
Ovsepyan A, Panchenkov D, Prokhortchouk E, Telegin G, Zhigalova N, Golubev E, Sviridova T, Matskeplishvili S, Skryabin K, Buziashvili U. Modeling myocardial infarction in mice: methodology, monitoring, pathomorphology. Acta Naturae. 2011;3(1): 107–115.OvsepyanAPanchenkovDProkhortchoukETeleginGZhigalovaNGolubevESviridovaTMatskeplishviliSSkryabinKBuziashviliUModeling myocardial infarction in mice: methodology, monitoring, pathomorphologyActa Naturae.20113110711510.32607/20758251-2011-3-1-107-115Search in Google Scholar
Wang D, Tediashvili G, Hu X, Gravina A, Marcus SG, Zhang H, Olgin JE, Deuse T, Schrepfer S. A Cryoinjury Model to Study Myocardial Infarction in the Mouse. J Vis Exp 2019;151: 1–5.WangDTediashviliGHuXGravinaAMarcusSGZhangHOlginJEDeuseTSchrepferSA Cryoinjury Model to Study Myocardial Infarction in the MouseJ Vis Exp20191511510.3791/5995831609308Search in Google Scholar
Villiers CD, Riley PR. Mouse models of myocardial infarction: comparing permanent ligation and ischaemia-reperfusion. Disease Models & Mechanisms 2020; 13: 1–5.VilliersCDRileyPRMouse models of myocardial infarction: comparing permanent ligation and ischaemia-reperfusionDisease Models & Mechanisms2020131510.1242/dmm.046565768785933361140Search in Google Scholar
Johns TN, Olson BJ. Experimental myocardial infarction. I. A method of coronary occlusion in small animals. Ann Surg. 1954;140: 675–682.JohnsTNOlsonBJExperimental myocardial infarction. I. A method of coronary occlusion in small animalsAnn Surg.195414067568210.1097/00000658-195411000-00006160965013208115Search in Google Scholar
Gao E, Lei YH, Shang X, Huang ZM, Zuo L, Boucher M, Fan Q, Chuprun JK, Ma XL, Koch WJ. A novel and efficient model of coronary artery ligation and myocardial infarction in the mouse. Circ Res. 2010;107: 1445–1453.GaoELeiYHShangXHuangZMZuoLBoucherMFanQChuprunJKMaXLKochWJA novel and efficient model of coronary artery ligation and myocardial infarction in the mouseCirc Res.20101071445145310.1161/CIRCRESAHA.110.223925300581720966393Search in Google Scholar
Pruenster M, Vogl T, Roth J, Sperandio M. S100A8/A9: From basic science to clinical application. Pharmacol Ther. 2016;167: 120–131.PruensterMVoglTRothJSperandioMS100A8/A9: From basic science to clinical applicationPharmacol Ther.201616712013110.1016/j.pharmthera.2016.07.01527492899Search in Google Scholar
Marinkovic G, Larsen HG, Yndigegn T, Szabo IA, Mares RG, De Camp L, Weiland M, Tomas L, Goncalves I, Nilsson J, Jovinge S, Schiopu A. Inhibition of pro-inflammatory myeloid cell responses by short-term S100A9 blockade improves cardiac function after myocardial infarction. European Heart Journal 2019;40(32): 2713–2723.MarinkovicGLarsenHGYndigegnTSzaboIAMaresRGDe CampLWeilandMTomasLGoncalvesINilssonJJovingeSSchiopuAInhibition of pro-inflammatory myeloid cell responses by short-term S100A9 blockade improves cardiac function after myocardial infarctionEuropean Heart Journal201940322713272310.1093/eurheartj/ehz461Search in Google Scholar
Marinkovic G, Koenis DS, De Camp L, Jablonowski R, Graber N, De Waard V, Carlie De Vries CJ, Goncalves I, Nilsson J, Jovinge S, Schiopu A. S100A9 Links Inflammation and Repair in Myocardial Infarction. Circ Res. 2020;127(5): 664–676.MarinkovicGKoenisDSDe CampLJablonowskiRGraberNDe WaardVCarlie De VriesCJGoncalvesINilssonJJovingeSSchiopuAS100A9 Links Inflammation and Repair in Myocardial InfarctionCirc Res.2020127566467610.1161/CIRCRESAHA.120.315865Search in Google Scholar
Ruiz-Villalba A, Simon AM, Pogontke C, Castillo MI, Abizanda G, Pelacho, Sánchez-Domínguez BR, Segovia JC, Prósper F, Pérez-Pomares JM. Interacting resident epicardium-derived fibroblasts and recruited bone marrow cells form myocardial infarction scar. J Am Coll Cardiol. 2015;65: 2057–66.Ruiz-VillalbaASimonAMPogontkeCCastilloMIAbizandaGPelachoSánchez-DomínguezBRSegoviaJCPrósperFPérez-PomaresJMInteracting resident epicardium-derived fibroblasts and recruited bone marrow cells form myocardial infarction scarJ Am Coll Cardiol.20156520576610.1016/j.jacc.2015.03.520Search in Google Scholar
Ma Y, Yabluchanskiy A, Iyer RP, Cannon PL, Flynn ER, Jung M, Henry J, Cates CA, Deleon-Pennell KY, Lindsey ML. Temporal neutrophil polarization following myocardial infarction. Cardiovasc Res. 2016;110: 51–61.MaYYabluchanskiyAIyerRPCannonPLFlynnERJungMHenryJCatesCADeleon-PennellKYLindseyMLTemporal neutrophil polarization following myocardial infarctionCardiovasc Res.2016110516110.1093/cvr/cvw024Search in Google Scholar
Horckmans M, Ring L, Duchene J, Santovito D, Schloss MJ, Drechsler M, Weber C, Soehnlein O, Steffens S. Neutrophils orchestrate post-myocardial infarction healing by polarizing macrophages towards a reparative phenotype. Eur Heart J. 2017;38: 187–197.HorckmansMRingLDucheneJSantovitoDSchlossMJDrechslerMWeberCSoehnleinOSteffensSNeutrophils orchestrate post-myocardial infarction healing by polarizing macrophages towards a reparative phenotypeEur Heart J.20173818719710.1093/eurheartj/ehw002Search in Google Scholar
Geissmann F, Jung S, Littman DR. Blood monocytes consist of two principal subsets with distinct migratory properties. Immunity. 2003;19: 71–82.GeissmannFJungSLittmanDRBlood monocytes consist of two principal subsets with distinct migratory propertiesImmunity.200319718210.1016/S1074-7613(03)00174-2Search in Google Scholar
Epelman S, Lavine KJ, Beaudin AE, Sojka DK, Carrero JA, Calderon B, Brija T, Gautier EL, Ivanov S, Satpathy AT, Schilling JD, Schwendener R, Sergin I, Razani B, Forsberg EC, Yokoyama WM, Unanue ER, Colonna M, Randolph GJ, Mann DL. Embryonic and adult-derived resident cardiac macrophages are maintained through distinct mechanisms at steady state and during inflammation. Immunity. 2014;40: 91–104.EpelmanSLavineKJBeaudinAESojkaDKCarreroJACalderonBBrijaTGautierELIvanovSSatpathyATSchillingJDSchwendenerRSerginIRazaniBForsbergECYokoyamaWMUnanueERColonnaMRandolphGJMannDLEmbryonic and adult-derived resident cardiac macrophages are maintained through distinct mechanisms at steady state and during inflammationImmunity.2014409110410.1016/j.immuni.2013.11.019392330124439267Search in Google Scholar
Wan E, Yeap XY, Dehn S, Terry R, Novak M, Zhang S, Iwata S, Han X, Homma S, Drosatos K, Lomasney J, Engman DM, Miller SD, Vaughan DE, Morrow JP, Kishore R, Thorp EB. Enhanced efferocytosis of apoptotic cardiomyocytes through myeloid-epithelial-reproductive tyrosine kinase links acute inflammation resolution to cardiac repair after infarction. Circ Res. 2013;113: 1004–12.WanEYeapXYDehnSTerryRNovakMZhangSIwataSHanXHommaSDrosatosKLomasneyJEngmanDMMillerSDVaughanDEMorrowJPKishoreRThorpEBEnhanced efferocytosis of apoptotic cardiomyocytes through myeloid-epithelial-reproductive tyrosine kinase links acute inflammation resolution to cardiac repair after infarctionCirc Res.201311310041210.1161/CIRCRESAHA.113.301198384046423836795Search in Google Scholar
Hanna RN, Carlin LM, Hubbeling HG, Nackiewicz D, Green AM, Punt JA, Geissmann F, Hedrick CC. The transcription factor NR4A1 (Nur77) controls bone marrow differentiation and the survival of Ly6C- monocytes. Nat Immunol. 2011;12: 778–85.HannaRNCarlinLMHubbelingHGNackiewiczDGreenAMPuntJAGeissmannFHedrickCCThe transcription factor NR4A1 (Nur77) controls bone marrow differentiation and the survival of Ly6C- monocytesNat Immunol.2011127788510.1038/ni.2063332439521725321Search in Google Scholar
Seropian IM, Toldo S, Van Tassell BW, Abbate A. Anti-inflammatory strategies for ventricular remodeling following ST-segment elevation acute myocardial infarction. J Am Coll Cardiol. 2014;63: 1593–603.SeropianIMToldoSVan TassellBWAbbateAAnti-inflammatory strategies for ventricular remodeling following ST-segment elevation acute myocardial infarctionJ Am Coll Cardiol.201463159360310.1016/j.jacc.2014.01.01424530674Search in Google Scholar
Westman PC, Lipinski MJ, Luger D, Waksman R, Bonow RO, Wu E, Epstein S. Inflammation as a Driver of Adverse Left Ventricular Remodeling After Acute Myocardial Infarction. J Am Coll Cardiol 2016;67(17): 2050–60.WestmanPCLipinskiMJLugerDWaksmanRBonowROWuEEpsteinSInflammation as a Driver of Adverse Left Ventricular Remodeling After Acute Myocardial InfarctionJ Am Coll Cardiol2016671720506010.1016/j.jacc.2016.01.07327126533Search in Google Scholar
Lugrin J, Roumen Parapanov R, Krueger T, Liaudet L. Murine Myocardial Infarction Model using Permanent Ligation of Left Anterior Descending Coronary Artery. J Vis Exp 2019;150: 1–7.LugrinJRoumen ParapanovRKruegerTLiaudetLMurine Myocardial Infarction Model using Permanent Ligation of Left Anterior Descending Coronary ArteryJ Vis Exp20191501710.3791/5959131475987Search in Google Scholar
Aisyah S, Ghafar NA, Jubri Z, Das S. Induction of Myocardial Infarction in Experimental Animals: A Review. Journal of Clinical and Diagnostic Research 2018; 12(11): 1–05.AisyahSGhafarNAJubriZDasSInduction of Myocardial Infarction in Experimental Animals: A ReviewJournal of Clinical and Diagnostic Research20181211105Search in Google Scholar
Nahrendorf M, Swirski FK, Aikawa E, Stangenberg L, Wurdinger T, Figueiredo JL, Libby P, Weissleder R, Pittet MJ. The healing myocardium sequentially mobilizes two monocyte subsets with divergent and complementary functions. The Journal of experimental medicine 2007;204: 3037–3047.NahrendorfMSwirskiFKAikawaEStangenbergLWurdingerTFigueiredoJLLibbyPWeisslederRPittetMJThe healing myocardium sequentially mobilizes two monocyte subsets with divergent and complementary functionsThe Journal of experimental medicine20072043037304710.1084/jem.20070885211851718025128Search in Google Scholar
Mares RG, Marinkovic G, Cotoi OS, Schiopu A. Innate Immune Mechanisms in Myocardial Infarction - An Update. Revista Romana de Medicina de Laborator 2018;26(1): 9–20.MaresRGMarinkovicGCotoiOSSchiopuAInnate Immune Mechanisms in Myocardial Infarction - An UpdateRevista Romana de Medicina de Laborator201826192010.1515/rrlm-2017-0031Search in Google Scholar
Hilgendorf I, Gerhardt L, Tan TC, Winter C, Holderried TA, Chousterman BG, Iwamoto Y, Liao R, Zirlik A, Scherer-Crosbie M, Hedrick CC, Libby P, Nahrendorf M, Weissleder R, Swirski RK. Ly-6Chigh Monocytes Depend on Nr4a1 to Balance both Inflammatory and Reparative Phases in the Infarcted Myocardium. Circulation Research 2014;114(10): 1611–1622.HilgendorfIGerhardtLTanTCWinterCHolderriedTAChoustermanBGIwamotoYLiaoRZirlikAScherer-CrosbieMHedrickCCLibbyPNahrendorfMWeisslederRSwirskiRKLy-6Chigh Monocytes Depend on Nr4a1 to Balance both Inflammatory and Reparative Phases in the Infarcted MyocardiumCirculation Research2014114101611162210.1161/CIRCRESAHA.114.303204401734924625784Search in Google Scholar
Kratofil RM, Kubes P, Deniset JF. Monocyte Conversion During Inflammation and Injury. Arterioscler Thromb Vasc Biol 2017;37(1): 35–42.KratofilRMKubesPDenisetJFMonocyte Conversion During Inflammation and InjuryArterioscler Thromb Vasc Biol2017371354210.1161/ATVBAHA.116.30819827765768Search in Google Scholar
Swirski FK. Inflammation and repair in the ischaemic myocardium. Hamostaseologie 2015;35: 34–6.SwirskiFKInflammation and repair in the ischaemic myocardiumHamostaseologie20153534610.5482/HAMO-14-09-004525375277Search in Google Scholar
Prabhu SD, Frangogiannis NG. The Biological Basis for Cardiac Repair After Myocardial Infarction: From Inflammation to Fibrosis. Circ Res 2016;119(1): 91–112.PrabhuSDFrangogiannisNGThe Biological Basis for Cardiac Repair After Myocardial Infarction: From Inflammation to FibrosisCirc Res201611919111210.1161/CIRCRESAHA.116.303577492252827340270Search in Google Scholar
Swirski FK, Nahrendorf M, Etzrodt M, Wildgruber M, Cortez-Retamozo V, Panizzi P, Figueiredo JL, Kohler RH, Chudnovskiy A, Waterman P, Aikawa E, Mempel TR, Libby P, Weissleder R, Pittet MJ. Identification of splenic reservoir monocytes and their deployment to inflammatory sites. Science 2009;325: 612–6.SwirskiFKNahrendorfMEtzrodtMWildgruberMCortez-RetamozoVPanizziPFigueiredoJLKohlerRHChudnovskiyAWatermanPAikawaEMempelTRLibbyPWeisslederRPittetMJIdentification of splenic reservoir monocytes and their deployment to inflammatory sitesScience2009325612610.1126/science.1175202280311119644120Search in Google Scholar
Howangyin KY, Zlatanova I, Pinto C, Ngkelo A, Cochain C, Rouanet M, Vilar J, Lemitre M, Stockmann C, Fleischmann BK, Mallat Z, Silvestre JS. Myeloid-Epithelial-Reproductive Receptor Tyrosine Kinase and Milk Fat Globule Epidermal Growth Factor 8 Coordinately Improve Remodeling After Myocardial Infarction via Local Delivery of Vascular Endothelial Growth Factor. Circulation 2016;133: 826–39.HowangyinKYZlatanovaIPintoCNgkeloACochainCRouanetMVilarJLemitreMStockmannCFleischmannBKMallatZSilvestreJSMyeloid-Epithelial-Reproductive Receptor Tyrosine Kinase and Milk Fat Globule Epidermal Growth Factor 8 Coordinately Improve Remodeling After Myocardial Infarction via Local Delivery of Vascular Endothelial Growth FactorCirculation20161338263910.1161/CIRCULATIONAHA.115.020857476710926819373Search in Google Scholar
Wynn TA, Vannella KM. Macrophages in Tissue Repair, Regeneration, and Fibrosis. Immunity 2016;44: 450–62.WynnTAVannellaKMMacrophages in Tissue Repair, Regeneration, and FibrosisImmunity2016444506210.1016/j.immuni.2016.02.015479475426982353Search in Google Scholar
Frangogiannis NG. Emerging roles for macrophages in cardiac injury: cytoprotection, repair, and regeneration. J Clin Invest 2015;125: 2927–30.FrangogiannisNGEmerging roles for macrophages in cardiac injury: cytoprotection, repair, and regenerationJ Clin Invest201512529273010.1172/JCI83191456376726214519Search in Google Scholar