References
- Saraste A, Voipio-Pulkki LM, Parvinen M, Pulkki K. Apoptosis in the heart. N Engl J Med 1997;336:1025-6; discussion 6. https://doi.org/10.1056/NEJM199704033361415
- Kang PM, Izumo S. Apoptosis in heart: basic mechanisms and implications in cardiovascular diseases. Trends Mol Med 2003;9:177-82. https://doi.org/10.1016/S1471-4914(03)00025-X
- Kang PM, Izumo S. Apoptosis and heart failure: a critical review of the literature. Circ Res 2000;86:1107-13. https://doi.org/10.1161/01.RES.86.11.1107
- Gottlieb RA, Burleson KO, Kloner RA, Babior BM, Engler RL. Reperfusion injury induces apoptosis in rabbit cardiomyocytes. J Clin Invest 1994;94:1621-8. https://doi.org/10.1172/JCI117504
- Olivetti G, Abbi R, Quaini F, et al. Apoptosis in the failing human heart. N Engl J Med 1997;336:1131-41. https://doi.org/10.1056/NEJM199704173361603
- Olivetti G, Quaini F, Sala R, et al. Acute myocardial infarction in humans is associated with activation of programmed myocyte cell death in the surviving portion of the heart. J Mol Cell Cardiol 1996;28: 2005-16. https://doi.org/10.1006/jmcc.1996.0193
- Takemura G, Ohno M, Hayakawa Y, et al. Role of apoptosis in the disappearance of infiltrated and proliferated interstitial cells after myocardial infarction. Circ Res 1998;82:1130-8. https://doi.org/10.1161/01.RES.82.11.1130
- Nicholson DW, Thornberry NA. Caspases: killer proteases. Trends Biochem Sci 1997;22:299-306. https://doi.org/10.1016/S0968-0004(97)01085-2
- Pop C, Salvesen GS. Human caspases: activation, specificity, and regulation. J Biol Chem 2009;284:21777-81. https://doi.org/10.1074/jbc.R800084200
- Zheng TS, Hunot S, Kuida K, Flavell RA. Caspase knockouts: matters of life and death. Cell Death Differ 1999;6:1043-53. https://doi.org/10.1038/sj.cdd.4400593
- Liu X, Kim CN, Yang J, Jemmerson R, Wang X. Induction of apoptotic program in cell-free extracts: requirement for dATP and cytochrome c. Cell 1996;86:147-57. https://doi.org/10.1016/S0092-8674(00)80085-9
- Li P, Nijhawan D, Budihardjo I, et al. Cytochrome c and dATP-dependent formation of Apaf-1/caspase-9 complex initiates an apoptotic protease cascade. Cell 1997;91:479-89. https://doi.org/10.1016/S0092-8674(00)80434-1
- Zou H, Henzel WJ, Liu X, Lutschg A, Wang X. Apaf-1, a human protein homologous to C. elegans CED-4, participates in cytochrome cdependent activation of caspase-3. Cell 1997;90:405-13. https://doi.org/10.1016/S0092-8674(00)80501-2
- Nagata S. Apoptosis by death factor. Cell 1997;88:355-65. https://doi.org/10.1016/S0092-8674(00)81874-7
- Slee EA, Harte MT, Kluck RM, et al. Ordering the cytochrome c-initiated caspase cascade: hierarchical activation of caspases-2, -3, -6, -7, -8, and -10 in a caspase-9-dependent manner. J Cell Biol 1999;144: 281-92. https://doi.org/10.1083/jcb.144.2.281
- Kang PM, Haunstetter A, Aoki H, Usheva A, Izumo S. Morphological and molecular characterization of adult cardiomyocyte apoptosis during hypoxia and reoxygenation. Circ Res 2000;87:118-25. https://doi.org/10.1161/01.RES.87.2.118
- Yeh WC, Pompa JL, McCurrach ME, et al. FADD: essential for embryo development and signaling from some, but not all, inducers of apoptosis. Science 1998;279:1954-8. https://doi.org/10.1126/science.279.5358.1954
- Ishiyama S, Hiroe M, Nishikawa T, et al. The Fas/Fas ligand system is involved in the pathogenesis of autoimmune myocarditis in rats. J Immunol 1998;161:4695-701.
- Twu C, Liu NQ, Popik W, et al. Cardiomyocytes undergo apoptosis in human immunodeficiency virus cardiomyopathy through mitochondrion- and death receptor-controlled pathways. Proc Natl Acad Sci U S A 2002;99:14386-91. https://doi.org/10.1073/pnas.212327899
- Doyama K, Fujiwara H, Fukumoto M, et al. Tumour necrosis factor is expressed in cardiac tissues of patients with heart failure. Int J Cardiol 1996;54:217-25. https://doi.org/10.1016/0167-5273(96)02607-1
- Torre-Amione G, Kapadia S, Lee J, et al. Tumor necrosis factor-alpha and tumor necrosis factor receptors in the failing human heart. Circulation 1996;93:704-11. https://doi.org/10.1161/01.CIR.93.4.704
- Bryant D, Becker L, Richardson J, et al. Cardiac failure in transgenic mice with myocardial expression of tumor necrosis factor-alpha. Circulation 1998;97:1375-81. https://doi.org/10.1161/01.CIR.97.14.1375
- Kubota T, McTiernan CF, Frye CS, et al. Dilated cardiomyopathy in transgenic mice with cardiac-specific overexpression of tumor necrosis factor-alpha. Circ Res 1997;81:627-35. https://doi.org/10.1161/01.RES.81.4.627
- Lee P, Sata M, Lefer DJ, Factor SM, Walsh K, Kitsis RN. Fas pathway is a critical mediator of cardiac myocyte death and MI during ischemia- reperfusion in vivo. Am J Physiol Heart Circ Physiol 2003;284: H456-63. https://doi.org/10.1152/ajpheart.00777.2002
- Nelson DP, Setser E, Hall DG, et al. Proinflammatory consequences of transgenic fas ligand expression in the heart. J Clin Invest 2000; 105:1199-208. https://doi.org/10.1172/JCI8212
- Kurrelmeyer KM, Michael LH, Baumgarten G, et al. Endogenous tumor necrosis factor protects the adult cardiac myocyte against ischemic- induced apoptosis in a murine model of acute myocardial infarction. Proc Natl Acad Sci U S A 2000;97:5456-61. https://doi.org/10.1073/pnas.070036297
- Bao Q, Shi Y. Apoptosome: a platform for the activation of initiator caspases. Cell Death Differ 2007;14:56-65. https://doi.org/10.1038/sj.cdd.4402028
- Youle RJ, Strasser A. The BCL-2 protein family: opposing activities that mediate cell death. Nat Rev Mol Cell Biol 2008;9:47-59. https://doi.org/10.1038/nrm2308
- Adams JM, Cory S. The Bcl-2 protein family: arbiters of cell survival. Science 1998;281:1322-6. https://doi.org/10.1126/science.281.5381.1322
- Li H, Zhu H, Xu CJ, Yuan J. Cleavage of BID by caspase 8 mediates the mitochondrial damage in the Fas pathway of apoptosis. Cell 1998; 94:491-501. https://doi.org/10.1016/S0092-8674(00)81590-1
- Brocheriou V, Hagege AA, Oubenaissa A, et al. Cardiac functional improvement by a human Bcl-2 transgene in a mouse model of ischemia/ reperfusion injury. J Gene Med 2000;2:326-33. https://doi.org/10.1002/1521-2254(200009/10)2:5<326::AID-JGM133>3.0.CO;2-1
- Chen Z, Chua CC, Ho YS, Hamdy RC, Chua BH. Overexpression of Bcl-2 attenuates apoptosis and protects against myocardial I/R injury in transgenic mice. Am J Physiol Heart Circ Physiol 2001;280:H2313- 20. https://doi.org/10.1152/ajpheart.2001.280.5.H2313
- Hochhauser E, Cheporko Y, Yasovich N, et al. Bax deficiency reduces infarct size and improves long-term function after myocardial infarction. Cell Biochem Biophys 2007;47:11-20. https://doi.org/10.1385/CBB:47:1:11
- Salvesen GS, Dixit VM. Caspase activation: the induced-proximity model. Proc Natl Acad Sci U S A 1999;96:10964-7. https://doi.org/10.1073/pnas.96.20.10964
- Sun CK, Chang LT, Sheu JJ, et al. Losartan preserves integrity of cardiac gap junctions and PGC-1 alpha gene expression and prevents cellular apoptosis in remote area of left ventricular myocardium following acute myocardial infarction. Int Heart J 2007;48:533-46. https://doi.org/10.1536/ihj.48.533
- Ekhterae D, Lin Z, Lundberg MS, Crow MT, Brosius FC 3rd, Nunez G. ARC inhibits cytochrome c release from mitochondria and protects against hypoxia-induced apoptosis in heart-derived H9c2 cells. Circ Res 1999;85:e70-7. https://doi.org/10.1161/01.RES.85.12.e70
- Koseki T, Inohara N, Chen S, Nunez G. ARC, an inhibitor of apoptosis expressed in skeletal muscle and heart that interacts selectively with caspases. Proc Natl Acad Sci U S A 1998;95:5156-60. https://doi.org/10.1073/pnas.95.9.5156
- Pyo JO, Nah J, Kim HJ, et al. Protection of cardiomyocytes from ischemic/ hypoxic cell death via Drbp1 and pMe2GlyDH in cardio-specific ARC transgenic mice. J Biol Chem 2008;283:30707-14. https://doi.org/10.1074/jbc.M804209200
- Han Y, Chen YS, Liu Z, et al. Overexpression of HAX-1 protects cardiac myocytes from apoptosis through caspase-9 inhibition. Circ Res 2006;99:415-23. https://doi.org/10.1161/01.RES.0000237387.05259.a5
- Bae S, Yalamarti B, Kang PM. Role of caspase-independent apoptosis in cardiovascular diseases. Front Biosci 2008;13:2495-503. https://doi.org/10.2741/2861
- Lorenzo HK, Susin SA, Penninger J, Kroemer G. Apoptosis inducing factor (AIF): a phylogenetically old, caspase-independent effector of cell death. Cell Death Differ 1999;6:516-24. https://doi.org/10.1038/sj.cdd.4400527
- Penninger JM, Kroemer G. Mitochondria, AIF and caspases: rivaling for cell death execution. Nat Cell Biol 2003;5:97-9. https://doi.org/10.1038/ncb0203-97
- Cande C, Cecconi F, Dessen P, Kroemer G. Apoptosis-inducing factor (AIF): key to the conserved caspase-independent pathways of cell death? J Cell Sci 2002;115:4727-34. https://doi.org/10.1242/jcs.00210
- Cregan SP, Dawson VL, Slack RS. Role of AIF in caspase-dependent and caspase-independent cell death. Oncogene 2004;23:2785-96. https://doi.org/10.1038/sj.onc.1207517
- Cregan SP, Fortin A, MacLaurin JG, et al. Apoptosis-inducing factor is involved in the regulation of caspase-independent neuronal cell death. J Cell Biol 2002;158:507-17. https://doi.org/10.1083/jcb.200202130
- Susin SA, Lorenzo HK, Zamzami N, et al. Molecular characterization of mitochondrial apoptosis-inducing factor. Nature 1999;397:441-6. https://doi.org/10.1038/17135
- Vahsen N, Cande C, Briere JJ, et al. AIF deficiency compromises oxidative phosphorylation. EMBO J 2004;23:4679-89. https://doi.org/10.1038/sj.emboj.7600461
- Sharp TV, Wang HW, Koumi A, et al. K15 protein of Kaposi's sarcoma- associated herpesvirus is latently expressed and binds to HAX-1, a protein with antiapoptotic function. J Virol 2002;76:802-16. https://doi.org/10.1128/JVI.76.2.802-816.2002
- Chen M, Zsengeller Z, Xiao CY, Szabo C. Mitochondrial-to-nuclear translocation of apoptosis-inducing factor in cardiac myocytes during oxidant stress: potential role of poly (ADP-ribose) polymerase-1. Cardiovasc Res 2004;63:682-8. https://doi.org/10.1016/j.cardiores.2004.04.018
- Xiao CY, Chen M, Zsengeller Z, et al. Poly (ADP-Ribose) polymerase promotes cardiac remodeling, contractile failure, and translocation of apoptosis-inducing factor in a murine experimental model of aortic banding and heart failure. J Pharmacol Exp Ther 2005;312:891-8.
- Kim GT, Chun YS, Park JW, Kim MS. Role of apoptosis-inducing factor in myocardial cell death by ischemia-reperfusion. Biochem Biophys Res Commun 2003;309:619-24. https://doi.org/10.1016/j.bbrc.2003.08.045
- Siu PM, Bae S, Bodyak N, Rigor DL, Kang PM. Response of caspaseindependent apoptotic factors to high salt diet-induced heart failure. J Mol Cell Cardiol 2007;42:678-86. https://doi.org/10.1016/j.yjmcc.2007.01.001
- Choudhury S, Bae S, Kumar SR, et al. Role of AIF in cardiac apoptosis in hypertrophic cardiomyocytes from Dahl salt-sensitive rats. Cardiovasc Res 2010;85:28-37. https://doi.org/10.1093/cvr/cvp261
- Joza N, Susin SA, Daugas E, et al. Essential role of the mitochondrial apoptosis-inducing factor in programmed cell death. Nature 2001; 410:549-54. https://doi.org/10.1038/35069004
- van Empel VP, Bertrand AT, van der Nagel R, et al. Downregulation of apoptosis-inducing factor in harlequin mutant mice sensitizes the myocardium to oxidative stress-related cell death and pressure overload- induced decompensation. Circ Res 2005;96:e92-101. https://doi.org/10.1161/01.RES.0000172081.30327.28
- Joza N, Oudit GY, Brown D, et al. Muscle-specific loss of apoptosisinducing factor leads to mitochondrial dysfunction, skeletal muscle atrophy, and dilated cardiomyopathy. Mol Cell Biol 2005;25:10261-72. https://doi.org/10.1128/MCB.25.23.10261-10272.2005
- Cheung EC, Joza N, Steenaart NA, et al. Dissociating the dual roles of apoptosis-inducing factor in maintaining mitochondrial structure and apoptosis. EMBO J 2006;25:4061-73. https://doi.org/10.1038/sj.emboj.7601276
- David KK, Sasaki M, Yu SW, Dawson TM, Dawson VL. EndoG is dispensable in embryogenesis and apoptosis. Cell Death Differ 2006; 13:1147-55. https://doi.org/10.1038/sj.cdd.4401787
- Irvine RA, Adachi N, Shibata DK, et al. Generation and characterization of endonuclease G null mice. Mol Cell Biol 2005;25:294-302. https://doi.org/10.1128/MCB.25.1.294-302.2005
- Li LY, Luo X, Wang X. Endonuclease G is an apoptotic DNase when released from mitochondria. Nature 2001;412:95-9. https://doi.org/10.1038/35083620
- Bahi N, Zhang J, Llovera M, Ballester M, Comella JX, Sanchis D. Switch from caspase-dependent to caspase-independent death during heart development: essential role of endonuclease in ischemia-induced DNA processing on differentiated cardiomyocytes. J Biol Chem 2006; 281:22943-52. https://doi.org/10.1074/jbc.M601025200
- Suzuki Y, Takahashi-Niki K, Akagi T, Hashikawa T, Takahashi R. Mitochondrial protease Omi/HtrA2 enhances caspase activation through multiple pathways. Cell Death Differ 2004;11:208-16. https://doi.org/10.1038/sj.cdd.4401343
- Liu HR, Gao E, Hu A, et al. Role of Omi/HtrA2 in apoptotic cell death after myocardial ischemia and reperfusion. Circulation 2005;111:90-6. https://doi.org/10.1161/01.CIR.0000151613.90994.17
- Li Z, Zhang T, Dai H, et al. Involvement of endoplasmic reticulum stress in myocardial apoptosis of streptozocin-induced diabetic rats. J Clin Biochem Nutr 2007;41:58-67. https://doi.org/10.3164/jcbn.2007008
- Hamada H, Suzuki M, Yuasa S, et al. Dilated cardiomyopathy caused by aberrant endoplasmic reticulum quality control in mutant KDEL receptor transgenic mice. Mol Cell Biol 2004;24:8007-17. https://doi.org/10.1128/MCB.24.18.8007-8017.2004
- Szegezdi E, Logue SE, Gorman AM, Samali A. Mediators of endoplasmic reticulum stress-induced apoptosis. EMBO Rep 2006;7:880-5. https://doi.org/10.1038/sj.embor.7400779
- Li J, Lee B, Lee AS. Endoplasmic reticulum stress-induced apoptosis: multiple pathways and activation of p53-up-regulated modulator of apoptosis (PUMA) and NOXA by p53. J Biol Chem 2006;281:7260-70. https://doi.org/10.1074/jbc.M509868200
- Nickson P, Toth A, Erhardt P. PUMA is critical for neonatal cardiomyocyte apoptosis induced by endoplasmic reticulum stress. Cardiovasc Res 2007;73:48-56. https://doi.org/10.1016/j.cardiores.2006.10.001
- Scorrano L, Oakes SA, Opferman JT, et al. BAX and BAK regulation of endoplasmic reticulum Ca2+: a control point for apoptosis. Science 2003;300:135-9. https://doi.org/10.1126/science.1081208
- Degterev A, Huang Z, Boyce M, et al. Chemical inhibitor of nonapoptotic cell death with therapeutic potential for ischemic brain injury. Nat Chem Biol 2005;1:112-9. https://doi.org/10.1038/nchembio711
- Kim J, Klionsky DJ. Autophagy, cytoplasm-to-vacuole targeting pathway, and pexophagy in yeast and mammalian cells. Annu Rev Biochem 2000;69:303-42. https://doi.org/10.1146/annurev.biochem.69.1.303
- Gorski SM, Chittaranjan S, Pleasance ED, et al. A SAGE approach to discovery of genes involved in autophagic cell death. Curr Biol 2003; 13:358-63. https://doi.org/10.1016/S0960-9822(03)00082-4
- Lee CY, Baehrecke EH. Steroid regulation of autophagic programmed cell death during development. Development 2001;128:1443-55.
- Liang XH, Jackson S, Seaman M, et al. Induction of autophagy and inhibition of tumorigenesis by beclin 1. Nature 1999;402:672-6. https://doi.org/10.1038/45257
- Berry DL, Baehrecke EH. Growth arrest and autophagy are required for salivary gland cell degradation in Drosophila. Cell 2007;131: 1137-48. https://doi.org/10.1016/j.cell.2007.10.048
- Laugwitz KL, Moretti A, Weig HJ, et al. Blocking caspase-activated apoptosis improves contractility in failing myocardium. Hum Gene Ther 2001;12:2051-63. https://doi.org/10.1089/10430340152677403
- Yaoita H, Ogawa K, Maehara K, Maruyama Y. Attenuation of ischemia/ reperfusion injury in rats by a caspase inhibitor. Circulation 1998;97:276-81. https://doi.org/10.1161/01.CIR.97.3.276
- Okamura T, Miura T, Takemura G, et al. Effect of caspase inhibitors on myocardial infarct size and myocyte DNA fragmentation in the ischemia- reperfused rat heart. Cardiovasc Res 2000;45:642-50. https://doi.org/10.1016/S0008-6363(99)00271-0
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