Physiological Consequences of Programmed Necrosis, an Alternative form of Cell Demise

Molecules and Cells

Volumn 29, Issue 4, 2010, Pages 327-332

  Cho, Young Sik ^b   Park, Seung Yeon ^b   Shin, Hee Suk ^b   Chan, Francis Ka Ming ^a  

^a UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL   (United States)

^b Korea Research Institute of Chemical Technology   (South Korea)

Author keywords

apoptosis; inflammation; programmed necrosis; receptor interacting protein; TNF

Indexed keywords

CASPASE; TUMOR NECROSIS FACTOR; CASPASE 8; DEATH RECEPTOR; NICOTINAMIDE ADENINE DINUCLEOTIDE ADENOSINE DIPHOSPHATE RIBOSYLTRANSFERASE;

APOPTOSIS; CELL DEATH; DRUG THERAPY; HUMAN; INFLAMMATION; INNATE IMMUNITY; NECROSIS; NONHUMAN; PHARMACOLOGY; REVIEW; SIGNAL TRANSDUCTION; ANIMAL; BIOLOGICAL MODEL; CELL SURVIVAL; IMMUNOLOGY; METABOLISM; PATHOPHYSIOLOGY; PHYSIOLOGY; VIRUS INFECTION;

ANIMALS; APOPTOSIS; CASPASE 8; CELL SURVIVAL; HUMANS; MODELS, BIOLOGICAL; NECROSIS; POLY(ADP-RIBOSE) POLYMERASES; RECEPTORS, DEATH DOMAIN; VIRUS DISEASES;

EID: 77956051110     PISSN: 10168478     EISSN: 02191032     Source Type: Journal    
DOI: 10.1007/s10059-010-0066-3     Document Type: Review

References (34)

1. Adams, S., Pankow, S., Werner, S., Munz, B., Regulation of NF-kappaB activity and keratinocyte differentiation by the RIP4 protein: implications for cutaneous wound repair. J. Invest. Dermatol. 127 (2007), 538–544.
2. Agostinis, P., Buytaert, E., Breyssens, H., Hendrickx, N., Regulatory pathways in photodynamic therapy induced apoptosis. Photochem. Photobiol. Sci. 3 (2004), 721–729.
3. Cauwels, A., Janssen, B., Waeytens, A., Cuvelier, C., Brouc-kaert, P., Caspase inhibition causes hyperacute tumor necrosis factor-induced shock via oxidative stress and phospholipase A2. Nat. Immunol. 4 (2003), 387–393.
4. Chan, F.K., Shisler, J., Bixby, J.G., Felices, M., Zheng, L., Appel, M., Orenstein, J., Moss, B., Lenardo, M.J., A role for tumor necrosis factor receptor-2 and receptor-interacting protein in programmed necrosis and antiviral responses. J. Biol. Chem. 278 (2003), 51613–51621.
5. Cho, Y.S., Challa, S., Moquin, D., Genga, R., Ray, T.D., Guildford, M., Chan, F.K., Phosphorylation-driven assembly of the RIP1-RIP3 complex regulates programmed necrosis and virus-induced inflammation. Cell 137 (2009), 1112–1123.
6. Cinquepalmi, L., Boni, L., Dionigi, G., Rovera, F., Diurni, M., Benevento, A., Dionigi, R., Long-term results and quality of life of patients undergoing sequential surgical treatment for severe acute pancreatitis complicated by infected pancreatic necrosis. Surg. Infect. 7 (2006), S113–116.
7. de Murcia, G., Schreiber, V., Molinete, M., Saulier, B., Poch, O., Masson, M., Niedergang, C., Menissier de Murcia, J., Structure and function of poly(ADP-ribose) polymerase. Mol. Cell. Biochem. 138 (1994), 15–24.
8. Degterev, A., Hitomi, J., Germscheid, M., Ch'en, I.L., Korkina, O., Teng, X., Abbott, D., Cuny, G.D., Yuan, C., Wagner, G., et al. Identification of RIP1 kinase as a specific cellular target of necrostatins. Nat. Chem. Biol. 4 (2008), 313–321.
9. Eigenbrod, T., Park, J.H., Harder, J., Iwakura, Y., Nunez, G., Cutting edge: critical role for mesothelial cells in necrosis-induced inflammation through the recognition of IL-1 alpha released from dying cells. J. Immunol. 181 (2008), 8194–8198.
10. Galluzzi, L., Kroemer, G., Necroptosis: a specialized pathway of programmed necrosis. Cell 135 (2008), 1161–1163.
11. Galluzzi, L., Kroemer, G., Shigella targets the mitochondrial checkpoint of programmed necrosis. Cell Host Microbe 5 (2009), 107–109.
12. Han, W., Xie, J., Li, L., Liu, Z., Hu, X., Necrostatin-1 reverts shikonin-induced necroptosis to apoptosis. Apoptosis 14 (2009), 674–686.
13. Hartwig, A., Asmuss, M., Blessing, H., Hoffmann, S., Jahnke, G., Khandelwal, S., Pelzer, A., Burkle, A., Interference by toxic metal ions with zinc-dependent proteins involved in maintaining genomic stability. Food Chem. Toxicol. 40 (2002), 1179–1184.
14. He, S., Wang, L., Miao, L., Wang, T., Du, F., Zhao, L., Wang, X., Receptor interacting protein kinase-3 determines cellular necrotic response to TNF-alpha. Cell 137 (2009), 1100–1111.
15. Hitomi, J., Christofferson, D.E., Ng, A., Yao, J., Degterev, A., Xavier, R.J., Yuan, J., Identification of a molecular signaling network that regulates a cellular necrotic cell death pathway. Cell 135 (2008), 1311–1323.
16. Holler, N., Zaru, R., Micheau, O., Thome, M., Attinger, A., Valitutti, S., Bodmer, J.L., Schneider, P., Seed, B., Tschopp, J., Fas triggers an alternative, caspase-8-independent cell death pathway using the kinase RIP as effector molecule. Nat. Immunol. 1 (2000), 489–495.
17. Hsu, T.S., Yang, P.M., Tsai, J.S., Lin, L.Y., Attenuation of cadmium-induced necrotic cell death by necrostatin-1: potential necrostatin-1 acting sites. Toxicol. Appl. Pharmacol. 235 (2009), 153–162.
18. Joza, N., Susin, S.A., Daugas, E., Stanford, W.L., Cho, S.K., Li, C.Y., Sasaki, T., Elia, A.J., Cheng, H.Y., Ravagnan, L., et al. Essential role of the mitochondrial apoptosis-inducing factor in programmed cell death. Nature 410 (2001), 549–554.
19. Kang, Y.H., Yi, M.J., Kim, M.J., Park, M.T., Bae, S., Kang, C.M., Cho, C.K., Park, I.C., Park, M.J., Rhee, C.H., et al. Caspase-independent cell death by arsenic trioxide in human cervical cancer cells: reactive oxygen species-mediated poly(ADP-ribose) polymerase-1 activation signals apoptosis-inducing factor release from mitochondria. Cancer Res. 64 (2004), 8960–8967.
20. Krysko, D.V., D'Herde, K., Vandenabeele, P., Clearance of apoptotic and necrotic cells and its immunological consequences. Apoptosis 11 (2006), 1709–1726.
21. Lautier, D., Lagueux, J., Thibodeau, J., Menard, L., Poirier, G.G., Molecular and biochemical features of poly (ADP-ribose) metabolism. Mol. Cell. Biochem. 122 (1993), 171–193.
22. Lin, Y., Choksi, S., Shen, H.M., Yang, Q.F., Hur, G.M., Kim, Y.S., Tran, J.H., Nedospasov, S.A., Liu, Z.G., Tumor necrosis factor-induced nonapoptotic cell death requires receptorinteracting protein-mediated cellular reactive oxygen species accumulation. J. Biol. Chem. 279 (2004), 10822–10828.
23. Micheau, O., Tschopp, J., Induction of TNF receptor I-mediated apoptosis via two sequential signaling complexes. Cell 114 (2003), 181–190.
24. Moubarak, R.S., Yuste, V.J., Artus, C., Bouharrour, A., Greer, P.A., Menissier-de Murcia, J., Susin, S.A., Sequential activation of poly(ADP-ribose) polymerase 1, calpains, and Bax is essential in apoptosis-inducing factor-mediated programmed necrosis. Mol. Cell. Biol. 27 (2007), 4844–4862.
25. Nakagawa, T., Shimizu, S., Watanabe, T., Yamaguchi, O., Otsu, K., Yamagata, H., Inohara, H., Kubo, T., Tsujimoto, Y., Cyclophilin D-dependent mitochondrial permeability transition regulates some necrotic but not apoptotic cell death. Nature 434 (2005), 652–658.
26. Pardo, J., Galvez, E.M., Koskinen, A., Simon, M.M., Lobigs, M., Regner, M., Mullbacher, A., Caspase-dependent inhibition of mousepox replication by gzmB. PloS one, 4, 2009, e7512.
27. Petit, F., Arnoult, D., Viollet, L., Estaquier, J., Intrinsic and extrinsic pathways signaling during HIV-1 mediated cell death. Biochimie 85 (2003), 795–811.
28. Porcelli, S.A., Jacobs, W.R.Jr., Tuberculosis: unsealing the apoptotic envelope. Nat. Immunol. 9 (2008), 1101–1102.
29. Riedl, S.J., Salvesen, G.S., The apoptosome: signalling platform of cell death. Nat. Rev. 8 (2007), 405–413.
30. Strasser, A., O'Connor, L., Dixit, V.M., Apoptosis signaling. Ann. Rev. Biochem. 69 (2000), 217–245.
31. Xu, Y., Huang, S., Liu, Z.G., Han, J., Poly(ADP-ribose) polymerase-1 signaling to mitochondria in necrotic cell death requires RIP1/TRAF2-mediated JNK1 activation. J. Biol. Chem. 281 (2006), 8788–8795.
32. Yang, P.M., Chen, H.C., Tsai, J.S., Lin, L.Y., Cadmium induces Ca2+-dependent necrotic cell death through calpaintriggered mitochondrial depolarization and reactive oxygen species-mediated inhibition of nuclear factor-kappaB activity. Chem. Res. Toxicol. 20 (2007), 406–415.
33. Zhang, D.W., Shao, J., Lin, J., Zhang, N., Lu, B.J., Lin, S.C., Dong, M.Q., Han, J., RIP3, an energy metabolism regulator that switches TNF-induced cell death from apoptosis to necrosis. Science 325 (2009), 332–336.
34. Zong, W.X., Ditsworth, D., Bauer, D.E., Wang, Z.Q., Thompson, C.B., Alkylating DNA damage stimulates a regulated form of necrotic cell death. Genes Dev. 18 (2004), 1272–1282.