Guidelines for the use and interpretation of assays for monitoring cell death in higher eukaryotes

被引:529
作者
Galluzzi, L. [1 ,2 ]
Aaronson, S. A. [3 ]
Abrams, J. [4 ]
Alnemri, E. S.
Andrews, D. W. [5 ,6 ]
Baehrecke, E. H. [7 ]
Bazan, N. G. [8 ]
Blagosklonny, M. V. [9 ]
Blomgren, K. [10 ,11 ]
Borner, C. [12 ]
Bredesen, D. E. [13 ,14 ]
Brenner, C. [15 ,16 ]
Castedo, M. [1 ,2 ]
Cidlowski, J. A. [17 ]
Ciechanover, A. [18 ]
Cohen, G. M. [19 ]
De Laurenzi, V. [20 ]
De Maria, R. [21 ,22 ]
Deshmukh, M. [23 ]
Dynlacht, B. D. [24 ]
El-Deiry, W. S. [25 ]
Flavell, R. A. [26 ,27 ]
Fulda, S. [28 ]
Garrido, C. [29 ,30 ]
Golstein, P. [31 ,32 ,33 ]
Gougeon, M-L [34 ]
Green, D. R. [35 ]
Gronemeyer, H. [36 ,37 ,38 ]
Hajnoczky, G. [39 ]
Hardwick, J. M. [40 ]
Hengartner, M. O. [41 ]
Ichijo, H. [42 ]
Jaattela, M. [43 ]
Kepp, O. [1 ,2 ]
Kimchi, A. [44 ]
Klionsky, D. J. [45 ,46 ]
Knight, R. A. [47 ]
Kornbluth, S. [48 ]
Kumar, S. [49 ]
Levine, B. [27 ,50 ]
Lipton, S. A. [51 ,52 ,53 ,54 ]
Lugli, E. [55 ]
Madeo, F. [56 ]
Malorni, W. [57 ]
Marine, J-C W. [58 ,59 ]
Martin, S. J. [60 ]
Medema, J. P. [61 ,62 ]
Mehlen, P. [63 ,64 ,65 ]
Melino, G. [19 ,66 ]
Moll, U. M. [67 ,68 ,69 ]
机构
[1] Inst Gustave Roussy, INSERM, U848, F-94805 Villejuif, France
[2] Univ Paris 11, F-94805 Villejuif, France
[3] Mt Sinai Sch Med, Dept Oncol Sci, New York, NY 10029 USA
[4] Univ Texas SW Med Ctr Dallas, Dept Cell Biol, Dallas, TX 75390 USA
[5] Thomas Jefferson Univ, Kimmel Canc Inst, Ctr Apoptosis Res, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA
[6] McMaster Univ, Dept Biochem & Biomed Sci, Hamilton, ON L8N 3Z5, Canada
[7] Univ Massachusetts, Sch Med, Dept Canc Biol, Worcester, MA 01605 USA
[8] Louisiana State Univ, Hlth Sci Ctr, Sch Med, Neurosci Ctr Excellence, New Orleans, LA 70112 USA
[9] Roswell Pk Canc Inst, Buffalo, NY 14263 USA
[10] Univ Gothenburg, Inst Neurosci & Physiol, Ctr Brain Repair & Rehabil, SE-40530 Gothenburg, Sweden
[11] Queen Silvia Childrens Hosp, Dept Pediat Oncol, SE-41685 Gothenburg, Sweden
[12] Univ Freiburg, Inst Mol Med & Cell Res ZBMZ, D-79104 Freiburg, Germany
[13] Buck Inst Age Res, Novato, CA 94945 USA
[14] Univ Calif San Francisco, San Francisco, CA 94143 USA
[15] Univ Versailles St Quentin, F-78035 Versailles, France
[16] CNRS, UMR8159, F-78035 Versailles, France
[17] Natl Inst Environm Hlth Sci, NIH, Duhram, NC 27709 USA
[18] Technion Israel Inst Technol, Rappaport Fac Med, Vasc & Tumor Biol Res Ctr, IL-31096 Haifa, Israel
[19] Univ Leicester, Toxicol Unit, MRC, Leicester LE1 9HN, Leics, England
[20] Univ G dAnnunzio, Dipartimento Sci Biomed, I-66100 Chieti, Italy
[21] Ist Super Sanita, Dept Hematol Oncol & Mol Med, I-00161 Rome, Italy
[22] Mediterranean Inst Oncol, I-95030 Catania, Italy
[23] Univ N Carolina, Dept Cell & Dev Biol, Ctr Neurosci, Chapel Hill, NC 27599 USA
[24] NYU, Sch Med, Dept Pathol, New York, NY 10016 USA
[25] Univ Penn, Sch Med, Div Hematol Oncol, Philadelphia, PA 19104 USA
[26] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
[27] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA
[28] Univ Childrens Hosp, D-89075 Ulm, Germany
[29] INSERM, UMR866, F-21049 Dijon, France
[30] Univ Burgundy, Fac Med & Pharm, F-21049 Dijon, France
[31] INSERM, U631, F-13288 Marseille, France
[32] CNRS, UMR6102, F-13288 Marseille, France
[33] Aix Marseille Univ, Ctr Immunol Marseille Luminy, F-13288 Marseille, France
[34] Inst Pasteur, Antiviral Immun Biotherapy & Vaccine Unit, F-75015 Paris, France
[35] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
[36] Inst Genet & Biol Mol & Cellulaire, Dept Canc Biol, F-67404 Illkirch Graffenstaden, France
[37] CNRS, UMR7104, F-67404 Illkirch Graffenstaden, France
[38] INSERM, U964, F-67404 Illkirch Graffenstaden, France
[39] Thomas Jefferson Univ, Dept Pathol Anat & Cell Biol, Philadelphia, PA 19107 USA
[40] Johns Hopkins Univ, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
[41] Univ Zurich, Inst Mol Biol, CH-8057 Zurich, Switzerland
[42] Univ Tokyo, Grad Sch Pharmaceut Sci, Tokyo 1130033, Japan
[43] Inst Canc Biol, Dept Apoptosis, Danish Canc Soc, DK-2100 Copenhagen, Denmark
[44] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
[45] Univ Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
[46] Univ Michigan, Dept Mol Cellular & Dev Biol & Biol Chem, Ann Arbor, MI 48109 USA
[47] UCL, Inst Child Hlth, London WC1N 1EH, England
[48] Duke Univ, Sch Med, Durham, NC 27710 USA
[49] Ctr Canc Biol, Hanson Inst, Adelaide, SA 5000, Australia
[50] Univ Texas SW Med Ctr Dallas, Dallas, TX 75390 USA
基金
英国惠康基金; 英国医学研究理事会;
关键词
apoptosis; caspases; cytofluorometry; immunofluorescence microscopy; mitotic catastrophe; necrosis; MITOCHONDRIAL-MEMBRANE PERMEABILIZATION; INDUCED THYMOCYTE APOPTOSIS; CYTOCHROME-C; CANCER-CELLS; OXIDATIVE STRESS; FLOW-CYTOMETRY; NUCLEAR-DNA; AUTOPHAGY; DROSOPHILA; RELEASE;
D O I
10.1038/cdd.2009.44
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cell death is essential for a plethora of physiological processes, and its deregulation characterizes numerous human diseases. Thus, the in-depth investigation of cell death and its mechanisms constitutes a formidable challenge for fundamental and applied biomedical research, and has tremendous implications for the development of novel therapeutic strategies. It is, therefore, of utmost importance to standardize the experimental procedures that identify dying and dead cells in cell cultures and/or in tissues, from model organisms and/or humans, in healthy and/or pathological scenarios. Thus far, dozens of methods have been proposed to quantify cell death-related parameters. However, no guidelines exist regarding their use and interpretation, and nobody has thoroughly annotated the experimental settings for which each of these techniques is most appropriate. Here, we provide a nonexhaustive comparison of methods to detect cell death with apoptotic or nonapoptotic morphologies, their advantages and pitfalls. These guidelines are intended for investigators who study cell death, as well as for reviewers who need to constructively critique scientific reports that deal with cellular demise. Given the difficulties in determining the exact number of cells that have passed the point-of-no-return of the signaling cascades leading to cell death, we emphasize the importance of performing multiple, methodologically unrelated assays to quantify dying and dead cells. Cell Death and Differentiation (2009) 16, 1093-1107; doi:10.1038/cdd.2009.44; published online 17 April 2009
引用
收藏
页码:1093 / 1107
页数:15
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