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. 1993 Dec 1;123(5):1207–1222. doi: 10.1083/jcb.123.5.1207

Temporal analysis of events associated with programmed cell death (apoptosis) of sympathetic neurons deprived of nerve growth factor

PMCID: PMC2119882  PMID: 7503996

Abstract

The time course of molecular events that accompany degeneration and death after nerve growth factor (NGF) deprivation and neuroprotection by NGF and other agents was examined in cultures of NGF-dependent neonatal rat sympathetic neurons and compared to death by apoptosis. Within 12 h after onset of NGF deprivation, glucose uptake, protein synthesis, and RNA synthesis fell precipitously followed by a moderate decrease of mitochondrial function. The molecular mechanisms underlying the NGF deprivation-induced decrease of protein synthesis and neuronal death were compared and found to be different, demonstrating that this decrease of protein synthesis is insufficient to cause death subsequently. After these early changes and during the onset of neuronal atrophy, inhibition of protein synthesis ceased to halt neuronal degeneration while readdition of NGF or a cAMP analogue remained neuroprotective for 6 h. This suggests a model in which a putative killer protein reaches lethal levels several hours before the neurons cease to respond to readdition of NGF with survival and become committed to die. Preceding loss of viability by 5 h and concurrent with commitment to die, the neuronal DNA fragmented into oligonucleosomes. The temporal and pharmacological characteristics of DNA fragmentation is consistent with DNA fragmentation being part of the mechanism that commits the neuron to die. The antimitotic and neurotoxin cytosine arabinoside induced DNA fragmentation in the presence of NGF, supporting previous evidence that it mimicked NGF deprivation-induced death closely. Thus trophic factor deprivation- induced death occurs by apoptosis and is an example of programmed cell death.

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Selected References

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  1. Arends M. J., Morris R. G., Wyllie A. H. Apoptosis. The role of the endonuclease. Am J Pathol. 1990 Mar;136(3):593–608. [PMC free article] [PubMed] [Google Scholar]
  2. Arends M. J., Wyllie A. H. Apoptosis: mechanisms and roles in pathology. Int Rev Exp Pathol. 1991;32:223–254. doi: 10.1016/b978-0-12-364932-4.50010-1. [DOI] [PubMed] [Google Scholar]
  3. Barde Y. A. Trophic factors and neuronal survival. Neuron. 1989 Jun;2(6):1525–1534. doi: 10.1016/0896-6273(89)90040-8. [DOI] [PubMed] [Google Scholar]
  4. Batistatou A., Greene L. A. Aurintricarboxylic acid rescues PC12 cells and sympathetic neurons from cell death caused by nerve growth factor deprivation: correlation with suppression of endonuclease activity. J Cell Biol. 1991 Oct;115(2):461–471. doi: 10.1083/jcb.115.2.461. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Beaulaton J., Lockshin R. A. The relation of programmed cell death to development and reproduction: comparative studies and an attempt at classification. Int Rev Cytol. 1982;79:215–235. doi: 10.1016/s0074-7696(08)61675-7. [DOI] [PubMed] [Google Scholar]
  6. Bina-Stein M., Tritton T. R. Aurintricarboxylic acid is a nonspecific enzyme inhibitor. Mol Pharmacol. 1976 Jan;12(1):191–193. [PubMed] [Google Scholar]
  7. Bocchini V., Angeletti P. U. The nerve growth factor: purification as a 30,000-molecular-weight protein. Proc Natl Acad Sci U S A. 1969 Oct;64(2):787–794. doi: 10.1073/pnas.64.2.787. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Carmichael J., DeGraff W. G., Gazdar A. F., Minna J. D., Mitchell J. B. Evaluation of a tetrazolium-based semiautomated colorimetric assay: assessment of chemosensitivity testing. Cancer Res. 1987 Feb 15;47(4):936–942. [PubMed] [Google Scholar]
  9. Chang J. Y., Martin D. P., Johnson E. M., Jr Interferon suppresses sympathetic neuronal cell death caused by nerve growth factor deprivation. J Neurochem. 1990 Aug;55(2):436–445. doi: 10.1111/j.1471-4159.1990.tb04155.x. [DOI] [PubMed] [Google Scholar]
  10. Clarke P. G. Developmental cell death: morphological diversity and multiple mechanisms. Anat Embryol (Berl) 1990;181(3):195–213. doi: 10.1007/BF00174615. [DOI] [PubMed] [Google Scholar]
  11. Didier M., Heaulme M., Soubrié P., Bockaert J., Pin J. P. Rapid, sensitive, and simple method for quantification of both neurotoxic and neurotrophic effects of NMDA on cultured cerebellar granule cells. J Neurosci Res. 1990 Sep;27(1):25–35. doi: 10.1002/jnr.490270105. [DOI] [PubMed] [Google Scholar]
  12. Edwards S. N., Buckmaster A. E., Tolkovsky A. M. The death programme in cultured sympathetic neurones can be suppressed at the posttranslational level by nerve growth factor, cyclic AMP, and depolarization. J Neurochem. 1991 Dec;57(6):2140–2143. doi: 10.1111/j.1471-4159.1991.tb06434.x. [DOI] [PubMed] [Google Scholar]
  13. Erecińska M., Silver I. A. ATP and brain function. J Cereb Blood Flow Metab. 1989 Feb;9(1):2–19. doi: 10.1038/jcbfm.1989.2. [DOI] [PubMed] [Google Scholar]
  14. Fenton E. L. Tissue culture assay of nerve growth factor and of the specific antiserum. Exp Cell Res. 1970 Mar;59(3):383–392. doi: 10.1016/0014-4827(70)90645-2. [DOI] [PubMed] [Google Scholar]
  15. Ferrari G., Batistatou A., Greene L. A. Gangliosides rescue neuronal cells from death after trophic factor deprivation. J Neurosci. 1993 May;13(5):1879–1887. doi: 10.1523/JNEUROSCI.13-05-01879.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Frederickson R. M., Mushynski W. E., Sonenberg N. Phosphorylation of translation initiation factor eIF-4E is induced in a ras-dependent manner during nerve growth factor-mediated PC12 cell differentiation. Mol Cell Biol. 1992 Mar;12(3):1239–1247. doi: 10.1128/mcb.12.3.1239. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. González R. G., Blackburn B. J., Schleich T. Fractionation and structural elucidation of the active components of aurintricarboxylic acid, a potent inhibitor of protein nucleic acid interactions. Biochim Biophys Acta. 1979 May 24;562(3):534–545. doi: 10.1016/0005-2787(79)90116-3. [DOI] [PubMed] [Google Scholar]
  18. Gorin P. D., Johnson E. M. Experimental autoimmune model of nerve growth factor deprivation: effects on developing peripheral sympathetic and sensory neurons. Proc Natl Acad Sci U S A. 1979 Oct;76(10):5382–5386. doi: 10.1073/pnas.76.10.5382. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Gorin P. D., Johnson E. M., Jr Effects of long-term nerve growth factor deprivation on the nervous system of the adult rat: an experimental autoimmune approach. Brain Res. 1980 Sep 29;198(1):27–42. doi: 10.1016/0006-8993(80)90341-8. [DOI] [PubMed] [Google Scholar]
  20. Gunji H., Kharbanda S., Kufe D. Induction of internucleosomal DNA fragmentation in human myeloid leukemia cells by 1-beta-D-arabinofuranosylcytosine. Cancer Res. 1991 Jan 15;51(2):741–743. [PubMed] [Google Scholar]
  21. HESS H. H., POPE A. Ultramicrospectrophotometric determination of cytochrome oxidase for quantitative histochemistry. J Biol Chem. 1953 Sep;204(1):295–306. [PubMed] [Google Scholar]
  22. Halegoua S., Patrick J. Nerve growth factor mediates phosphorylation of specific proteins. Cell. 1980 Nov;22(2 Pt 2):571–581. doi: 10.1016/0092-8674(80)90367-0. [DOI] [PubMed] [Google Scholar]
  23. Hevner R. F., Wong-Riley M. T. Brain cytochrome oxidase: purification, antibody production, and immunohistochemical/histochemical correlations in the CNS. J Neurosci. 1989 Nov;9(11):3884–3898. doi: 10.1523/JNEUROSCI.09-11-03884.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Hevner R. F., Wong-Riley M. T. Regulation of cytochrome oxidase protein levels by functional activity in the macaque monkey visual system. J Neurosci. 1990 Apr;10(4):1331–1340. doi: 10.1523/JNEUROSCI.10-04-01331.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Huet O., Petit J. M., Ratinaud M. H., Julien R. NADH-dependent dehydrogenase activity estimation by flow cytometric analysis of 3-(4,5-dimethylthiazolyl-2-yl)-2,5-diphenyltetrazolium bromide (MTT) reduction. Cytometry. 1992;13(5):532–539. doi: 10.1002/cyto.990130513. [DOI] [PubMed] [Google Scholar]
  26. Jabbar S. A., Twentyman P. R., Watson J. V. The MTT assay underestimates the growth inhibitory effects of interferons. Br J Cancer. 1989 Oct;60(4):523–528. doi: 10.1038/bjc.1989.306. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Janjic D., Wollheim C. B. Islet cell metabolism is reflected by the MTT (tetrazolium) colorimetric assay. Diabetologia. 1992 May;35(5):482–485. doi: 10.1007/BF02342448. [DOI] [PubMed] [Google Scholar]
  28. Johnson E. M., Jr, Chang J. Y., Koike T., Martin D. P. Why do neurons die when deprived of trophic factor? Neurobiol Aging. 1989 Sep-Oct;10(5):549–553. doi: 10.1016/0197-4580(89)90127-9. [DOI] [PubMed] [Google Scholar]
  29. Johnson E. M., Jr, Deckwerth T. L. Molecular mechanisms of developmental neuronal death. Annu Rev Neurosci. 1993;16:31–46. doi: 10.1146/annurev.ne.16.030193.000335. [DOI] [PubMed] [Google Scholar]
  30. Johnson G. D., Nogueira Araujo G. M. A simple method of reducing the fading of immunofluorescence during microscopy. J Immunol Methods. 1981;43(3):349–350. doi: 10.1016/0022-1759(81)90183-6. [DOI] [PubMed] [Google Scholar]
  31. Johnson L. V., Walsh M. L., Bockus B. J., Chen L. B. Monitoring of relative mitochondrial membrane potential in living cells by fluorescence microscopy. J Cell Biol. 1981 Mar;88(3):526–535. doi: 10.1083/jcb.88.3.526. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Johnson M. I., Argiro V. Techniques in the tissue culture of rat sympathetic neurons. Methods Enzymol. 1983;103:334–347. doi: 10.1016/s0076-6879(83)03022-0. [DOI] [PubMed] [Google Scholar]
  33. Kauppinen R. A., Nicholls D. G. Synaptosomal bioenergetics. The role of glycolysis, pyruvate oxidation and responses to hypoglycaemia. Eur J Biochem. 1986 Jul 1;158(1):159–165. doi: 10.1111/j.1432-1033.1986.tb09733.x. [DOI] [PubMed] [Google Scholar]
  34. Kerr J. F., Wyllie A. H., Currie A. R. Apoptosis: a basic biological phenomenon with wide-ranging implications in tissue kinetics. Br J Cancer. 1972 Aug;26(4):239–257. doi: 10.1038/bjc.1972.33. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Koike T., Martin D. P., Johnson E. M., Jr Role of Ca2+ channels in the ability of membrane depolarization to prevent neuronal death induced by trophic-factor deprivation: evidence that levels of internal Ca2+ determine nerve growth factor dependence of sympathetic ganglion cells. Proc Natl Acad Sci U S A. 1989 Aug;86(16):6421–6425. doi: 10.1073/pnas.86.16.6421. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Koike T., Tanaka S. Evidence that nerve growth factor dependence of sympathetic neurons for survival in vitro may be determined by levels of cytoplasmic free Ca2+. Proc Natl Acad Sci U S A. 1991 May 1;88(9):3892–3896. doi: 10.1073/pnas.88.9.3892. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Koizumi S., Ryazanov A., Hama T., Chen H. C., Guroff G. Identification of Nsp100 as elongation factor 2 (EF-2). FEBS Lett. 1989 Aug 14;253(1-2):55–58. doi: 10.1016/0014-5793(89)80928-7. [DOI] [PubMed] [Google Scholar]
  38. Levi-Montalcini R., Booker B. DESTRUCTION OF THE SYMPATHETIC GANGLIA IN MAMMALS BY AN ANTISERUM TO A NERVE-GROWTH PROTEIN. Proc Natl Acad Sci U S A. 1960 Mar;46(3):384–391. doi: 10.1073/pnas.46.3.384. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Levi-Montalcini R., Caramia F., Angeletti P. U. Alterations in the fine structure of nucleoli in sympathetic neurons following NGF-antiserum treatment. Brain Res. 1969 Jan;12(1):54–73. doi: 10.1016/0006-8993(69)90055-9. [DOI] [PubMed] [Google Scholar]
  40. Lindhout E., Mevissen M. L., Kwekkeboom J., Tager J. M., de Groot C. Direct evidence that human follicular dendritic cells (FDC) rescue germinal centre B cells from death by apoptosis. Clin Exp Immunol. 1993 Feb;91(2):330–336. doi: 10.1111/j.1365-2249.1993.tb05904.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Makman M. H., Dvorkin B., White A. Alterations in protein and nucleic acid metabolism of thymocytes produced by adrenal steroids in vitro. J Biol Chem. 1966 Apr 10;241(7):1646–1648. [PubMed] [Google Scholar]
  42. Martin D. P., Ito A., Horigome K., Lampe P. A., Johnson E. M., Jr Biochemical characterization of programmed cell death in NGF-deprived sympathetic neurons. J Neurobiol. 1992 Nov;23(9):1205–1220. doi: 10.1002/neu.480230911. [DOI] [PubMed] [Google Scholar]
  43. Martin D. P., Schmidt R. E., DiStefano P. S., Lowry O. H., Carter J. G., Johnson E. M., Jr Inhibitors of protein synthesis and RNA synthesis prevent neuronal death caused by nerve growth factor deprivation. J Cell Biol. 1988 Mar;106(3):829–844. doi: 10.1083/jcb.106.3.829. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Martin D. P., Wallace T. L., Johnson E. M., Jr Cytosine arabinoside kills postmitotic neurons in a fashion resembling trophic factor deprivation: evidence that a deoxycytidine-dependent process may be required for nerve growth factor signal transduction. J Neurosci. 1990 Jan;10(1):184–193. doi: 10.1523/JNEUROSCI.10-01-00184.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. McConkey D. J., Hartzell P., Duddy S. K., Håkansson H., Orrenius S. 2,3,7,8-Tetrachlorodibenzo-p-dioxin kills immature thymocytes by Ca2+-mediated endonuclease activation. Science. 1988 Oct 14;242(4876):256–259. doi: 10.1126/science.3262923. [DOI] [PubMed] [Google Scholar]
  46. McConkey D. J., Hartzell P., Nicotera P., Orrenius S. Calcium-activated DNA fragmentation kills immature thymocytes. FASEB J. 1989 May;3(7):1843–1849. doi: 10.1096/fasebj.3.7.2497041. [DOI] [PubMed] [Google Scholar]
  47. Mendelsohn S. L., Nordeen S. K., Young D. A. Rapid changes in initiation-limited rates of protein synthesis in rat thymic lymphocytes correlate with energy charge. Biochem Biophys Res Commun. 1977 Nov 7;79(1):53–60. doi: 10.1016/0006-291x(77)90059-6. [DOI] [PubMed] [Google Scholar]
  48. Mesner P. W., Winters T. R., Green S. H. Nerve growth factor withdrawal-induced cell death in neuronal PC12 cells resembles that in sympathetic neurons. J Cell Biol. 1992 Dec;119(6):1669–1680. doi: 10.1083/jcb.119.6.1669. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 1983 Dec 16;65(1-2):55–63. doi: 10.1016/0022-1759(83)90303-4. [DOI] [PubMed] [Google Scholar]
  50. Munck A. Metabolic site and time course of cortisol action on glucose uptake, lactic acid output, and glucose 6-phosphate levels of rat thymus cells in vitro. J Biol Chem. 1968 Mar 10;243(5):1039–1042. [PubMed] [Google Scholar]
  51. Oppenheim R. W. Cell death during development of the nervous system. Annu Rev Neurosci. 1991;14:453–501. doi: 10.1146/annurev.ne.14.030191.002321. [DOI] [PubMed] [Google Scholar]
  52. Oppenheim R. W., Prevette D., Tytell M., Homma S. Naturally occurring and induced neuronal death in the chick embryo in vivo requires protein and RNA synthesis: evidence for the role of cell death genes. Dev Biol. 1990 Mar;138(1):104–113. doi: 10.1016/0012-1606(90)90180-q. [DOI] [PubMed] [Google Scholar]
  53. Otto D., Unsicker K., Grothe C. Pharmacological effects of nerve growth factor and fibroblast growth factor applied to the transectioned sciatic nerve on neuron death in adult rat dorsal root ganglia. Neurosci Lett. 1987 Dec 16;83(1-2):156–160. doi: 10.1016/0304-3940(87)90233-3. [DOI] [PubMed] [Google Scholar]
  54. Pilar G., Landmesser L. Ultrastructural differences during embryonic cell death in normal and peripherally deprived ciliary ganglia. J Cell Biol. 1976 Feb;68(2):339–356. doi: 10.1083/jcb.68.2.339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Rich K. M., Luszczynski J. R., Osborne P. A., Johnson E. M., Jr Nerve growth factor protects adult sensory neurons from cell death and atrophy caused by nerve injury. J Neurocytol. 1987 Apr;16(2):261–268. doi: 10.1007/BF01795309. [DOI] [PubMed] [Google Scholar]
  56. Ruit K. G., Elliott J. L., Osborne P. A., Yan Q., Snider W. D. Selective dependence of mammalian dorsal root ganglion neurons on nerve growth factor during embryonic development. Neuron. 1992 Mar;8(3):573–587. doi: 10.1016/0896-6273(92)90284-k. [DOI] [PubMed] [Google Scholar]
  57. Rydel R. E., Greene L. A. cAMP analogs promote survival and neurite outgrowth in cultures of rat sympathetic and sensory neurons independently of nerve growth factor. Proc Natl Acad Sci U S A. 1988 Feb;85(4):1257–1261. doi: 10.1073/pnas.85.4.1257. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. SLATER T. F., SAWYER B., STRAEULI U. STUDIES ON SUCCINATE-TETRAZOLIUM REDUCTASE SYSTEMS. III. POINTS OF COUPLING OF FOUR DIFFERENT TETRAZOLIUM SALTS. Biochim Biophys Acta. 1963 Nov 8;77:383–393. doi: 10.1016/0006-3002(63)90513-4. [DOI] [PubMed] [Google Scholar]
  59. Savill J., Fadok V., Henson P., Haslett C. Phagocyte recognition of cells undergoing apoptosis. Immunol Today. 1993 Mar;14(3):131–136. doi: 10.1016/0167-5699(93)90215-7. [DOI] [PubMed] [Google Scholar]
  60. Scott I. D., Nicholls D. G. Energy transduction in intact synaptosomes. Influence of plasma-membrane depolarization on the respiration and membrane potential of internal mitochondria determined in situ. Biochem J. 1980 Jan 15;186(1):21–33. doi: 10.1042/bj1860021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Scott S. A., Davies A. M. Inhibition of protein synthesis prevents cell death in sensory and parasympathetic neurons deprived of neurotrophic factor in vitro. J Neurobiol. 1990 Jun;21(4):630–638. doi: 10.1002/neu.480210410. [DOI] [PubMed] [Google Scholar]
  62. Snider W. D., Johnson E. M., Jr Neurotrophic molecules. Ann Neurol. 1989 Oct;26(4):489–506. doi: 10.1002/ana.410260402. [DOI] [PubMed] [Google Scholar]
  63. Sokoloff L., Reivich M., Kennedy C., Des Rosiers M. H., Patlak C. S., Pettigrew K. D., Sakurada O., Shinohara M. The [14C]deoxyglucose method for the measurement of local cerebral glucose utilization: theory, procedure, and normal values in the conscious and anesthetized albino rat. J Neurochem. 1977 May;28(5):897–916. doi: 10.1111/j.1471-4159.1977.tb10649.x. [DOI] [PubMed] [Google Scholar]
  64. Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
  65. Sylvester R. K., Fisher A. J., Lobell M. Cytarabine-induced cerebellar syndrome: case report and literature review. Drug Intell Clin Pharm. 1987 Feb;21(2):177–180. [PubMed] [Google Scholar]
  66. Tanaka S., Koike T. Caffeine promotes survival of cultured sympathetic neurons deprived of nerve growth factor through a cAMP-dependent mechanism. Biochim Biophys Acta. 1992 Dec 15;1175(1):114–122. doi: 10.1016/0167-4889(92)90017-6. [DOI] [PubMed] [Google Scholar]
  67. Tolkovsky A. M., Buckmaster E. A. Deprivation of nerve growth factor rapidly increases purine efflux from cultured sympathetic neurons. FEBS Lett. 1989 Sep 25;255(2):315–320. doi: 10.1016/0014-5793(89)81113-5. [DOI] [PubMed] [Google Scholar]
  68. Umansky S. R. The genetic program of cell death. Hypothesis and some applications: transformation, carcinogenesis, ageing. J Theor Biol. 1982 Aug 21;97(4):591–602. doi: 10.1016/0022-5193(82)90360-5. [DOI] [PubMed] [Google Scholar]
  69. Vistica D. T., Skehan P., Scudiero D., Monks A., Pittman A., Boyd M. R. Tetrazolium-based assays for cellular viability: a critical examination of selected parameters affecting formazan production. Cancer Res. 1991 May 15;51(10):2515–2520. [PubMed] [Google Scholar]
  70. Vogel H., Horoupian D. S. Filamentous degeneration of neurons. A possible feature of cytosine arabinoside neurotoxicity. Cancer. 1993 Feb 15;71(4):1303–1308. doi: 10.1002/1097-0142(19930215)71:4<1303::aid-cncr2820710422>3.0.co;2-6. [DOI] [PubMed] [Google Scholar]
  71. Wallace T. L., Johnson E. M., Jr Cytosine arabinoside kills postmitotic neurons: evidence that deoxycytidine may have a role in neuronal survival that is independent of DNA synthesis. J Neurosci. 1989 Jan;9(1):115–124. doi: 10.1523/JNEUROSCI.09-01-00115.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  72. Winkelman M. D., Hines J. D. Cerebellar degeneration caused by high-dose cytosine arabinoside: a clinicopathological study. Ann Neurol. 1983 Nov;14(5):520–527. doi: 10.1002/ana.410140505. [DOI] [PubMed] [Google Scholar]
  73. Wright L. L., Cunningham T. J., Smolen A. J. Developmental neuron death in the rat superior cervical sympathetic ganglion: cell counts and ultrastructure. J Neurocytol. 1983 Oct;12(5):727–738. doi: 10.1007/BF01258147. [DOI] [PubMed] [Google Scholar]
  74. Wyllie A. H. Glucocorticoid-induced thymocyte apoptosis is associated with endogenous endonuclease activation. Nature. 1980 Apr 10;284(5756):555–556. doi: 10.1038/284555a0. [DOI] [PubMed] [Google Scholar]
  75. Yanagihara K., Tsumuraya M. Transforming growth factor beta 1 induces apoptotic cell death in cultured human gastric carcinoma cells. Cancer Res. 1992 Jul 15;52(14):4042–4045. [PubMed] [Google Scholar]

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