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Presence of DNase γ-Like Endonuclease in Nuclei of Neuronal Differentiated PC12 Cells

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Abstract

DNase γ, which cleaves chromosomal DNA into nucleosomal units (DNA ladder formation), has been suggested to be the critical component of apoptotic machinery. Using rat pheochromocytoma PC12 cells, which are differentiated to sympathetic neurons by nerve growth factor (NGF), we investigated whether DNase γ-like enzyme is present in neuronal cells and is involved in neuronal cell death. The nuclear auto-digestion assay for DNase catalyzing internucleosomal DNA cleavage revealed that nuclei from neuronal differentiated PC12 cells contain acidic and neutral endonucleases, while nuclei from undifferentiated PC12 cells have only acidic endonuclease. The DNA ladder formation observed in isolated nuclei from neuronal differentiated PC12 cells at neutral pH requires both Ca2+ and Mg2+, and is sensitive to Zn2+. The molecular mass of the neutral endonuclease present in neuronal differentiated PC12 cell nuclei is 32000 as determined by activity gel analysis (zymography). The properties of the neuronal endonuclease present in neuronal differentiated PC12 cell nuclei were similar to those of purified DNase γ from rat thymocytes and splenocytes. Interestingly, in neuronal differentiated PC12 cells, internucleosomal DNA fragmentation is observed following NGF deprivation, whereas undifferentiated PC12 cells fail to exhibit DNA ladder formation during cell death by serum starvation. These results suggest that the DNase γ-like endonuclease present in neuronal differentiated PC12 cell nuclei is involved in internucleosomal DNA fragmentation during apoptosis, induced by NGF deprivation.

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References

  1. Raff MC, Barres BA, Burne JF, Coles HS, Ishizaki Y, Jacobson MD. Programmed cell death and the control of cell survival: Lessons from the nervous system. Science 1993; 262: 695–700.

    Google Scholar 

  2. Garcia I, Martinou I, Tsujimoto Y, Marrinou JC. Prevention of programmed cell death of sympathetic neurons by the bcl-2 proto-oncogene. Science 1992; 258: 302–304.

    Google Scholar 

  3. Gonzalez-Garcia M, Garcia I, Ding L, O'Shea S, Boise LH, Thompson CB, Nunez G. bcl-x is expressed in embryonic and postnatal neural tissues and functions to prevent neuronal cell death. Proc Natl Acad Sci USA 1995; 92: 4304–4308.

    Google Scholar 

  4. Gagliardini V, Fernandez P-A, Lee RKK, Drexler HCA, Rotello RJ, Fishman MC, Yuan J. Prevention of vertebrate neruronal death by crmA gene. Science 1994; 263: 826–828.

    Google Scholar 

  5. Yao R, Cooper GM. Requirement for phosphatidylinositol-3 kinase in the prevention of apoptosis by nerve growth factor. Science 1995; 267: 2003–2006.

    Google Scholar 

  6. Xia Z, Dickens M, Raingeaud J, Davis RJ, Greenberg ME. Opposing effects of ERK and JNK-p38 MAP kinases on apoptosis. Science 1995; 270: 1326-1331.

    Google Scholar 

  7. Batistatou A, Greene LA. Aurintricarboxylic acid rescues PC 12 cells and sympathetic neurons from cell death caused by nerve growth factor deprivation: correlation with suppression of endonuclease activity. J Cell Biol 1991; 115: 461–471.

    Google Scholar 

  8. Bredesen DE. Neural apoptosis. Ann Neurol 1995; 38: 839–851.

    Google Scholar 

  9. Arends MJ, Morris RG, Wyllie AH. Apoptosis. The role of the endonuclease. Ame J Pathol 1990; 136: 593–608.

    Google Scholar 

  10. Peitsch MC, Mannherz HG, Tschopp J. The apoptosis endonucleases: cleaning up after cell death. Trends Cell Biol 1994; 4: 37–41.

    Google Scholar 

  11. Tanuma S. DNA fragmentation in apoptosis. Tissu Cult Commun 1995; 14: 133–140.

    Google Scholar 

  12. Tanuma S. Molecular mechanism of apoptosis. In: Sluyser M, ed. Apoptosis in Normal Development and Cancer. London: Taylor & Francis Ltd. 1996: 39–59.

    Google Scholar 

  13. Gaido ML, Cidlowski JA. Identification, purification, and characterization of a calcium-dependent endonuclease (NUC18) from apoptotic rat thymocytes. J Biol Chem 1991; 266: 18580–18585.

    Google Scholar 

  14. Peitsch MC, Polzar B, Stephan H, Crompton T, MacDonald HR, Mannherz HG, Tschopp J. Characterization of the endogenous deoxyribonuclease involved in nuclear DNA degradation during apoptosis (programmed cell death). EMBO J 1993; 12: 371–377.

    Google Scholar 

  15. Nikonova LV, Beletsky IP, Umansky SR. Properties of some nuclear nucleases of rat thymocytes and their changes in radiation-induced apoptosis. Eur J Biochem 1993; 215: 893–901.

    Google Scholar 

  16. Ribeiro JM, Carson DA. Ca2+/Mg2+-dependent endonuclease from human spleen: purification, properties and role in apoptosis. Biochemistry 1993; 32: 9129–9136.

    Google Scholar 

  17. Barry MA, Eastman A. Identification of deoxyribonuclease II as an endonuclease involved in apopcosis. Arch Biochem Biophys 1993; 300: 440–450.

    Google Scholar 

  18. Tanuma S, Shiokawa D. Multiple forms of nuclear deoxyribonuclease in rat thymocytes. Biochem Biophys Res Comm 1994; 203: 789–797.

    Google Scholar 

  19. Shiokawa D, Nishimura K, Maruta H, Tanuma S. DNA fragmentation during thymic apoptosis is catalyzed by DNase γ. Apoptosis 1996; 1: 147–152.

    Google Scholar 

  20. Shiokawa D, Ohyama H, Yamada T, Takahashi K, Tanuma S. Identification of an endonuclease responsible for apoptosis in rat thymocyte. Eur J Biochem 1994; 226: 23–30.

    Google Scholar 

  21. Shiokawa D, Ohyama H, Yamada T, Tanuma S. Purification and properties of DNase γ from apoptotic rat thymocytes. Biochem J 1997; 326: 675–681.

    Google Scholar 

  22. Shiokawa D, lwamatsu A, Tanuma S. Purification, characterization, and amino acid sequencing of DNase γ from rat spleen. Arch Biochem Biophys 1997; 346: 15–20.

    Google Scholar 

  23. Oppenheim RW. Cell death during development of the nervous system. Annu Rev Neurosci 1991; 14: 453–501.

    Google Scholar 

  24. Levi-Montalcini R. The nerve growth factor; thirty-five years later. Science 1987; 237: 1154–1162.

    Google Scholar 

  25. Barde Y-A. Torophic factors and neuronal survival. Neuron 1989; 2: 1525–1534.

    Google Scholar 

  26. Edwards SN, Tolkovsky AM. Characterization of apoptosis in cultured rat sympathetic neurons after nerve growth factor withdrawal. J Cell Biol 1994; 124: 537–546.

    Google Scholar 

  27. Batistatou A, Greene LA. Internucleosomal DNA cleavage and neuronal cell survival/death. J Cell Biol 1993; 122: 523–532.

    Google Scholar 

  28. Mesner PW, Winters TR, Green SH. Nerve growth factor withdrawal-induced cell death in neuronal PC12 cells resembles chat in sympathetic neurons. J Cell Biol 1992; 119: 1669–1680.

    Google Scholar 

  29. Laemmli UK. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 1970; 227: 680–685.

    Google Scholar 

  30. Abe H, Tanuma S. Properties of poly(ADP-ribose) glycohydrolase purified from pig testis nuclei. Arch Biochem Biophys 1996; 336: 139–146.

    Google Scholar 

  31. Greene LA, Aletta JM, Rukenstein A, Green SH. PC12 pheochromocytoma cells: culture, nerve growth factor treatment, and experimental exploitation. Metho Enzymol 1987; 147: 207–216.

    Google Scholar 

  32. Kawabata H, Anzai N, Masutani H, Hirama T, Hishita T, Dodo M, Masuda T, Yoshida Y, Okuma M. Mg2+-or Mn2+-dependent endonuclease activities of human myeloid leukemia cells capable of producing nucleosomal-size DNA fragmentation. Biochem Biophys Res Commun 1997; 233: 133–138.

    Google Scholar 

  33. Cohen GM. Caspases: the executioners of apoptosis. Biochem J 1997; 326: 1–16.

    Google Scholar 

  34. Martinou J-C, Sadoul R. ICE-like protease execute the neuronal death program. Curr Opin Neurobiol 1996; 6: 609–614.

    Google Scholar 

  35. Deshmukh M, Vasilakos J, Deckwerth TL, Lampe PA, Shivers BD, Johnson J. Genetic and metabolic status of NGF-deprived sympathetic neurons saved by an inhibitor of ICE family proteases. J Cell Biol 1996; 135: 1341–1354.

    Google Scholar 

  36. Stefanis L, Park DS, Yan CYI, et al. Induction of CPP32-like activity in PC12 cells by withdrawal of trophic support. J Biol Chem 1996; 271: 30663–30671.

    Google Scholar 

  37. Kuida K, Zheng TS, Na S, et al. Decreased apoptosis in the brain and premature lethality in CPP32-deficient mice. Nature 1996; 384: 368–372.

    Google Scholar 

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Nishimura, K., Tanuma, S. Presence of DNase γ-Like Endonuclease in Nuclei of Neuronal Differentiated PC12 Cells. Apoptosis 3, 97–103 (1998). https://doi.org/10.1023/A:1009644924530

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