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Glyceraldehyde-3-Phosphate, a Glycolytic Intermediate, Prevents Cells from Apoptosis by Lowering S-Nitrosylation of Glyceraldehyde-3-Phosphate Dehydrogenase

  • Received : 2011.10.05
  • Accepted : 2011.12.02
  • Published : 2012.04.28

Abstract

Glyceraldehyde-3-phosphate (G-3-P), the substrate of glyceraldehyde-3-phosphate dehydrogenase (GAPDH), is a key intermediate in several metabolic pathways. Recently, we reported that G-3-P directly inhibits caspase-3 activity in a reversible noncompetitive mode, suggesting the intracellular G-3-P level as a cell fate decision factor. It has been known that apoptotic stimuli induce the generation of NO, and NO S-nitrosylates GAPDH at the catalytic cysteine residue, which confers GAPDH the ability to bind to Siah-1, an E3 ubiquitin ligase. The GAPDH-Siah-1 complex is translocated into the nucleus and subsequently triggers the apoptotic process. Here, we clearly showed that intracellular G-3-P protects GAPDH from S-nitrosylation at above a certain level, and consequently maintains the cell survival. In case G-3-P drops below a certain level as a result of exposure to specific stimuli, G-3-P cannot inhibit S-nitrosylation of GAPDH anymore, and consequently GAPDH translocates with Siah-1 into the nucleus. Based on these results, we suggest that G-3-P functions as a molecule switch between cell survival and apoptosis by regulating S-nitrosylation of GAPDH.

Keywords

References

  1. Bao, Q. and Y. Shi. 2007. Apoptosome: A platform for the activation of initiator caspases. Cell Death Diff. 14: 56-65. https://doi.org/10.1038/sj.cdd.4402028
  2. Brown, G. C. 2010. Nitric oxide and neuronal death. Nitric Oxide 23: 153-165. https://doi.org/10.1016/j.niox.2010.06.001
  3. Chuang, D.-M., C. Hough, and V. V. Senatorov. 2005. Glyceraldehyde-3-phosphate dehydrogenase, apoptosis, and neurodegenerative diseases. Annu. Rev. Pharmacol. Toxicol. 45: 269-290. https://doi.org/10.1146/annurev.pharmtox.45.120403.095902
  4. Hara, M. R., M. B. Cascio, and A. Sawa. 2006. GAPDH as a sensor of NO stress. Biochim. Biophys. Acta 1762: 502-509. https://doi.org/10.1016/j.bbadis.2006.01.012
  5. Hara, M. R., B. Thomas, M. B. Cascio, B.-I. Bae, L. D. Hester, V. L. Dawson, et al. 2006. Neuroprotection by pharmacological blockade of the GAPDH death cascade. Proc. Natl. Acad. Sci. USA 103: 3887-3889. https://doi.org/10.1073/pnas.0511321103
  6. Ishitani, R., K. Sunaga, A. Hirano, P. Saunders, N. Katsube, M. Tanaka, and D. M. Chuang. 1996. Evidence that glyceraldehyde-3-phosphate dehydrogenase is involved in age-induced apoptosis in mature cerebellar granule neurons in culture. J. Neurochem. 66: 928-935.
  7. Jang, M., H. J. Kang, S. Y. Lee, S. J. Chung, S. Kang, S. W. Chi, et al. 2009. Glyceraldehyde-3-phosphate, a glycolytic intermediate, plays a key role in controlling cell fate via inhibition of caspase activity. Mol. Cells 28: 559-563. https://doi.org/10.1007/s10059-009-0151-7
  8. Jang, M., B. C. Park, S. Kang, S.-W. Chi, S. Cho, S. J. Chung, et al. 2009. Far upstream element-binding protein-1, a novel caspase substrate, acts as a cross-talker between apoptosis and the c-myc oncogene. Oncogene 28: 1529-1536. https://doi.org/10.1038/onc.2009.11
  9. Kim, E. Y., T.-S. Yoon, Y. J. Bahn, D. G. Jeong, M. R. Park, S. J. Chung, et al. 2010. Proteomic analysis of oxidative stress-induced neuronal cell death by two-dimensional fluorescence difference gel electrophoresis. Int. J. Mol. Med. 26: 829-835.
  10. Kumar, S. 2007. Caspase function in programmed cell death. Cell Death Diff. 14: 32-43. https://doi.org/10.1038/sj.cdd.4402060
  11. Li, C., Z. Xiao, X. Zhang, J. Li, X. Li, H. Yi, et al. 2006. Proteome analysis of human lung squamous carcinoma. Proteomics 6: 547-558. https://doi.org/10.1002/pmic.200500256
  12. Nicholls, C., H. Li, and J. P. Liu. 2011. GAPDH: A common enzyme with uncommon functions. DOI: 10.1111/j.1440-1681.2011.05599.x.
  13. Sen, N., M. R. Hara, M. D. Kornberg, M. B. Cascio, B.-I. Bae, N. Shahani, et al. 2008. Nitric oxide-induced nuclear GAPDH activates p300/CBP and mediates apoptosis. Nature Cell Biol. 10: 866-873. https://doi.org/10.1038/ncb1747
  14. Shahani, N. and A. Sawa. 2011. Nitric oxide signaling and nitrosative stress in neurons: Role for S-nitrosylation. Antioxid. Redox Signal. 14: 1493-1504. https://doi.org/10.1089/ars.2010.3580
  15. Tristan, C., N. Shahani, T. W. Sedlak, and A. Sawa. 2011. The diverse functions of GAPDH: Views from different subcellular compartments. Cell Signal. 23: 317-323. https://doi.org/10.1016/j.cellsig.2010.08.003

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