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Calpain-mediated cleavage of Atg5 switches autophagy to apoptosis

Yousefi, Shida, Perozzo, Remo, Schmid, Inès, Ziemiecki, Andrew, Schaffner, Thomas, Scapozza, Leonardo, Brunner, Thomas, Simon, Hans-Uwe·2006·Nature Cell Biology
DOI 10.1038/ncb1482
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  1. Levine, B. & Klionsky, D. J. Development by self-digestion: Molecular mechanisms and biological functions of autophagy. Dev. Cell 6, 463–477 (2004). · DOI
  2. Gozuacik, D. & Kimchi, A. Autophagy as a cell death and tumor suppressor mechanism. Oncogene 23, 2891–2906 (2004). · DOI
  3. Blommaart, E. F., Luiken, J. J. & Meijer, A. J. Autophagic proteolysis: control and specificity. Histochem. J. 29, 365–385 (1997). · DOI
  4. Yu, L. et al. Regulation of an ATG7–beclin 1 program of autophagic cell death by caspase-8. Science 304, 1500–1502 (2004). · DOI
  5. Shimizu, S. et al. Role of Bcl-2 family proteins in a non-apoptotic programmed cell death dependent on autophagy genes. Nature Cell Biol. 6, 1221–1228 (2004). · DOI · Paper page
  6. Mizushima, N. et al. Dissection of autophagosome formation using Apg5-deficient mouse embryonic stem cells. J. Cell. Biol. 152, 657–667 (2001). · DOI · Paper page
  7. Goldstein, J. C., Waterhouse, N. J., Juin, P., Evan, G. I. & Green, D. R. The coordinate release of cytochrome c during apoptosis is rapid, complete and kinetically invariant. Nature Cell Biol. 2, 156–162 (2000). · DOI
  8. Simon, H.-U. Neutrophil apoptosis pathways and their modifications in inflammation. Immunol. Rev. 193, 101–110 (2003). · DOI
  9. Gao, G. & Dou, Q. P. N-terminal cleavage of Bax by calpain generates a potent proapoptotic 18-kDa fragment that promotes Bcl-2-independent cytochrome c release and apoptotic cell death. J. Cell Biochem. 80, 53–72 (2000). · DOI
  10. Altznauer, F., Conus, S., Cavalli, A., Folkers, G. & Simon, H.-U. Calpain-1 regulates Bax and subsequent Smac-dependent caspase-3 activation in neutrophil apoptosis. J. Biol. Chem. 279, 5947–5957 (2004). · DOI
  11. Arthur, J. S., Elce, J. S., Hegadorn, C., Williams, K. & Greer, P. A. Disruption of the murine calpain small subunit gene, Capn4: calpain is essential for embryonic development but not for cell growth and division. Mol. Cell. Biol. 20, 4474–4481 (2000). · DOI
  12. Martin, S. J. et al. Early redistribution of plasma membrane phosphatidylserine is a general feature of apoptosis regardless of the initiating stimulus: Inhibition by overexpression of Bcl-2 and Abl. J. Exp. Med. 182, 1545–1556 (1995). · DOI · Paper page
  13. Strasser, A. The role of BH3-only proteins in the immune system. Nature Rev. Immunol. 5, 189–200 (2005). · DOI
  14. Marchenko, N. D., Zaika, A. & Moll, U. M. Death signal-induced localization of p53 protein to mitochondria: A potential role in apoptotic signaling. J. Biol. Chem. 275, 16202–16212 (2000). · DOI
  15. Mihara, M. et al. p53 has a direct apoptogenic role at the mitochondria. Mol. Cell 11, 577–590 (2003). · DOI
  16. Leu, J. I., Dumont, P., Hafey, M., Murphy, M. E. & George, D. L. Mitochondrial p53 activates Bak and causes disruption of a Bak-Mcl1 complex. Nature Cell Biol. 6, 443–450 (2004). · DOI
  17. Li, H. et al. Cytochrome c release and apoptosis induced by mitochondrial targeting of nuclear orphan receptor TR3. Science 289, 1159–1164 (2000). · DOI
  18. Karuman, P. et al. The Peutz-Jegher gene product LKB1 is a mediator of p53-dependent cell death. Mol. Cell 7, 1307–1319 (2001). · DOI
  19. Chua, B. T. et al. Mitochondrial translocation of cofilin is an early step in apoptosis induction. Nature Cell Biol. 5, 1083–1089 (2003). · DOI
  20. Daigle, I., Yousefi, S., Colonna, M., Green, D. R. & Simon, H.-U. Death receptors bind SHP-1 and block cytokine-induced anti-apoptotic signaling in neutrophils. Nature Med. 8, 61–67 (2002). · DOI
  21. Simon, H.-U. et al. Eosinophils maintain their capacity to signal and release eosinophil cationic protein upon repetitive stimulation with the same agonist. J. Immunol. 165, 4069–4075 (2000). · DOI
  22. Altznauer, F. et al. Inflammation-associated cell cycle-independent block of apoptosis by survivin in terminally differentiated neutrophils. J. Exp. Med. 199, 1343–1354 (2004). · DOI
  23. Martinelli, S. et al. Induction of genes mediating interferon-dependent extracellular trap formation during neutrophil differentiation. J. Biol. Chem. 279, 44123–44132 (2004). · DOI
  24. Adrain, C., Creagh, E. M. & Martin, S. J. Apoptosis-associated release of Smac/DIABLO from mitochondria requires active caspases and is blocked by Bcl-2. EMBO J. 20, 6627–6636 (2001). · DOI
  25. Yousefi, S., Green, D. R., Blaser, K. & Simon, H.-U. Protein-tyrosine phosphorylation regulates apoptosis in human eosinophils and neutrophils. Proc. Natl Acad. Sci. USA 91, 10868–10872 (1994). · DOI
  26. von Gunten, S. et al. Siglec-9 transduces apoptotic and nonapoptotic death signals into neutrophils depending on the proinflammatory cytokine environment. Blood 106, 1423–1431 (2005). · DOI
  27. Takeuchi, H., Kanzawa, T., Kondo, Y. & Kondo, S. Inhibition of platelet-derived growth factor signalling induces autophagy in malignant glioma cells. Br. J. Cancer 90, 1069–1075 (2004). · DOI
  28. Wolf, B. B. et al. Calpain functions in a caspase-independent manner to promote apoptosis-like events during platelet activation. Blood 94, 1683–1692 (1999). · DOI
  29. Bovia, F. et al. Efficient transduction of primary human B lymphocytes and nondividing myeloma B cells with HIV-1-derived lentiviral vectors. Blood 101, 1727–1733 (2003). · DOI
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Metadata

Authors
Yousefi, S., Perozzo, R., Schmid, I., Ziemiecki, A., Schaffner, T., Scapozza, L., Brunner, T., & Simon, H.-U.
Venue
Nature Cell Biology
Publisher
Springer Science and Business Media LLC
Published
2006-09-24
Volume
8
Issue
10
Pages
1124-1132
ISSN
  • 1465-7392
  • 1476-4679
DOI
10.1038/ncb1482
Cited by
1,158
References
3
Language
en
Licence
www.springer.com/tdm (tdm)

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