, Volume 11, Issue 3, pp 337–346

Prolonged activation of ERK1,2 induces FADD-independent caspase 8 activation and cell death

  • S. Cagnol
  • E. Van Obberghen-Schilling
  • J.-C. Chambard

DOI: 10.1007/s10495-006-4065-y

Cite this article as:
Cagnol, S., Van Obberghen-Schilling, E. & Chambard, JC. Apoptosis (2006) 11: 337. doi:10.1007/s10495-006-4065-y


Prolonged ERK/MAPK activation has been implicated in neuronal cell death in vitro and in vivo. We found that HEK293 cells, recently reported to express neuronal markers, are exquisitely sensitive to long term ERK stimulation. Activation of an inducible form of Raf-1 (Raf-1:ER) in HEK293 cells induced massive apoptosis characterized by DNA degradation, loss of plasma membrane integrity and PARP cleavage. Cell death required MEK activity and protein synthesis and occurred via the death receptor pathway independently of the mitochondrial pathway. Accordingly, prolonged ERK stimulation activated caspase 8 and strongly potentiated Fas signaling. The death receptor adaptator FADD was found to be rapidly induced upon ERK activation. However using RNA interference and ectopic expression, we demonstrated that neither FADD nor Fas were necessary for caspase 8 activation and cell death. These findings reveal that prolonged ERK/MAPK stimulation results in caspase 8 activation and cell death.


apoptosis caspase 8 ERK (MAPK) FADD HEK293 



extracellular-regulated kinase (MAPK)


MAP and ERK kinase (MAP2K)


fas-associated protein with death domain


dominant negative-FADD




Δ-Raf1:ER; 4-HT: 4-hydroxytamoxifen

Copyright information

© Springer Science + Business Media, Inc. 2006

Authors and Affiliations

  • S. Cagnol
    • 1
  • E. Van Obberghen-Schilling
    • 1
  • J.-C. Chambard
    • 1
  1. 1.Institute of Signaling, Developmental Biology and Cancer Research, CNRS UMR6543Université de Nice Sophia-Antipolis, Centre Antoine LacassagneNiceFrance

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