TY - JOUR
T1 - Caspases disrupt mitochondrial membrane barrier function
AU - Marzo, Isabel
AU - Susin, Santos A.
AU - Petit, Patrice X.
AU - Ravagnan, Luigi
AU - Brenner, Catherine
AU - Larochette, Nathanael
AU - Zamzami, Naoufal
AU - Kroemer, Guido
N1 - Funding Information:
We thank Drs. N. Thornberry (Merck, Rahway, NJ, USA) for recombinant caspases 1, 2, and 4 and Dr. G. Salvesen (The Burnham Institute, La Jolla, CA, USA) for caspases 3 and 6. This work has been supported by grants from the ANRS, ARC, CNRS, FRM, INSERM, LFC (to G.K.). I. Marzo and S.A. Susin receive fellowships from the Spanish Ministry of Science and from the European Commission, respectively.
PY - 1998/5/8
Y1 - 1998/5/8
N2 - Mitochondrial intermembrane proteins including cytochrome c are known to activate caspases. Accordingly, a disruption of the mitochondrial membrane barrier function with release of cytochrome into the cytosol has been shown to precede caspase activation in a number of different models of apoptosis. Here, we addressed the question of whether caspases themselves can affect mitochondrial membrane function. Recombinant caspases were added to purified mitochondria and were found to affect the permeability of both mitochondrial membranes. Thus, caspases cause a dissipation of the mitochondrial inner transmembrane potential. In addition, caspases cause intermembrane proteins including cytochrome c and AIF (apoptosis-inducing factor) to be released through the outer mitochondrial membrane. These observations suggest that caspases and mitochondria can engage in a circular self-amplification loop. An increase in mitochondrial membrane permeability would cause the release of caspase activators, and caspases, once activated, would in turn increase the mitochondrial membrane permeability. Such a self-amplifying system could accelerate the apoptotic process and/or coordinate the apoptotic response between different mitochondria within the same cell.
AB - Mitochondrial intermembrane proteins including cytochrome c are known to activate caspases. Accordingly, a disruption of the mitochondrial membrane barrier function with release of cytochrome into the cytosol has been shown to precede caspase activation in a number of different models of apoptosis. Here, we addressed the question of whether caspases themselves can affect mitochondrial membrane function. Recombinant caspases were added to purified mitochondria and were found to affect the permeability of both mitochondrial membranes. Thus, caspases cause a dissipation of the mitochondrial inner transmembrane potential. In addition, caspases cause intermembrane proteins including cytochrome c and AIF (apoptosis-inducing factor) to be released through the outer mitochondrial membrane. These observations suggest that caspases and mitochondria can engage in a circular self-amplification loop. An increase in mitochondrial membrane permeability would cause the release of caspase activators, and caspases, once activated, would in turn increase the mitochondrial membrane permeability. Such a self-amplifying system could accelerate the apoptotic process and/or coordinate the apoptotic response between different mitochondria within the same cell.
KW - Caspase
KW - Mitochondrion
KW - Permeability transition
KW - Programmed cell death
UR - http://www.scopus.com/inward/record.url?scp=0032496401&partnerID=8YFLogxK
U2 - 10.1016/S0014-5793(98)00424-4
DO - 10.1016/S0014-5793(98)00424-4
M3 - Article
C2 - 9607311
AN - SCOPUS:0032496401
SN - 0014-5793
VL - 427
SP - 198
EP - 202
JO - FEBS Letters
JF - FEBS Letters
IS - 2
ER -