TY - JOUR
T1 - Progressive stages of mitochondrial destruction caused by cell toxic bile salts
AU - Schulz, Sabine
AU - Schmitt, Sabine
AU - Wimmer, Ralf
AU - Aichler, Michaela
AU - Eisenhofer, Sabine
AU - Lichtmannegger, Josef
AU - Eberhagen, Carola
AU - Artmann, Renate
AU - Tookos, Ferenc
AU - Walch, Axel
AU - Krappmann, Daniel
AU - Brenner, Catherine
AU - Rust, Christian
AU - Zischka, Hans
N1 - Funding Information:
The authors declare that no conflict of interest exists and would like to thank Drs. E.E. Rojo, S. Hohenester and S. Müller for their very helpful discussions and D. Wartini and B. Ledermann for their excellent technical support. This study was supported by the Deutsche Forschungsgemeinschaft (DFG) grant RU742/6-1 to CR and HZ.
PY - 2013/6/27
Y1 - 2013/6/27
N2 - The cell-toxic bile salt glycochenodeoxycholic acid (GCDCA) and taurochenodeoxycholic acid (TCDCA) are responsible for hepatocyte demise in cholestatic liver diseases, while tauroursodeoxycholic acid (TUDCA) is regarded hepatoprotective. We demonstrate the direct mitochondrio-toxicity of bile salts which deplete the mitochondrial membrane potential and induce the mitochondrial permeability transition (MPT). The bile salt mediated mechanistic mode of destruction significantly differs from that of calcium, the prototype MPT inducer. Cell-toxic bile salts initially bind to the mitochondrial outer membrane. Subsequently, the structure of the inner boundary membrane disintegrates. And it is only thereafter that the MPT is induced. This progressive destruction occurs in a dose- and time-dependent way. We demonstrate that GCDCA and TCDCA, but not TUDCA, preferentially permeabilize liposomes containing the mitochondrial membrane protein ANT, a process resembling the MPT induction in whole mitochondria. This suggests that ANT is one decisive target for toxic bile salts. To our knowledge this is the first report unraveling the consecutive steps leading to mitochondrial destruction by cell-toxic bile salts.
AB - The cell-toxic bile salt glycochenodeoxycholic acid (GCDCA) and taurochenodeoxycholic acid (TCDCA) are responsible for hepatocyte demise in cholestatic liver diseases, while tauroursodeoxycholic acid (TUDCA) is regarded hepatoprotective. We demonstrate the direct mitochondrio-toxicity of bile salts which deplete the mitochondrial membrane potential and induce the mitochondrial permeability transition (MPT). The bile salt mediated mechanistic mode of destruction significantly differs from that of calcium, the prototype MPT inducer. Cell-toxic bile salts initially bind to the mitochondrial outer membrane. Subsequently, the structure of the inner boundary membrane disintegrates. And it is only thereafter that the MPT is induced. This progressive destruction occurs in a dose- and time-dependent way. We demonstrate that GCDCA and TCDCA, but not TUDCA, preferentially permeabilize liposomes containing the mitochondrial membrane protein ANT, a process resembling the MPT induction in whole mitochondria. This suggests that ANT is one decisive target for toxic bile salts. To our knowledge this is the first report unraveling the consecutive steps leading to mitochondrial destruction by cell-toxic bile salts.
KW - Bile salts
KW - Cholestasis
KW - Liver
KW - Mitochondria
KW - Mitochondrial permeability transition
UR - http://www.scopus.com/inward/record.url?scp=84879234547&partnerID=8YFLogxK
U2 - 10.1016/j.bbamem.2013.05.007
DO - 10.1016/j.bbamem.2013.05.007
M3 - Article
C2 - 23685124
AN - SCOPUS:84879234547
SN - 0005-2736
VL - 1828
SP - 2121
EP - 2133
JO - Biochimica et Biophysica Acta - Biomembranes
JF - Biochimica et Biophysica Acta - Biomembranes
IS - 9
ER -