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GD3-7-aldehyde is an apoptosis inducer and interacts with adenine nucleotide translocase
Authors:Catherine Brenner  Bernhard Kniep  Evelyne Maillier  Claudia Franke  Michael Bachmann  Roger Sandhoff
Institution:a University of Versailles-SQY, PRES UniverSud Paris, CNRS UMR8159, 45, Avenue des Etats-Unis, 78035 Versailles, France
b Technical University of Dresden, Institute of Immunology, Medical Faculty Carl Gustav Carus, Fetscherstr. 74, 01307 Dresden, Germany
c German Cancer Research Center, Department of Cellular and Molecular Pathology, Im Neuenheimer Feld 280, 69120 Heidelberg, Germany
Abstract:We prepared GD3-7-aldehyde (GD3-7) and determined its apoptotic potential. GD3-7 proved to be more efficient to induce pro-apoptotic mitochondrial alterations than GD3 when tested on mouse liver mitochondria. GD3-7-induced mitochondrial swelling and depolarization was blocked by cyclosporin A (CsA) supporting a critical role of the permeability transition pore complex (PTPC) during GD3-7-mediated apoptosis. In contrast to GD3, GD3-7 was able to induce channel formation in proteoliposomes containing adenine nucleotide translocase (ANT). This suggests that ANT is the molecular target of GD3-7. Using a specific antiserum, GD3-7 was detected in the lipid extract of the myeloid tumor cell line HL-60 after apoptosis induction, but not in living cells. Therefore, GD3-7 might be a novel mediator of PTPC-dependent apoptosis in cancer cells.
Keywords:amu  atomic mass units  ANT  adenine nucleotide translocase  CAT  carboxyatractyloside  CsA  cyclosporin A  CypD  cyclophilin D  ΔΨm  mitochondrial transmembrane potential  MMP  mitochondrial membrane permeabilization  PT  permeabilty transition  PTPC  permeability transition pore complex  VDAC  voltage-dependent anion channel  4-MUP  4-methyl umbelliferyl phosphate  GM3  II3NeuAc-LacCer  GD3  II3(NeuAc)2-LacCer  GD3-7  GD3-7-aldehyde  AcGD3  9-O-acetyl GD3
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