GD3 ganglioside directly targets mitochondria in a bcl-2-controlled fashion.
Rippo, M R ; Malisan, F ; Ravagnan, L ; et al. ; - ASI Sponsor
Oct - 2000
ISSN : 0892-6638 ;
journal : FASEB journal : official publication of the Federation of American Societies for Experimental Biology

Issue : 13
type: Article Journal

Abstract
Lipid and glycolipid diffusible mediators are involved in the intracellular progression and amplification of apoptotic signals. GD3 ganglioside is rapidly synthesized from accumulated ceramide after the clustering of death-inducing receptors and triggers apoptosis. Here we show that GD3 induces dissipation of DeltaPsim and swelling of isolated mitochondria, which results in the mitochondrial release of cytochrome c, apoptosis inducing factor, and caspase 9. Soluble factors released from GD3-treated mitochondria are sufficient to trigger DNA fragmentation in isolated nuclei. All these effects can be blocked by cyclosporin A, suggesting that GD3 is acting at the level of the permeability transition pore complex. We found that endogenous GD3 accumulates within mitochondria of cells undergoing apoptosis after ceramide exposure. Accordingly, suppression of GD3 synthase (ST8) expression in intact cells substantially prevents ceramide-induced DeltaPsim dissipation, indicating that endogenously synthesized GD3 induces mitochondrial changes in vivo. Finally, enforced expression of bcl-2 significantly prevents GD3-induced mitochondrial changes, caspase 9 activation, and apoptosis. These results show that mitochondria are a key destination for apoptogenic GD3 ganglioside along the lipid pathway to programmed cell death and indicate that relevant GD3 targets are under bcl-2 control.

keywords : Animals,Apoptosis,Caspase 9,Caspases,Caspases: metabolism,Cyclosporine,Cyclosporine: pharmacology,Enzyme Activation,Gangliosides,Gangliosides: pharmacology,Liver,Liver: drug effects,Membrane Potentials,Membrane Potentials: drug effects,Mitochondria,Proto-Oncogene Proteins c-bcl-2,Proto-Oncogene Proteins c-bcl-2: biosynthesis,Rats,Sialyltransferases,Sialyltransferases: metabolism,Subcellular Fractions,Subcellular Fractions: drug effects