par Suarez Gonzalez, Nathalie 
;Lecocq, Raymond ;Mosselmans, R;Galand, Paul ;Dumont, Jacques Emile ;Robaye, Bernard
Référence Cell proliferation, 33, 2, page (101-114)
Publication Publié, 2000-04
;Lecocq, Raymond ;Mosselmans, R;Galand, Paul ;Dumont, Jacques Emile ;Robaye, Bernard Référence Cell proliferation, 33, 2, page (101-114)
Publication Publié, 2000-04
Article révisé par les pairs
| Résumé : | The cytoskeleton undergoes dramatic changes during apoptosis and many cytoskeletal proteins are known to be degraded during this process. The number of proteases found to be involved in apoptosis is growing but the role of the proteolysis they cause remains poorly understood. This report describes for the first time that myosin heavy chain is cleaved in aortic endothelial cell apoptosis induced either by tumour necrosis factor-alpha or okadaic acid. The cleavage was specific since a well-defined major 97 kDa fragment of myosin heavy chain was produced. The intermediate filament component vimentin was also cleaved into well-defined fragments (31, 28 and 23 kDa). Kinetic studies showed that proteolysis occurred concomitantly with the morphological changes associated with apoptosis, i.e. cellular condensation and fragmentation in apoptotic bodies. These data suggest that the degradation of myosin and vimentin could be involved in the execution of the morphological alterations observed during apoptotic cell death. |
