Endlicher René, Kriváková Pavla, Lotkova Halka, Milerová Marie, Drahota Zdenek, Cervinková Zuzana
Department of Physiology, Charles University in Prague, Faculty of Medicine and University Hospital Hradec Králové, Czech Republic.
Acta Medica (Hradec Kralove). 2009;52(2):69-72.
Ca(2+)-induced opening of the mitochondrial permeability transition pore (MPTP) is involved in induction of apoptotic and necrotic processes. We studied sensitivity of MPTP to calcium using the model of Ca(2+)-induced, cyclosporine A-sensitive mitochondrial swelling. Presented data indicate that the extent of mitochondrial swelling (dA520/4 min) induced by addition of 25 microM Ca2+ is seven-fold higher in liver than in heart mitochondria (0.564 +/- 0.08/0.077 +/- 0.01). The extent of swelling induced by 100 microM Ca2+ was in liver tree times higher than in heart mitochondria (0.508 +/- 0.05/ 0.173 +/- 0.02). Cyclosporine A sensitivity showed that opening of the MPTP is involved. We may thus conclude that especially at low Ca2+ concentration heart mitochondria are more resistant to damaging effect of Ca2+ than liver mitochondria. These finding thus support hypothesis that there exist tissue specific strategies of cell protection against induction of the apoptotic and necrotic processes.
钙离子诱导的线粒体通透性转换孔(MPTP)开放参与凋亡和坏死过程的诱导。我们使用钙离子诱导的、环孢素A敏感的线粒体肿胀模型研究了MPTP对钙的敏感性。现有数据表明,添加25微摩尔钙离子诱导的线粒体肿胀程度(dA520/4分钟)在肝脏中比在心脏线粒体中高7倍(0.564±0.08/0.077±0.01)。100微摩尔钙离子诱导的肿胀程度在肝脏中比在心脏线粒体中高3倍(0.508±0.05/0.173±0.02)。环孢素A敏感性表明MPTP的开放参与其中。因此我们可以得出结论,特别是在低钙离子浓度下,心脏线粒体比肝脏线粒体对钙离子的损伤作用更具抗性。这些发现因此支持了这样的假设,即存在针对凋亡和坏死过程诱导的组织特异性细胞保护策略。