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Insights on a new path of pre-mitochondrial apoptosis regulation by a glycosaminoglycan mimetic.

机译:通过糖胺聚糖模拟物对线粒体前细胞凋亡调控新途径的见解。

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Lysosomal cathepsins have recently been reported to play crucial roles in the regulation of the mitochondrial death cascade by an unclear mechanism leading to mitochondrial membrane permeabilization. Glycosaminoglycans (GAG) are a family of ionic polysaccharides present at the lysosomal compartment and shown to inhibit lysosomal cathepsin activities. The implication of this family of polysaccharides in the regulation of the pre-mitochondrial death cascade has still not been considered. Here, we demonstrate in a model of skin fibroblasts submitted to oxidative stress that a GAG-mimetic protects the lysosome from membrane disruption, reduces intracellular ROS levels, and inhibits mitochondrial membrane potential collapse, cytochrome c release and caspases-9 and -3 activations without affecting the extrinsic pathway of apoptosis. Heparan sulfate and chondroitin sulfate, but not heparin, showed also protecting effects when assessing key points of the intrinsic pathway of apoptosis. We suggest the existenceof molecular links between endogenous GAGs and the regulation of apoptosis.
机译:最近,据报道溶酶体组织蛋白酶通过不清楚的机制导致线粒体膜通透性,在线粒体死亡级联反应的调节中起关键作用。糖胺聚糖(GAG)是溶酶体区室中的一个离子多糖家族,被证明可抑制溶酶体组织蛋白酶的活性。尚未考虑该多糖家族在线粒体前死亡级联反应调控中的意义。在这里,我们在经受氧化应激的皮肤成纤维细胞模型中证明,GAG模拟物可保护溶酶体免受膜破坏,降低细胞内ROS含量,并抑制线粒体膜电位崩溃,细胞色素c释放以及caspases-9和-3活化影响细胞凋亡的外在途径。当评估细胞凋亡的内在途径的关键点时,硫酸乙酰肝素和硫酸软骨素而不是肝素也显示出保护作用。我们建议内源性GAGs和凋亡的调节之间存在分子联系。

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