首页> 外文期刊>Translational Stroke Research >Lysosomal Membrane Permeabilization as a Key Player in Brain Ischemic Cell Death: a “Lysosomocentric” Hypothesis for Ischemic Brain Damage
【24h】

Lysosomal Membrane Permeabilization as a Key Player in Brain Ischemic Cell Death: a “Lysosomocentric” Hypothesis for Ischemic Brain Damage

机译:溶酶体膜通透性是脑缺血性细胞死亡的关键因素:缺血性脑损伤的“溶酶体中心”假说。

获取原文
获取原文并翻译 | 示例
           

摘要

This is a speculative review of the role of the lysosome in ischemic cell death in the mammalian brain. In particular, it focuses on the role of the permeabilization of the lysosomal membrane to proteins (LMP) as a major mechanism of cell death in mild, but lethal, ischemic insults. The first section of the review outlines the evidence that this is the case, using the relatively few extant studies of mammalian brain. In the second section of the review, the mechanism by which an ischemic insult might lead to LMP is discussed. A metabolic sequence including NMDA receptor activation, activation of phospholipase A2 and production of free radicals, and also the activation of calpain are shown to be critical. The remainder of the section speculates on the actual agent(s) which may be causing the lysosomal membrane change, based on extensive literature references. There is currently no knowledge of the actual mechanism. The third section considers potential targets of the released lysosomal proteases and other proteins that might mediate the lethal effects of LMP, focusing largely on the mitochondria as the target. Again, this is speculative as the targets are not known. Finally, the fourth section addresses the level of importance that LMP has in the process of ischemic cell death and concludes that it may well play the major role during mild but lethal ischemic insults. This novel, so-called “lysosomocentric,” hypothesis is briefly critiqued. The therapeutic potential of this conclusion is then discussed.
机译:这是对溶酶体在哺乳动物脑缺血细胞死亡中作用的推测。特别地,它着重于溶酶体膜对蛋白质的透化作用(LMP),作为轻度但致命的缺血性损伤中细胞死亡的主要机制。综述的第一部分使用相对较少的对哺乳动物大脑的研究,概述了这种情况的证据。在本综述的第二部分中,讨论了缺血性损伤可能导致LMP的机制。包括NMDA受体活化,磷脂酶A2活化和自由基产生以及钙蛋白酶的活化的代谢序列被证明是关键的。本节的其余部分根据大量文献参考推测可能导致溶酶体膜改变的实际药物。目前尚不了解实际机制。第三部分考虑了释放的溶酶体蛋白酶和其他可能介导LMP致死作用的蛋白的潜在靶标,主要集中于线粒体作为靶标。同样,这是推测性的,因为目标未知。最后,第四部分论述了LMP在缺血性细胞死亡过程中的重要性水平,并得出结论,它可能在轻度但致命的缺血性损伤中起主要作用。对这种新颖的所谓“溶血同心性”假说进行了简短的批评。然后讨论该结论的治疗潜力。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号