首页> 美国卫生研究院文献>Neuroscience Bulletin >Mechanisms of lysosomal proteases participating in cerebral ischemia-induced neuronal death
【2h】

Mechanisms of lysosomal proteases participating in cerebral ischemia-induced neuronal death

机译:溶酶体蛋白酶参与脑缺血性神经元死亡的机制

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

There are three different types of cell death, including apoptosis (Type I), autophagic cell death (Type II), and necrosis (Type III). Ischemic neuronal death influences stroke development and progression. Lysosomes are important organelles having an acidic milieu to maintain cellular metabolism by degrading unneeded extra-and intracellular substances. Lysosomal enzymes, including cathepsins and some lipid hydrolases, when secreted following rupture of the lysosomal membrane, can be very harmful to their environment, which results in pathological destruction of cellular structures. Since lysosomes contain catalytic enzymes for degrading proteins, carbohydrates and lipids, it seems natural that they should participate in cellular death and dismantling. In this review, we discuss the recent developments in ischemic neuronal death, and present the possible molecular mechanisms that the lysosomal enzymes participate in the three different types of cell death in ischemic brain damage. Moreover, the research related to the selective cathepsin inhibitors may provide a novel therapeutic target for treating stroke and promoting recovery.
机译:存在三种不同类型的细胞死亡,包括凋亡(I型),自噬细胞死亡(II型)和坏死(III型)。缺血性神经元死亡影响中风的发展和进展。溶酶体是重要的细胞器,具有酸性环境,可通过降解不需要的细胞外和细胞内物质来维持细胞代谢。溶酶体酶,包括组织蛋白酶和某些脂质水解酶,在溶酶体膜破裂后分泌时,可能对其环境非常有害,从而导致细胞结构的病理破坏。由于溶酶体包含用于降解蛋白质,碳水化合物和脂质的催化酶,因此它们应该参与细胞死亡和拆卸似乎很自然。在这篇综述中,我们讨论了缺血性神经元死亡的最新进展,并提出了溶酶体酶参与缺血性脑损伤的三种不同类型细胞死亡的可能分子机制。而且,与选择性组织蛋白酶抑制剂有关的研究可能为治疗中风和促进康复提供新的治疗靶标。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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