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神经元细胞死亡中的溶酶体系统:综述

The lysosomal system in neuronal cell death: a review.

作者信息

Nixon R A, Cataldo A M

机构信息

Laboratories for Molecular Neuroscience, Mailman Research Center, McLean Hospital, Belmont, Massachusetts 02178.

出版信息

Ann N Y Acad Sci. 1993 May 28;679:87-109. doi: 10.1111/j.1749-6632.1993.tb18291.x.

Abstract

The lysosomal system has often been considered a prominent morphologic marker of distressed or dying neurons. Lysosomes or their constituent hydrolases have been viewed in different neuropathologic states as either initiators and direct agents of cell death, agents of cellular repair and recompensation, effectors of end-stage cellular dissolution, or autolytic scavengers of cellular debris. Limited data and limitations of methodology often do not allow these potential roles to be discriminated. In all forms of neurodegeneration, it may be presumed that lysosomes ultimately rupture and release various hydrolases that promote cell autolysis during the final stages of cellular disintegration. Beyond this perhaps universal contribution to cell death, the degree to which the lysosomal system may be involved in neurodegenerative states varies considerably. In many conditions, morphologic evidence for activation of the lysosomal system is minimal or undetectable. In other cases, lysosomal activation is evident only when other morphologic signs of cell injury are also present. This level of participation may be viewed as either an attempt by the neuron to compensate for or repair the injury or a late-stage event leading to cell dissolution. The early involvement of the lysosomal system in neurodegeneration occurs most commonly in the form of intraneuronal accumulations of abnormal storage profiles or residual bodies (tertiary lysosomes). Very often the lysosomal involvement can be traced to a primary defect or dysfunction of lysosomal components or to accelerated or abnormal membrane breakdown that leads to the buildup of modified digestion-resistant substrates within lysosomes. Because they are often striking, changes in the lysosomal system are a sensitive morphologic indicator of certain types of metabolic distress; however, whether they reflect a salutary response of a compromised neuron or a mechanism to promote cell death and removal of debris from the brain remains to be established for most conditions. Factors that may influence the lysosomal response during lethal neuronal injury include species differences, stage of neuronal development, duration of injury and pace of cell death. The lysosomal system may be more closely coupled to certain forms of neuronal cell death in lower vertebrate or invertebrate systems than in mammalian systems.

摘要

溶酶体系统常被视为受损或濒死神经元的一个显著形态学标志物。在不同的神经病理状态下,溶酶体或其所含的水解酶被视作细胞死亡的启动者和直接动因、细胞修复与代偿的因子、终末期细胞溶解的效应器,或是细胞碎片的自溶清除剂。有限的数据和方法学上的局限常常使得无法区分这些潜在作用。在所有形式的神经退行性变中,可以推测溶酶体最终会破裂并释放各种水解酶,这些水解酶在细胞解体的最后阶段促进细胞自溶。除了对细胞死亡可能具有的这种普遍作用外,溶酶体系统参与神经退行性状态的程度差异很大。在许多情况下,溶酶体系统激活的形态学证据很少或无法检测到。在其他情况下,只有当细胞损伤的其他形态学迹象也存在时,溶酶体激活才明显。这种参与程度可被视为神经元试图补偿或修复损伤,或是导致细胞溶解的晚期事件。溶酶体系统在神经退行性变中的早期参与最常见的形式是神经元内异常储存物质或残余小体(三级溶酶体)的积聚。溶酶体的参与常常可追溯到溶酶体成分的原发性缺陷或功能障碍,或是加速或异常的膜破裂,这导致溶酶体内抗消化底物的积聚。由于溶酶体系统的变化往往很显著,所以它是某些类型代谢应激的敏感形态学指标;然而,在大多数情况下,它们是反映受损神经元的有益反应还是促进细胞死亡及清除脑内碎片的机制,仍有待确定。在致死性神经元损伤期间,可能影响溶酶体反应的因素包括物种差异、神经元发育阶段、损伤持续时间和细胞死亡速度。与哺乳动物系统相比,溶酶体系统在低等脊椎动物或无脊椎动物系统中可能与某些形式的神经元细胞死亡联系更为紧密。

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