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血清和钾减少诱导神经元死亡过程中溶酶体组织蛋白酶L和自噬的上调。

Up-regulation of lysosomal cathepsin L and autophagy during neuronal death induced by reduced serum and potassium.

作者信息

Kaasik Allen, Rikk Tiina, Piirsoo Andres, Zharkovsky Tamara, Zharkovsky Alexander

机构信息

Department of Pharmacology, Centre of Excellence for Molecular and Clinical Medicine, University of Tartu, Ravila 19, 51014 Tartu, Estonia.

出版信息

Eur J Neurosci. 2005 Sep;22(5):1023-31. doi: 10.1111/j.1460-9568.2005.04279.x.

DOI:10.1111/j.1460-9568.2005.04279.x
PMID:16176344
Abstract

Serum and potassium deprivation-induced neuronal death on the primary culture of rat cerebellar granule neurons is being widely used as an in vitro model of neurodegeneration and neuronal apoptosis. In our experiments, serum and potassium deprivation for 12 h induced neuronal death in approximately 20% of cerebellar granule neurons as demonstrated by Trypan Blue assay. Neuronal death was accompanied by a transient increase in the intralysosomal cathepsin L activity, which preceded neuronal death. During this time, the lysosomal membrane integrity remained preserved and no leakage of cathepsin L into the cytosol was seen. Ultrastructural analysis revealed the appearance of multiple vacuoles and autophagosomes in the cytoplasmatic compartment of serum- and potassium-deprived granule neurons. Addition of selective cathepsin L inhibitors or of the autophagy inhibitor 3-methyladenine provided partial protection against serum and potassium deprivation-induced death. Our data also show that combining cathepsin L inhibitors and caspase-3 inhibitors leads to a synergistic neuroprotective effect against serum and potassium deprivation. The results of the current study suggest that activation of the autophagosomal--lysosomal compartment plays an important role in neuronal death induced by serum and potassium deprivation in cultured cerebellar granule cells.

摘要

血清和钾离子剥夺诱导大鼠小脑颗粒神经元原代培养物中的神经元死亡,这一现象正被广泛用作神经退行性变和神经元凋亡的体外模型。在我们的实验中,如台盼蓝检测所示,血清和钾离子剥夺12小时可诱导约20%的小脑颗粒神经元死亡。神经元死亡伴随着溶酶体内组织蛋白酶L活性的短暂增加,且该增加先于神经元死亡出现。在此期间,溶酶体膜的完整性得以保留,未观察到组织蛋白酶L泄漏到细胞质中。超微结构分析显示,血清和钾离子剥夺的颗粒神经元细胞质区域出现多个空泡和自噬体。添加选择性组织蛋白酶L抑制剂或自噬抑制剂3-甲基腺嘌呤可部分保护细胞免受血清和钾离子剥夺诱导的死亡。我们的数据还表明,联合使用组织蛋白酶L抑制剂和半胱天冬酶-3抑制剂可产生协同的神经保护作用,对抗血清和钾离子剥夺。当前研究结果表明,自噬体-溶酶体区室的激活在培养的小脑颗粒细胞中血清和钾离子剥夺诱导的神经元死亡中起重要作用。

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