摘要
神经细胞死亡的机制仍知之甚少,这已经阻碍了许多当前无法医治的神经退行性疾病治疗的进展。这需要发展新的方法,用高敏感性和细胞解析方法揭露细胞死亡的分子机制。使用遗传性视网膜神经退行性动物模型,我们已经研制或改变了不同的生化检验直接和原位测定钙蛋白酶,聚腺苷二磷酸核糖合酶(PARP)和组蛋白去乙酰化酶(HDAC)。此外,采用原位免疫组化技术检测PKG功能依赖性产物,对cGMP依赖性蛋白激酶(PKG)的酶活性进行了间接评估。联合这些检测方法与原位细胞死亡标记物揭示了紧密的时空关系,提示PKG、HDAC,、PARP和钙蛋白酶活性与神经细胞死亡之间的因果关系。利用不同的药理学和基因的操作,因果关系确实得到了证明。令人意外的是,通过相应表达的增加,代谢活动并没有匹配相应的剧增,突显了在分子水平分析蛋白活性的重要性。上面提及的研究鉴定了许多以前未知的但参与遗传视网膜退化的代谢过程。比较不同的动物视网膜退行模型揭露了酶活性惊人的相似性,暗示了破坏性通路的普遍存在。综合起来,这些发现为神经保护作用提供了许多创新靶点,同样地为治疗遗传性视网膜神经性退行性和中枢神经系统和其它可能部分打开了新的视野。
关键词: 钙蛋白酶,细胞死亡,环磷酸鸟苷,组蛋白去乙酰化酶,聚腺苷二磷酸核糖合酶,原位末端标记法
Current Medicinal Chemistry
Title:Novel In Situ Activity Assays for the Quantitative Molecular Analysis of Neurodegenerative Processes in the Retina
Volume: 21 Issue: 30
Author(s): P.A.R. Ekstrom, M. Ueffing, E. Zrenner and F. Paquet-Durand
Affiliation:
关键词: 钙蛋白酶,细胞死亡,环磷酸鸟苷,组蛋白去乙酰化酶,聚腺苷二磷酸核糖合酶,原位末端标记法
摘要: The mechanisms of neuronal cell death are still only poorly understood, which has hindered the advancement of therapies for many currently untreatable neurodegenerative diseases. This calls for the development of new methods which reveal critical molecular mechanisms of the celldeath machinery with both high sensitivity and cellular resolution. Using animal models for hereditary neurodegeneration in the retina, we have developed or adapted different biochemical assays to determine the enzymatic activities of calpain, poly-ADP-ribose-polymerase (PARP), and histone deacetylase (HDAC) directly and in situ. Additionally, the enzymatic activity of cGMP-dependent protein kinase (PKG) was assessed indirectly using in situ immunohistological techniques to detect PKG-activity-dependent products. Combining these assays with in situ cell death markers revealed close temporospatial correlations, suggesting causal connections between the PKG, HDAC, PARP and calpain activities and neuronal cell death. Using different pharmacological and genetic manipulations, causality could indeed be demonstrated. Surprisingly, the often dramatic rises in metabolic activities didnot match by corresponding increases in expression, highlighting the importance of analyses of protein activities at the cellular level. The above mentioned studies identified a number of metabolic processes previously unknownto be involved in inherited retinal degeneration. Comparing different animal retinal degeneration models uncovered striking similarities in enzymatic activities, suggesting a generality of the destructive pathways. Taken together, these findings provided a number of novel targets for neuroprotection and as such opened up new perspectives for the therapy of hereditary neurodegeneration in the retina and possibly other parts of the central nervous system.
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Ekstrom P.A.R., Ueffing M., Zrenner E. and Paquet-Durand F., Novel In Situ Activity Assays for the Quantitative Molecular Analysis of Neurodegenerative Processes in the Retina, Current Medicinal Chemistry 2014; 21 (30) . https://dx.doi.org/10.2174/0929867321666140601201337
DOI https://dx.doi.org/10.2174/0929867321666140601201337 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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