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亲环蛋白A影响下SH-SY5Y神经母细胞瘤细胞中神经退行性变相关基因的差异表达:该酶可能是阿尔茨海默病的触发因素和治疗靶点吗?

Differential Expression of Neurodegeneration-Related Genes in SH-SY5Y Neuroblastoma Cells Under the Influence of Cyclophilin A: Could the Enzyme be a Likely Trigger and Therapeutic Target for Alzheimer's Disease?

作者信息

Pashaei Somayeh, Shabani Sasan, Mohammadi Soheila, Morozova-Roche Ludmilla A, Salari Nader, Rahimi Zohreh, Khodarahmi Reza

机构信息

Department of Clinical Biochemistry, School of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran.

Medical Biology Research Center, Health Technology Institute, Kermanshah University of Medical Sciences, Kermanshah, Iran.

出版信息

Neurochem Res. 2024 Dec 5;50(1):47. doi: 10.1007/s11064-024-04253-2.

DOI:10.1007/s11064-024-04253-2
PMID:39636462
Abstract

The function and mechanism of Cyclophilin A (CypA) in modulating gene expression associated with Alzheimer's disease (AD) remain unclear. This multifunctional protein is found to be elevated in the cerebrospinal fluid (CSF) of individuals at risk for AD. The cytotoxic effects of CypA, including both wild-type and the mutant R55A, were assessed using the MTT assay. Prior to this evaluation, the purified recombinant protein was validated through enzymatic activity assays and western blot analysis. Following treatment with CypA and transient transfection using the CypA construct, real-time PCR (qRT-PCR) and western blotting were conducted to analyze the expression of factors involved in various signaling pathways, with an emphasis on inflammation, cell death, and intercellular communication. The findings indicate that CypA has a significant impact on the gene expression of factors associated with inflammation and the progression of AD in SH-SY5Y cells. It can be concluded that CypA is capable of regulating gene expression in SH-SY5Y cells, either in a manner dependent on or independent of its enzymatic activity. Additionally, the influence of this multifunctional protein on gene expression is contingent upon the specific site of action, as well as the dosage and duration of exposure to the cells.

摘要

亲环蛋白A(CypA)在调节与阿尔茨海默病(AD)相关基因表达中的功能和机制尚不清楚。人们发现这种多功能蛋白在有患AD风险个体的脑脊液(CSF)中含量升高。使用MTT法评估了野生型和突变型R55A的CypA的细胞毒性作用。在进行该评估之前,通过酶活性测定和蛋白质免疫印迹分析对纯化的重组蛋白进行了验证。在用CypA处理并使用CypA构建体进行瞬时转染后,进行实时定量聚合酶链反应(qRT-PCR)和蛋白质免疫印迹分析,以分析参与各种信号通路的因子的表达,重点是炎症、细胞死亡和细胞间通讯。研究结果表明,CypA对SH-SY5Y细胞中与炎症和AD进展相关因子的基因表达有显著影响。可以得出结论,CypA能够在SH-SY5Y细胞中调节基因表达,其方式可能依赖或不依赖于其酶活性。此外,这种多功能蛋白对基因表达的影响取决于具体作用位点,以及对细胞的剂量和暴露持续时间。

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本文引用的文献

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NLRP3 inflammasome signalling in Alzheimer's disease.NLRP3 炎性小体在阿尔茨海默病中的作用机制。
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Inhibitors of Cyclophilin A: Current and Anticipated Pharmaceutical Agents for Inflammatory Diseases and Cancers.亲环素 A 抑制剂:用于治疗炎症性疾病和癌症的现有和预期药物制剂。
Molecules. 2024 Mar 11;29(6):1235. doi: 10.3390/molecules29061235.
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p38-MAPK and CDK5, signaling pathways in neuroinflammation: a potential therapeutic intervention in Alzheimer's disease?
p38丝裂原活化蛋白激酶和细胞周期蛋白依赖性激酶5,神经炎症中的信号通路:对阿尔茨海默病的一种潜在治疗干预?
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Targeting Cyclophilin A and CD147 to Inhibit Replication of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and SARS-CoV-2-Induced Inflammation.靶向亲环素 A 和 CD147 抑制严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)及其诱导的炎症的复制。
Mol Pharmacol. 2023 Dec;104(6):239-254. doi: 10.1124/molpharm.122.000587. Epub 2023 Oct 12.
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Cyclophilin A as a Pro-Inflammatory Factor Exhibits Embryotoxic and Teratogenic Effects during Fetal Organogenesis.亲环素 A 作为一种促炎因子,在胎儿器官发生期表现出胚胎毒性和致畸作用。
Int J Mol Sci. 2023 Jul 10;24(14):11279. doi: 10.3390/ijms241411279.
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Role of neuroinflammation in neurodegeneration development.神经炎症在神经退行性变发展中的作用。
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The potential roles of ATF family in the treatment of Alzheimer's disease.ATF 家族在阿尔茨海默病治疗中的潜在作用。
Biomed Pharmacother. 2023 May;161:114544. doi: 10.1016/j.biopha.2023.114544. Epub 2023 Mar 17.
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The complex genetic architecture of Alzheimer's disease: novel insights and future directions.阿尔茨海默病的复杂遗传结构:新的见解和未来方向。
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Oxidative Stress and Antioxidants in Neurodegenerative Disorders.神经退行性疾病中的氧化应激与抗氧化剂
Antioxidants (Basel). 2023 Feb 18;12(2):517. doi: 10.3390/antiox12020517.
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Mechanistic and therapeutic role of NLRP3 inflammasome in the pathogenesis of Alzheimer's disease.NLRP3炎性小体在阿尔茨海默病发病机制中的作用机制及治疗作用
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