Cell culture research in aging and Alzheimer's disease: The strategic use/reuse of untreated controls and savings people's tax dollars.

IF 2.8 Q2 NEUROSCIENCES
Journal of Alzheimer's disease reports Pub Date : 2025-01-15 eCollection Date: 2025-01-01 DOI:10.1177/25424823241310716
Sudhir Kshirsagar, Md Ariful Islam, Arubala P Reddy, P Hemachandra Reddy
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Abstract

Cell culture is an essential tool in both fundamental and translational research, particularly for understanding complex diseases like Alzheimer's disease (AD). The use of cell lines provides the advantage of genetic homogeneity, ensuring reproducible and consistent results. This article explores the application of mammalian cell cultures to model AD, focusing on the transfection of cells with key genes associated with the disease to replicate the cellular environment of AD. It explains various transfection methods and challenges related to the process. These models offer a robust platform for investigating cellular biology, molecular pathways, physiological processes, and drug discovery efforts. A range of assays, including RT-PCR, western blotting, ELISA, mitochondrial respiration, and reactive oxygen species analysis, are employed to assess the impact of genetic modifications on cellular functions and to screen potential AD therapies. Researchers often design experiments with multiple variables such as genetic modifications, chemical treatments, or time points, paired with positive and negative controls. By using a consistent control group across all conditions and under identical experimental conditions, researchers can minimize variability and enhance data reproducibility. This approach is particularly valuable in AD research, where small experimental differences can significantly influence outcomes. Using a shared control group ensures data comparability across experiments, saving time and resources by eliminating redundant control tests. This strategy not only streamlines the research process but also improves the reliability of results, making it a sensible, resource-efficient method that ultimately conserves public funding in the pursuit of AD treatments.

衰老和阿尔茨海默病的细胞培养研究:未经治疗的对照物的战略性使用/再利用和节省人们的税款。
细胞培养在基础研究和转化研究中都是必不可少的工具,特别是在理解像阿尔茨海默病(AD)这样的复杂疾病方面。细胞系的使用提供了遗传同质性的优势,确保了结果的可重复性和一致性。本文探讨了哺乳动物细胞培养在AD模型中的应用,重点是转染与疾病相关的关键基因细胞,复制AD的细胞环境。它解释了与该过程相关的各种转染方法和挑战。这些模型为研究细胞生物学、分子途径、生理过程和药物发现工作提供了一个强大的平台。包括RT-PCR、western blotting、ELISA、线粒体呼吸和活性氧分析在内的一系列检测方法被用于评估基因修饰对细胞功能的影响,并筛选潜在的AD治疗方法。研究人员经常设计具有多种变量的实验,如基因修饰、化学处理或时间点,并辅以阳性和阴性对照。通过在所有条件和相同的实验条件下使用一致的对照组,研究人员可以最大限度地减少变异性并提高数据的可重复性。这种方法在阿尔茨海默病研究中特别有价值,因为微小的实验差异可以显著影响结果。使用共享控制组可确保实验之间的数据可比性,通过消除冗余的控制测试节省时间和资源。这一策略不仅简化了研究过程,而且提高了结果的可靠性,使其成为一种明智的、资源高效的方法,最终节省了追求阿尔茨海默病治疗的公共资金。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.80
自引率
0.00%
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