TNFα-Related Chondrocyte Inflammation Models: A Systematic Review.

IF 4.9 2区 生物学 International Journal of Molecular Sciences Pub Date : 2024-10-08 DOI:10.3390/ijms251910805
Su Wang, Sarah Kurth, Christof Burger, Dieter C Wirtz, Frank A Schildberg, Robert Ossendorff
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Abstract

Tumor necrosis factor alpha (TNFα), as a key pro-inflammatory cytokine, plays a central role in joint diseases. In recent years, numerous models of TNFα-induced cartilage inflammation have been developed. However, due to the significant differences between these models and the lack of consensus in their construction, it becomes difficult to compare the results of different studies. Therefore, we summarized and compared these models based on important parameters for model construction, such as cell source, cytokine concentration, stimulation time, mechanical stimulation, and more. We attempted to analyze the advantages and disadvantages of each model and provide a compilation of the analytical methods used in previous studies. Currently, TNFα chondrocyte inflammation models can be categorized into four main types: monolayer-based, construct-based, explant-based TNFα chondrocyte inflammation models, and miscellaneous TNFα chondrocyte inflammation models. The most commonly used models were the monolayer-based TNFα chondrocyte inflammation models (42.86% of cases), with 10 ng/mL TNFα being the most frequently used concentration. The most frequently used chondrocyte cell passage is passage 1 (50%). Human tissues were most frequently used in experiments (51.43%). Only five articles included models with mechanical stimulations. We observed variations in design conditions between different models. This systematic review provides the essential experimental characteristics of the available chondrocyte inflammation models with TNFα, and it provides a platform for better comparison between existing and new studies in this field. It is essential to perform further experiments to standardize each model and to find the most appropriate experimental parameters.

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与 TNFα 相关的软骨细胞炎症模型:系统综述。
肿瘤坏死因子α(TNFα)作为一种关键的促炎细胞因子,在关节疾病中发挥着核心作用。近年来,人们建立了许多 TNFα 诱导软骨炎症的模型。然而,由于这些模型之间存在显著差异,且在构建上缺乏共识,因此很难比较不同研究的结果。因此,我们根据构建模型的重要参数,如细胞来源、细胞因子浓度、刺激时间、机械刺激等,对这些模型进行了总结和比较。我们试图分析每种模型的优缺点,并对以往研究中使用的分析方法进行汇编。目前,TNFα软骨细胞炎症模型可分为四大类:单层型、构建型、外植体型TNFα软骨细胞炎症模型和其他TNFα软骨细胞炎症模型。最常用的模型是基于单层的TNFα软骨细胞炎症模型(占42.86%),最常用的TNFα浓度为10纳克/毫升。最常用的软骨细胞通道是通道1(50%)。实验中最常使用的是人体组织(51.43%)。只有五篇文章包含机械刺激模型。我们观察到不同模型的设计条件存在差异。这篇系统性综述提供了现有TNFα软骨细胞炎症模型的基本实验特征,为更好地比较该领域的现有研究和新研究提供了一个平台。我们有必要进行进一步的实验,使每种模型标准化,并找到最合适的实验参数。
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
自引率
10.70%
发文量
13472
审稿时长
1.7 months
期刊介绍: The International Journal of Molecular Sciences (ISSN 1422-0067) provides an advanced forum for chemistry, molecular physics (chemical physics and physical chemistry) and molecular biology. It publishes research articles, reviews, communications and short notes. Our aim is to encourage scientists to publish their theoretical and experimental results in as much detail as possible. Therefore, there is no restriction on the length of the papers or the number of electronics supplementary files. For articles with computational results, the full experimental details must be provided so that the results can be reproduced. Electronic files regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material (including animated pictures, videos, interactive Excel sheets, software executables and others).
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