Ex vivo intervertebral disc cultures: degeneration-induction methods and their implications for clinical translation.

IF 3.2 3区 医学 Q3 CELL & TISSUE ENGINEERING European cells & materials Pub Date : 2023-03-29 DOI:10.22203/eCM.v045a07
E Salzer, T C Schmitz, V Hm Mouser, A Vernengo, B Gantenbein, J U Jansen, C Neidlinger-Wilke, H-J Wilke, S Grad, C L Le Maitre, M A Tryfonidou, K Ito
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Abstract

Because low back pain is frequently a result of intervertebral disc degeneration (IVDD), strategies to regenerate or repair the IVD are currently being investigated. Often, ex vivo disc cultures of non-human IVD organs or tissue explants are used that usually do not exhibit natural IVDD. Therefore, degenerative changes mimicking those reported in human IVDD need to be induced. To support researchers in selecting ex vivo disc cultures, a systematic search was performed for them and their potential use for studying human IVDD reviewed. Five degeneration induction categories (proinflammatory cytokines, injury/damage, degenerative loading, enzyme, and other) were identified in 129 studies across 7 species. Methods to induce degeneration are diverse and can induce mild to severe degenerative changes that progress over time, as described for human IVDD. The induced degenerative changes are model-specific and there is no "one-fits-all" IVDD induction method. Nevertheless, specific aspects of human IVDD can be well mimicked. Currently, spontaneously degenerated disc cultures from large animals capture human IVDD in most aspects. Combinatorial approaches of several induction methods using discs derived from large animals are promising to recapitulate pathological changes on several levels, such as cellular behaviour, extracellular matrix composition, and biomechanical function, and therefore better mimic human IVDD. Future disc culture setups might increase in complexity, and mimic human IVDD even better. As ex vivo disc cultures have the potential to reduce and even replace animal trials, especially during preclinical development, advancement of such models is highly relevant for more efficient and cost-effective clinical translation from bench-to-bedside.

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离体椎间盘培养:退变诱导方法及其对临床翻译的影响。
由于腰痛通常是椎间盘退变(IVDD)的结果,目前正在研究再生或修复IVD的策略。通常,体外培养的非人类IVD器官或组织外植体通常不会表现出自然的IVDD。因此,需要诱导类似人类IVDD报道的退行性改变。为了支持研究人员选择离体圆盘培养物,对它们进行了系统的搜索,并回顾了它们在研究人类IVDD方面的潜在用途。在7个物种的129项研究中确定了5种变性诱导类别(促炎细胞因子、损伤/损伤、变性负荷、酶和其他)。诱导退行性变的方法多种多样,可以诱导轻度到重度的退行性变化,随着时间的推移而进展,正如人类IVDD所描述的那样。诱导的退行性改变是模型特异性的,没有“一刀切”的IVDD诱导方法。然而,人类IVDD的特定方面可以很好地模仿。目前,来自大型动物的自发退变椎间盘培养物在大多数方面捕获了人类IVDD。利用来自大型动物的椎间盘的几种诱导方法的组合方法有望在几个层面上概括病理变化,如细胞行为、细胞外基质组成和生物力学功能,因此可以更好地模拟人类IVDD。未来的光盘培养设置可能会增加复杂性,甚至更好地模拟人类IVDD。由于离体椎间盘培养有可能减少甚至取代动物试验,特别是在临床前开发过程中,因此这种模型的进步与从实验室到床边的更有效和更具成本效益的临床转化高度相关。
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
European cells & materials
European cells & materials 生物-材料科学:生物材料
CiteScore
6.00
自引率
6.50%
发文量
55
审稿时长
1.5 months
期刊介绍: eCM provides an interdisciplinary forum for publication of preclinical research in the musculoskeletal field (Trauma, Maxillofacial (including dental), Spine and Orthopaedics). The clinical relevance of the work must be briefly mentioned within the abstract, and in more detail in the paper. Poor abstracts which do not concisely cover the paper contents will not be sent for review. Incremental steps in research will not be entertained by eCM journal.Cross-disciplinary papers that go across our scope areas are welcomed.
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