4.5 Article

EX VIVO INTERVERTEBRAL DISC CULTURES: DEGENERATION-INDUCTION METHODS AND THEIR IMPLICATIONS FOR CLINICAL TRANSLATION

Journal

EUROPEAN CELLS & MATERIALS
Volume 45, Issue -, Pages 88-112

Publisher

AO RESEARCH INSTITUTE DAVOS-ARI
DOI: 10.22203/eCM.v045a07

Keywords

Disc culture; organ culture; explant culture; 3R; low back pain

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Strategies to regenerate or repair intervertebral discs are being explored, and ex vivo disc cultures are frequently used for studying human intervertebral disc degeneration (IVDD). A systematic search of induction methods for degenerative changes revealed five categories and 129 studies. Currently, spontaneously degenerated disc cultures from large animals provide the closest resemblance to human IVDD. Future advancements in disc culture setups may better mimic human IVDD.
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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