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甄别手术诱导 OA 小鼠模型的时空疾病模式。

Discerning the spatio-temporal disease patterns of surgically induced OA mouse models.

机构信息

Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Department of Traumatology and Reconstructive Surgery, Berlin, Germany.

Computational Medicine, Dep. of Numerical Mathematics, Konrad Zuse Institute, Berlin, Germany.

出版信息

PLoS One. 2019 Apr 11;14(4):e0213734. doi: 10.1371/journal.pone.0213734. eCollection 2019.

Abstract

Osteoarthritis (OA) is the most common cause of disability in ageing societies, with no effective therapies available to date. Two preclinical models are widely used to validate novel OA interventions (MCL-MM and DMM). Our aim is to discern disease dynamics in these models to provide a clear timeline in which various pathological changes occur. OA was surgically induced in mice by destabilisation of the medial meniscus. Analysis of OA progression revealed that the intensity and duration of chondrocyte loss and cartilage lesion formation were significantly different in MCL-MM vs DMM. Firstly, apoptosis was seen prior to week two and was narrowly restricted to the weight bearing area. Four weeks post injury the magnitude of apoptosis led to a 40-60% reduction of chondrocytes in the non-calcified zone. Secondly, the progression of cell loss preceded the structural changes of the cartilage spatio-temporally. Lastly, while proteoglycan loss was similar in both models, collagen type II degradation only occurred more prominently in MCL-MM. Dynamics of chondrocyte loss and lesion formation in preclinical models has important implications for validating new therapeutic strategies. Our work could be helpful in assessing the feasibility and expected response of the DMM- and the MCL-MM models to chondrocyte mediated therapies.

摘要

骨关节炎(OA)是老龄化社会中最常见的致残原因,目前尚无有效的治疗方法。两种临床前模型被广泛用于验证新的 OA 干预措施(MCL-MM 和 DMM)。我们的目的是辨别这些模型中的疾病动态,提供一个明确的时间表,其中各种病理变化发生。通过内侧半月板不稳定术在小鼠中诱导 OA。对 OA 进展的分析表明,软骨细胞丢失和软骨损伤形成的强度和持续时间在 MCL-MM 与 DMM 之间有显著差异。首先,在第 2 周之前就出现了细胞凋亡,并且仅局限于负重区域。损伤后 4 周,凋亡的幅度导致非钙化区软骨细胞减少 40-60%。其次,细胞丢失的进展在空间和时间上先于软骨的结构变化。最后,虽然两种模型中的蛋白聚糖丢失相似,但只有在 MCL-MM 中才更明显地发生 II 型胶原降解。临床前模型中软骨细胞丢失和损伤形成的动态对验证新的治疗策略具有重要意义。我们的工作有助于评估 DMM 和 MCL-MM 模型对软骨细胞介导的治疗的可行性和预期反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8090/6459499/9b8f082f9d2d/pone.0213734.g001.jpg

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