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首页> 外文期刊>Journal of Mathematical Biology >Mathematical modelling of cytokines, MMPs and fibronectin fragments in osteoarthritic cartilage
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Mathematical modelling of cytokines, MMPs and fibronectin fragments in osteoarthritic cartilage

机译:骨关节炎软骨中细胞因子,MMP和纤连蛋白片段的数学建模

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Osteoarthritis (OA) is a degenerative disease which causes pain and stiffness in joints. OA progresses through excessive degradation of joint cartilage, eventually leading to significant joint degeneration and loss of function. Cytokines, a group of cell signalling proteins, present in raised concentrations in OA joints, can be classified into pro-inflammatory and anti-inflammatory groups. They mediate cartilage degradation through several mechanisms, primarily the up-regulation of matrix metalloproteinases (MMPs), a group of collagen-degrading enzymes. In this paper we show that the interactions of cytokines within cartilage have a crucial role to play in OA progression and treatment. We develop a four-variable ordinary differential equation model for the interactions between pro- and anti-inflammatory cytokines, MMPs and fibronectin fragments (Fn-fs), a by-product of cartilage degradation and up-regulator of cytokines. We show that the model has four classes of dynamic behaviour: homoeostasis, bistable inflammation, tristable inflammation and persistent inflammation. We show that positive and negative feedbacks controlling cytokine production rates can determine either a pre-disposition to OA or initiation of OA. Further, we show that manipulation of cytokine, MMP and Fn-fs levels can be used to treat OA, but we suggest that multiple treatment targets may be essential to halt or slow disease progression.
机译:骨关节炎(OA)是一种退行性疾病,导致关节疼痛和僵硬。 OA通过过度降解关节软骨,最终导致显着的关节退化和功能丧失。细胞因子,一种在OA关节中升高浓度的细胞信号传导蛋白可以分为促炎和抗炎组。它们通过几种机制介导软骨降解,主要是基质金属蛋白酶(MMP)的上调,一组胶原降解酶。在本文中,我们表明软骨内细胞因子在OA进展和治疗中的作用具有至关重要的作用。我们开发了一种四变量常分方程模型,用于抗炎细胞因子,MMP和纤连蛋白片段(FN-FS)之间的相互作用,软骨降解和细胞因子上升调节剂的副产物。我们表明该模型具有四种动态行为:同性恋,双稳态炎症,刺激性炎症和持续炎症。我们表明,控制细胞因子生产率的阳性和负反馈可以确定对OA的预处理或OA的开始。此外,我们表明,可以使用细胞因子,MMP和FN-FS水平的操纵来治疗OA,但我们表明多种治疗靶点可能是停止或缓慢疾病进展至关重要。

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