Institute of Science and Technology in Medicine, Keele University, Keele ST55BG, UK.
J Theor Biol. 2011 Nov 21;289:136-50. doi: 10.1016/j.jtbi.2011.08.007. Epub 2011 Aug 22.
Autologous Chondrocyte Implantation (ACI) is a cell-based therapy used mainly for the treatment of chondral defects in the knee. It involves surgically inserting isolated chondrocytes or mesenchymal stem cells (MSCs), previously expanded in culture, into the defect region. These chondrocytes then proliferate and migrate in the process forming extracellular matrix (ECM) and new cartilage. In the case of MSCs, the process of forming new cartilage is initiated only after differentiation of the stem cells into chondrocytes. Many details of the repair process following insertion in humans are unknown. To enable better understanding of the repair process, we present a mathematical model of cartilage regeneration after cell therapy. The key mechanisms involved in the regeneration process are simulated by modelling cell migration, proliferation and differentiation, nutrient diffusion and depletion, and ECM synthesis and degradation at the defect site, both spatially and temporally. The model successfully simulates the progression of cartilage regeneration. The model predicts a time frame of about 18months for the defect to reach full maturation which corresponds with results from clinical studies and demonstrates that cartilage regeneration is a slow process. Moreover, the model also suggests that regeneration using stem cells alone is no better than that using chondrocytes. The stem cells need to first differentiate into chondrocytes before forming ECM and new cartilage, a process that is initiated only after the stem cell density exceeds a threshold value. Furthermore, with chondrocytes alone, the matrix seems to develop from the subchondral bone interface as compared to the normal cartilage interface, in the case of stem cells alone. The influence of initial conditions and parameters, such as the initial cell seeding densities and cell proliferation rates, is shown to not significantly influence the general evolution characteristics other than accelerating the initial growth process. The model presented here is a first approach towards better understanding of cartilage regeneration after cell therapy techniques.
自体软骨细胞植入术(ACI)是一种主要用于治疗膝关节软骨缺损的细胞疗法。它涉及通过手术将分离的软骨细胞或间充质干细胞(MSCs),在培养中预先扩增,插入到缺损区域。这些软骨细胞随后在增殖和迁移过程中形成细胞外基质(ECM)和新的软骨。在 MSCs 的情况下,只有在干细胞分化为软骨细胞后,才开始形成新软骨的过程。在人类中,插入后修复过程的许多细节尚不清楚。为了更好地理解修复过程,我们提出了一种细胞治疗后软骨再生的数学模型。通过模拟细胞迁移、增殖和分化、营养物质扩散和消耗以及 ECM 在缺陷部位的合成和降解的关键机制,该模型在时空上对再生过程进行了模拟。该模型成功地模拟了软骨再生的进展。该模型预测缺陷需要大约 18 个月才能完全成熟,这与临床研究的结果相对应,并表明软骨再生是一个缓慢的过程。此外,该模型还表明,单独使用干细胞的再生效果并不优于使用软骨细胞。干细胞需要先分化为软骨细胞,然后才能形成 ECM 和新软骨,这个过程只有在干细胞密度超过阈值后才会开始。此外,仅使用软骨细胞,基质似乎是从软骨下骨界面而不是正常软骨界面发展的,而单独使用干细胞时则是从软骨下骨界面发展的。结果表明,初始条件和参数(如初始细胞接种密度和细胞增殖率)的影响除了加速初始生长过程外,对一般演化特征没有显著影响。本文提出的模型是更好地理解细胞治疗技术后软骨再生的第一步。