Voiland School of Chemical Engineering and Bioengineering, Washington State University, 1505 NE Stadium Way, Pullman, WA, 99164-6515, USA.
Department of Biomedical Engineering and Chemical Engineering, The University of Texas at San Antonio, San Antonio, TX, 78249, USA.
In Vitro Cell Dev Biol Anim. 2021 Jun;57(6):631-640. doi: 10.1007/s11626-021-00592-4. Epub 2021 Jun 15.
Conventional treatments of osteoarthritis have failed to re-build functional articular cartilage. Tissue engineering clinical treatments for osteoarthritis, including autologous chondrocyte implantation, provides an alternative approach by injecting a cell suspension to fill lesions within the cartilage in osteoarthritic knees. The success of chondrocyte implantation relies on the availability of chondrogenic cell lines, and their resilience to high mechanical loading. We hypothesize we can reduce the numbers of human articular chondrocytes necessary for a treatment by supplementing cultures with human adipose-derived stem cells, in which stem cells will have protective and stimulatory effects on mixed cultures when exposed to high mechanical loads, and in which coculture will enhance production of requisite extracellular matrix proteins over those produced by stretched chondrocytes alone. In this work, adipose-derived stem cells and articular chondrocytes were cultured separately or cocultivated at ratios of 3:1, 1:1, and 1:3 in static plates or under excessive cyclic tensile strain of 10% and results were compared to culturing of both cell types alone with and without cyclic strain. Results indicate 75% of chondrocytes in engineered articular cartilage can be replaced with stem cells with enhanced collagen over all culture conditions and glycosaminoglycan content over stretched cultures of chondrocytes. This can be done without observing adverse effects on cell viability. Collagen and glycosaminoglycan secretion, when compared to chondrocyte alone under 10% strain, was enhanced 6.1- and 2-fold, respectively, by chondrocytes cocultivated with stem cells at a ratio of 1:3.
常规的骨关节炎治疗方法未能重建功能关节软骨。组织工程学治疗骨关节炎的临床方法,包括自体软骨细胞移植,通过注射细胞悬液为骨关节炎膝关节内的软骨病变提供了一种替代方法。软骨细胞移植的成功依赖于软骨细胞系的可用性及其对高机械负荷的弹性。我们假设通过用人脂肪来源的干细胞补充培养物,可以减少治疗所需的人关节软骨细胞的数量,其中干细胞在暴露于高机械负荷时对混合培养物具有保护和刺激作用,并且共培养物将增强必需的细胞外基质蛋白的产生,超过单独拉伸的软骨细胞产生的量。在这项工作中,将脂肪来源的干细胞和关节软骨细胞分别培养或以 3:1、1:1 和 1:3 的比例在静态板中共培养或在 10%的过度循环拉伸应变下培养,并将结果与单独培养两种细胞类型进行比较,无论是否有循环应变。结果表明,在所有培养条件下,工程化关节软骨中 75%的软骨细胞可以用干细胞替代,胶原含量增加,糖胺聚糖含量超过拉伸培养的软骨细胞。在不观察到细胞活力的不良影响的情况下,可以做到这一点。与单独培养的软骨细胞在 10%应变下相比,当软骨细胞与干细胞以 1:3 的比例共培养时,胶原和糖胺聚糖的分泌分别增强了 6.1 倍和 2 倍。