Clinic for Orthopedics and Trauma Surgery, University Hospital Bonn, 53127 Bonn, Germany.
Department of Orthopaedics and Trauma Surgery, University Medical Center Mannheim of University Heidelberg, 68167 Mannheim, Germany.
Int J Mol Sci. 2020 Nov 5;21(21):8309. doi: 10.3390/ijms21218309.
Osteoporosis is a disease characterized by low bone mass and an increased risk of fractures. Although several cellular players leading to osteoporosis have been identified, the role of mesenchymal stromal cells (MSC) is still not fully elaborated. The aim of this study was, therefore, to isolate and characterize MSCs from vertebral body of healthy non-osteoporotic and osteoporotic patients, with a particular focus on their osteogenic differentiation potential. Isolated MSCs were characterized by their osteogenic, adipogenic, and chondrogenic differentiation, as well as surface marker expression, proliferation behavior, and immunomodulatory capacity. The mineralization process was confirmed using Alizarin Red S and alkaline phosphatase (ALP) stains and further evaluated by determining ALP activity, mineral deposition, and free phosphate ion release. MSCs from both healthy and osteoporotic patients showed common fibroblast-like morphology and similar proliferation behavior. They expressed the typical MSC surface markers and possessed immunomodulatory capacity. Both groups demonstrated solid trilineage differentiation potential; osteogenic differentiation was further confirmed by increased ALP activity, deposition of inorganic crystals, phosphate ion release, and expression of osteoblast marker genes. Overall, MSCs from osteoporotic and non-osteoporotic patients showed neither a difference in general MSC features nor in the detailed analysis regarding osteogenic differentiation. These data suggest that vertebral body MSCs from osteoporotic patients were not impaired; rather, they possessed full osteogenic potential compared to MSCs from non-osteoporotic patients.
骨质疏松症是一种以骨量低和骨折风险增加为特征的疾病。尽管已经确定了几种导致骨质疏松症的细胞因子,但间充质基质细胞(MSC)的作用仍未完全阐明。因此,本研究的目的是从健康非骨质疏松症和骨质疏松症患者的椎体中分离和鉴定 MSC,并特别关注它们的成骨分化潜能。分离的 MSC 通过其成骨、成脂和成软骨分化以及表面标志物表达、增殖行为和免疫调节能力进行鉴定。通过茜素红 S 和碱性磷酸酶(ALP)染色确认矿化过程,并通过测定 ALP 活性、矿物质沉积和游离磷酸盐离子释放进一步评估。来自健康和骨质疏松症患者的 MSC 均表现出典型的成纤维细胞样形态和相似的增殖行为。它们表达典型的 MSC 表面标志物,具有免疫调节能力。两组均表现出稳定的三系分化潜能;成骨分化进一步通过增加 ALP 活性、无机晶体沉积、磷酸盐离子释放和骨细胞标记基因的表达得到证实。总体而言,来自骨质疏松症和非骨质疏松症患者的 MSC 既没有在一般 MSC 特征上存在差异,也没有在成骨分化的详细分析中存在差异。这些数据表明,与非骨质疏松症患者的 MSC 相比,来自骨质疏松症患者的椎体 MSC 并未受损;相反,它们具有完整的成骨潜能。