Jasenc Lara, Stražar Klemen, Mihelič Anže, Mihalič Rene, Trebše Rihard, Haring Gregor, Jeras Matjaž, Zupan Janja
Department of Clinical Biochemistry, Faculty of Pharmacy, University of Ljubljana, Askerceva 7, 1000 Ljubljana, Slovenia.
Department of Orthopaedic Surgery, University Medical Centre Ljubljana, Zaloska 9, 1000 Ljubljana, Slovenia.
Life (Basel). 2022 Jun 15;12(6):899. doi: 10.3390/life12060899.
Human skeletal stem cells (hSSCs) were recently identified as podoplanin (PDPN)/CD73/CD164-positive and CD146-negative cells that decline with age, and play a role in the pathogenesis of osteoarthritis (OA). The aim of this study was to identify the hSSC-like properties of bone-derived mesenchymal stem/stromal cells (MSCs) of patients with late and early OA. : First, we performed gene expression profiling for the hSSC markers in 32 patients with late and early OA, and donors without OA. Having identified the low expression of hSSC markers in late OA patients, we further performed trilineage differentiation and immunophenotyping for hSSC makers in the selected subsets from each donor group. : Our results show no differences in osteogenesis, chondrogenesis, and adipogenesis between the MSCs from the three groups. However, the immunophenotyping shows lower CD164 in MSCs from early OA patients in comparison with late and no OA subjects ( = 0.002 and = 0.017). : Our study shows that the in vitro hSSC-like properties of bone-derived MSCs are similar in patients with early and late OA, and in donors without OA. However, the lower percentage of CD164-positive MSCs in early OA patients indicates the potential of CD164 as a marker of the onset of OA.
人类骨骼干细胞(hSSCs)最近被鉴定为波形蛋白(PDPN)/CD73/CD164阳性且CD146阴性的细胞,其数量会随着年龄增长而减少,并在骨关节炎(OA)的发病机制中起作用。本研究的目的是确定晚期和早期OA患者骨源性间充质干细胞(MSCs)的类hSSC特性。首先,我们对32例晚期和早期OA患者以及无OA的捐赠者的hSSC标志物进行了基因表达谱分析。在确定晚期OA患者中hSSC标志物表达较低后,我们进一步对每个捐赠者组中选定亚组的hSSC标志物进行了三系分化和免疫表型分析。我们的结果显示,三组间MSCs的成骨、软骨形成和脂肪形成能力无差异。然而,免疫表型分析显示,与晚期和无OA受试者相比,早期OA患者的MSCs中CD164水平较低(P = 0.002和P = 0.017)。我们的研究表明,晚期和早期OA患者以及无OA捐赠者的骨源性MSCs的体外类hSSC特性相似。然而,早期OA患者中CD164阳性MSCs的比例较低,表明CD164作为OA发病标志物的潜力。