Uzieliene Ilona, Bialaglovyte Paulina, Miksiunas Rokas, Lebedis Ignas, Pachaleva Jolita, Vaiciuleviciute Raminta, Ramanaviciene Almira, Kvederas Giedrius, Bernotiene Eiva
Department of Regenerative Medicine, State Research Institute Centre for Innovative Medicine, LT-08406 Vilnius, Lithuania.
Department of Immunology, State Research Institute Centre for Innovative Medicine, LT-08406 Vilnius, Lithuania.
Bioengineering (Basel). 2023 Aug 24;10(9):1001. doi: 10.3390/bioengineering10091001.
Articular cartilage is an avascular tissue with a limited capacity for self-regeneration, leading the tissue to osteoarthritis (OA). Mesenchymal stem cells (MSCs) are promising for cartilage tissue engineering, as they are capable of differentiating into chondrocyte-like cells and secreting a number of active molecules that are important for cartilage extracellular matrix (ECM) synthesis. The aim of this study was to evaluate the potential of easily accessible menstrual blood-derived MSC (MenSC) paracrine factors in stimulating bone marrow MSC (BMMSCs) chondrogenic differentiation and to investigate their role in protecting cartilage from degradation in vitro. MenSCs and BMMSCs chondrogenic differentiation was induced using four different growth factors: TGF-β3, activin A, BMP-2, and IGF-1. The chondrogenic differentiation of BMMSCs was stimulated in co-cultures with MenSCs and cartilage explants co-cultured with MenSCs for 21 days. The chondrogenic capacity of BMMSCs was analyzed by the secretion of four growth factors and cartilage oligomeric matrix protein, as well as the release and synthesis of cartilage ECM proteins, and chondrogenic gene expression in cartilage explants. Our results suggest that MenSCs stimulate chondrogenic response in BMMSCs by secreting activin A and TGF-β3 and may have protective effects on cartilage tissue ECM by decreasing the release of GAGs, most likely through the modulation of activin A related molecular pathway. In conclusion, paracrine factors secreted by MenSCs may turn out to be a promising therapeutical approach for cartilage tissue protection and repair.
关节软骨是一种无血管组织,自我再生能力有限,易导致骨关节炎(OA)。间充质干细胞(MSC)在软骨组织工程中具有广阔前景,因为它们能够分化为软骨样细胞,并分泌多种对软骨细胞外基质(ECM)合成至关重要的活性分子。本研究旨在评估易于获取的月经血来源的MSC(MenSC)旁分泌因子刺激骨髓MSC(BMMSC)软骨形成分化的潜力,并研究它们在体外保护软骨免受降解中的作用。使用四种不同的生长因子:转化生长因子-β3(TGF-β3)、激活素A、骨形态发生蛋白-2(BMP-2)和胰岛素样生长因子-1(IGF-1)诱导MenSC和BMMSC的软骨形成分化。将BMMSC与MenSC共培养,以及将软骨外植体与MenSC共培养21天,以刺激BMMSC的软骨形成分化。通过四种生长因子和软骨寡聚基质蛋白的分泌、软骨ECM蛋白的释放和合成以及软骨外植体中软骨形成基因的表达来分析BMMSC的软骨形成能力。我们的结果表明,MenSC通过分泌激活素A和TGF-β3刺激BMMSC的软骨形成反应,并且可能通过减少糖胺聚糖(GAG)的释放对软骨组织ECM具有保护作用,最有可能是通过调节激活素A相关分子途径。总之,MenSC分泌的旁分泌因子可能成为软骨组织保护和修复的一种有前景的治疗方法。