Voga Metka
Veterinary Faculty, University of Ljubljana, Gerbičeva 60, 1000 Ljubljana, Slovenia.
Bioengineering (Basel). 2024 May 20;11(5):513. doi: 10.3390/bioengineering11050513.
Ascorbic acid (AA) plays a crucial role in both the proliferation and chondrogenic differentiation potential of mesenchymal stem/medicinal signalling cells (MSCs); these are both key aspects of their general therapeutic use and their increasing use in veterinary medicine. Current immunomodulatory therapies require efficient expansion of MSCs in the laboratory, while emerging tissue regeneration strategies, such as cartilage or bone repair, aim to use differentiated MSCs and modulate the expression of chondrogenic and hypertrophic markers. Our aim was to investigate whether the addition of AA to the growth medium enhances the proliferation of canine adipose-derived MSCs (cAMSCs) grown on standard plastic surfaces and whether it affects chondrogenic differentiation potential on silk fibroin (SF) films. We assessed cell viability with trypan blue and proliferation potential by calculating population doubling. Chondrogenic induction on SF films was assessed by Alcian blue staining and gene expression analysis of chondrogenic and hypertrophic genes. The results showed that growth medium with AA significantly enhanced the proliferation of cAMSCs without affecting cell viability and modulated the expression of chondrogenic and hypertrophic genes of cAMSCs grown on SF films. Our results suggest that AA may be used in growth medium for expansion of cAMSCs and, at the same time, provide the basis for future studies to investigate the role of AA and SF in chondrogenic differentiation of MSCs.
抗坏血酸(AA)在间充质干/药用信号细胞(MSCs)的增殖和软骨形成分化潜能中起着关键作用;这些都是其在一般治疗用途以及在兽医学中日益广泛应用的关键方面。当前的免疫调节疗法需要在实验室中高效扩增MSCs,而新兴的组织再生策略,如软骨或骨修复,旨在使用分化的MSCs并调节软骨形成和肥大标记物的表达。我们的目的是研究在生长培养基中添加AA是否能增强在标准塑料表面生长的犬脂肪来源的MSCs(cAMSCs)的增殖,以及它是否会影响丝素蛋白(SF)膜上的软骨形成分化潜能。我们用台盼蓝评估细胞活力,并通过计算群体倍增来评估增殖潜能。通过阿尔新蓝染色以及软骨形成和肥大基因的基因表达分析来评估SF膜上的软骨形成诱导。结果表明,添加AA的生长培养基显著增强了cAMSCs的增殖,而不影响细胞活力,并调节了在SF膜上生长的cAMSCs的软骨形成和肥大基因的表达。我们的结果表明,AA可用于cAMSCs扩增的生长培养基中,同时为未来研究AA和SF在MSCs软骨形成分化中的作用提供基础。