FOCAS Research Institute, Technological University Dublin, City Campus, Dublin 8, Ireland.
NICB (National Institute for Cellular Biotechnology) at Dublin City University, Dublin 9, Ireland.
Analyst. 2024 Jul 22;149(15):4041-4053. doi: 10.1039/d4an00315b.
Chondrogenesis is a complex cellular process that involves the transformation of mesenchymal stem cells (MSCs) into chondrocytes, the specialised cells that form cartilage. In recent years, three-dimensional (3D) culture systems have emerged as a promising approach to studying cell behaviour and development in a more physiologically relevant environment compared to traditional two-dimensional (2D) cell culture. The use of these systems provided insights into the molecular mechanisms that regulate chondrogenesis and has the potential to revolutionise the development of new therapies for cartilage repair and regeneration. This study demonstrates the successful application of Raman microspectroscopy (RMS) as a label-free, non-destructive, and sensitive method to monitor the chondrogenic differentiation of bone marrow-derived rat mesenchymal stem cells (rMSCs) in a collagen type I hydrogel, and explores the potential benefits of 3D hydrogels compared to conventional 2D cell culture environments. rMSCs were cultured on 3D substrates for 3 weeks and their differentiation was monitored by measuring the spectral signatures of their subcellular compartments. Additionally, the evolution of high-density micromass cultures was investigated to provide a comprehensive understanding of the process and complex interactions between cells and their surrounding extracellular matrix. For comparison, rMSCs were induced into chondrogenesis in identical medium conditions for 21 days in monolayer culture. Raman spectra showed that rMSCs cultured in a collagen type I hydrogel are able to undergo a distinct chondrogenic differentiation pathway at a significantly higher rate than the 2D culture cells. 3D cultures expressed stronger and more homogeneous chondrogenesis-associated peaks such as collagens, glycosaminoglycans (GAGs), and aggrecan while manifesting changes in proteins and lipidic content. These results suggest that 3D type I collagen hydrogel substrates are promising for chondrogenesis studies, and that RMS is a valuable tool for monitoring chondrogenesis in 3D environments.
软骨发生是一个复杂的细胞过程,涉及间充质干细胞(MSCs)向软骨细胞的转化,软骨细胞是形成软骨的特化细胞。近年来,与传统的二维(2D)细胞培养相比,三维(3D)培养系统已成为研究细胞行为和发育的有前途的方法,因为 3D 培养系统提供了对调节软骨发生的分子机制的深入了解,并有可能彻底改变软骨修复和再生的新疗法的发展。本研究成功地应用了拉曼微光谱(RMS)作为一种无标记、非破坏性和敏感的方法,来监测骨髓源性大鼠间充质干细胞(rMSCs)在 I 型胶原水凝胶中的软骨发生分化,并探索了 3D 水凝胶与传统 2D 细胞培养环境相比的潜在优势。rMSCs 在 3D 基质上培养 3 周,并通过测量其细胞亚区的光谱特征来监测其分化。此外,还研究了高密度微团培养物的演变,以提供对细胞及其周围细胞外基质之间的复杂相互作用的全面了解。为了进行比较,在相同的培养基条件下,将 rMSCs 在单层培养中诱导 21 天以进行软骨发生。拉曼光谱表明,在 I 型胶原水凝胶中培养的 rMSCs 能够以比 2D 培养细胞高得多的速率经历明显的软骨发生分化途径。3D 培养物表达了更强且更均匀的与软骨发生相关的峰,例如胶原蛋白、糖胺聚糖(GAGs)和聚集蛋白聚糖,同时表现出蛋白质和脂类含量的变化。这些结果表明,I 型胶原水凝胶 3D 基质非常适合软骨发生研究,并且 RMS 是监测 3D 环境中软骨发生的有价值的工具。