Faculty of Agriculture, Veterinary Teaching Hospital, Tokyo University of Agriculture and Technology, Tokyo 183-8509, Japan.
Department of Surgery, Anesthesiology, and Radiology, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44519, Egypt.
Int J Mol Sci. 2024 Sep 13;25(18):9908. doi: 10.3390/ijms25189908.
Cryopreservation is essential for the broad clinical application of mesenchymal stem cells (MSCs), yet its impact on their cellular characteristics and cardiomyogenic differentiation potential remains a critical concern in translational medicine. This study aimed to evaluate the effects of cryopreservation on the biological properties and cardiomyogenic capacity of rat adipose-derived MSCs (AD-MSCs). We examined their cellular morphology, surface marker expression (CD29, CD90, CD45), trilineage differentiation potential (adipogenic, osteogenic, chondrogenic), and gene expression profiles for the pluripotency marker and immunomodulatory markers and . After inducing cardiomyocyte differentiation, we assessed cardiac-specific gene expressions (, , ) using quantitative RT-qPCR, along with live/dead cell staining and immunofluorescence for cardiac-specific proteins (Troponin T, α-actinin, Myosin Heavy Chain). Cryopreserved AD-MSCs preserved their morphology, surface markers, and differentiation potential, but exhibited a reduced expression of , , and . Additionally, cryopreservation diminished cardiomyogenic differentiation, as indicated by the lower levels of , , and seen compared to non-cryopreserved cells. Despite this, high cell viability (>90%) and maintained cardiac protein expression were observed post-cryopreservation. These findings highlight the necessity of optimizing cryopreservation protocols to ensure the full therapeutic potential of AD-MSCs, particularly in applications related to cardiac regenerative medicine.
冷冻保存对于间充质干细胞(MSCs)的广泛临床应用至关重要,但在转化医学中,其对细胞特性和心肌生成分化潜力的影响仍然是一个关键问题。本研究旨在评估冷冻保存对大鼠脂肪来源间充质干细胞(AD-MSCs)的生物学特性和心肌生成能力的影响。我们观察了它们的细胞形态、表面标志物表达(CD29、CD90、CD45)、三系分化潜能(成脂、成骨、软骨)以及多能性标志物和免疫调节标志物的基因表达谱。在诱导心肌细胞分化后,我们使用定量 RT-qPCR 评估了心脏特异性基因表达(、、),同时进行了活/死细胞染色和心脏特异性蛋白(肌钙蛋白 T、α-肌动蛋白、肌球蛋白重链)的免疫荧光染色。冷冻保存的 AD-MSCs 保持了其形态、表面标志物和分化潜能,但 、和的表达降低。此外,与未冷冻保存的细胞相比,冷冻保存降低了心肌生成分化,表现为 、和的水平降低。尽管如此,冷冻保存后仍观察到高细胞活力(>90%)和心脏蛋白表达的维持。这些发现强调了优化冷冻保存方案的必要性,以确保 AD-MSCs 的全部治疗潜力,特别是在与心脏再生医学相关的应用中。