Thammasat University Research Unit in Dental and Bone Substitute Biomaterials, Faculty of Dentistry, Thammasat University, Pathumthani, Thailand.
Faculty of Dentistry, Thammasat University, Pathumthani, Thailand.
PeerJ. 2024 Aug 23;12:e17913. doi: 10.7717/peerj.17913. eCollection 2024.
Dental pulp stem cells (DPSCs) possess mesenchymal stem cell characteristics and have potential for cell-based therapy. Cell expansion is essential to achieve sufficient cell numbers. However, continuous cell replication causes cell aging , which usually accompanies and potentially affect DPSC characteristics and activities. Continuous passaging could alter susceptibility to external factors such as drug treatment. Therefore, this study sought to investigate potential outcome of passaging on DPSC morphology and activities in the absence or presence of external factor.
Human DPSCs were subcultured until reaching early passages (P5), extended passages (P10), and late passages (P15). Cells were evaluated and compared for cell and nuclear morphologies, cell adhesion, proliferative capacity, alkaline phosphatase (ALP) activity, and gene expressions in the absence or presence of external factor. Alendronate (ALN) drug treatment was used as an external factor.
Continuous passaging of DPSCs gradually lost their normal spindle shape and increased in cell and nuclear sizes. DPSCs were vulnerable to ALN. The size and shape were altered, leading to morphological abnormality and inhomogeneity. Long-term culture and ALN interfered with cell adhesion. DPSCs were able to proliferate irrespective of cell passages but the rate of cell proliferation in late passages was slower. ALN at moderate dose inhibited cell growth. ALN caused reduction of ALP activity in early passage. In contrast, extended passage responded differently to ALN by increasing ALP activity. Late passage showed higher collagen but lower osteocalcin gene expressions compared with early passage in the presence of ALN.
An increase in passage number played critical role in cell morphology and activities as well as responses to the addition of an external factor. The effects of cell passage should be considered when used in basic science research and clinical applications.
牙髓干细胞(DPSCs)具有间充质干细胞的特征,具有细胞治疗的潜力。细胞扩增对于获得足够的细胞数量至关重要。然而,细胞的连续复制会导致细胞衰老,这通常伴随着并可能影响 DPSC 的特征和活性。连续传代会改变细胞对药物等外部因素的敏感性。因此,本研究旨在探讨在不存在或存在外部因素的情况下,传代对 DPSC 形态和活性的潜在影响。
将人牙髓干细胞进行传代培养,直至达到早期传代(P5)、扩展传代(P10)和晚期传代(P15)。评估和比较细胞和核形态、细胞黏附、增殖能力、碱性磷酸酶(ALP)活性以及在不存在或存在外部因素时的基因表达。使用阿伦膦酸钠(ALN)药物治疗作为外部因素。
DPSCs 的连续传代逐渐失去正常的纺锤形,细胞和核的大小增加。DPSCs 对 ALN 敏感。大小和形状发生改变,导致形态异常和不均匀。长期培养和 ALN 干扰细胞黏附。DPSCs 能够增殖,与细胞传代无关,但晚期传代的细胞增殖速度较慢。中等剂量的 ALN 抑制细胞生长。早期传代的 ALP 活性降低。相反,延长传代对 ALN 的反应不同,增加了 ALP 活性。与早期传代相比,晚期传代在存在 ALN 的情况下,胶原蛋白增加,而骨钙素基因表达降低。
传代次数的增加对细胞形态和活性以及对外部因素的反应起着关键作用。在基础科学研究和临床应用中使用时,应考虑细胞传代的影响。