Lisboa Mateus de Oliveira, Selenko Ana Helena, Hochuli Agner Henrique Dorigo, Senegaglia Alexandra Cristina, Fracaro Letícia, Brofman Paulo Roberto Slud
Core for Cell Technology, School of Medicine and Health Sciences - Pontifícia Universidade Católica do Paraná, Curitiba, Paraná 80215-901, Brazil; National Institute of Science and Technology for Regenerative Medicine, INCT-REGENERA, 21941-599, Brazil.
Core for Cell Technology, School of Medicine and Health Sciences - Pontifícia Universidade Católica do Paraná, Curitiba, Paraná 80215-901, Brazil; National Institute of Science and Technology for Regenerative Medicine, INCT-REGENERA, 21941-599, Brazil.
Tissue Cell. 2024 Dec;91:102571. doi: 10.1016/j.tice.2024.102571. Epub 2024 Sep 24.
Dental Stem Cells (DSCs) from discarded teeth are a non-invasive and ethically favorable source with the potential for neurogenesis due to their ectodermal origin. Stem cells from human exfoliated deciduous teeth (SHED) are particularly promising due to their high differentiation potential and relative immaturity compared to other Mesenchymal Stromal Cells (MSCs). Markers like CD56 and CD271 are critical in identifying MSC subpopulations for therapeutic applications because of their roles in neurodevelopment and maintaining stemness. This study investigates how fetal bovine serum (FBS) concentrations affect the expression of CD56 and CD271 in SHED, influencing their stemness and neuronal differentiation potential. SHEDs were isolated from various donors, cultured, and characterized for MSC traits using markers such as CD14, CD19, CD29, CD34, CD45, CD73, CD90, CD105, CD56, and CD271. Culturing SHED in different FBS conditions (standard 15 %, reduced 1 % and 5 %, and FBS-free) showed that lower FBS concentrations increase CD271 and CD56 expression while maintaining the standard MSC immunophenotype. Importantly, the enhanced expression of these markers can be induced even after SHEDs have been expanded in standard FBS concentrations. These findings suggest that FBS concentration can optimize SHED culture conditions, enhancing their suitability for regenerative medicine and tissue engineering applications.
来自废弃牙齿的牙干细胞(DSCs)是一种非侵入性且符合伦理的来源,由于其外胚层起源而具有神经发生的潜力。人脱落乳牙干细胞(SHED)特别有前景,因为与其他间充质基质细胞(MSC)相比,它们具有高分化潜能且相对不成熟。像CD56和CD271这样的标志物对于识别用于治疗应用的MSC亚群至关重要,因为它们在神经发育和维持干性中发挥作用。本研究调查胎牛血清(FBS)浓度如何影响SHED中CD56和CD271的表达,从而影响它们的干性和神经元分化潜能。从不同供体分离出SHED,进行培养,并使用CD14、CD19、CD29、CD34、CD45、CD73、CD90、CD105、CD56和CD271等标志物对其MSC特性进行表征。在不同FBS条件(标准的15%、降低的1%和5%以及无FBS)下培养SHED表明,较低的FBS浓度会增加CD271和CD56的表达,同时保持标准的MSC免疫表型。重要的是,即使SHED在标准FBS浓度下扩增后,这些标志物的表达增强也可被诱导。这些发现表明FBS浓度可以优化SHED的培养条件,提高它们在再生医学和组织工程应用中的适用性。