Lee Hyungbin, Bae Allen, Kim John, Kingsley Karl
Department of Advanced Education in Orthodontics, School of Medicine, University of Nevada-Las Vegas, Las Vegas, NV 89106, USA.
Department of Clinical Sciences, School of Dental Medicine, University of Nevada-Las Vegas, Las Vegas, NV 89106, USA.
J Funct Biomater. 2023 Feb 8;14(2):91. doi: 10.3390/jfb14020091.
Dental pulp stem cells (DPSCs) are mesenchymal stem cells (MSCs) with the potential to differentiate in a limited number of other tissue types. Some evidence has suggested the modulation of DPSC growth may be mediated, in part, by exogenous extracellular matrix (ECM) glycoproteins, including fibronectin (FN) and laminin-5 (LN5). Although preliminary research suggests that some ECM glycoproteins may work as functional biomaterials to modulate DPSC growth responses, the primary goal of this project is to determine the specific effects of FN and LN5 on DPSC growth and viability. Using an existing DPSC repository, n = 16 DPSC isolates were cultured and 96-well growth assays were performed, which revealed FN, LN5 and the combination of these were sufficient to induce statistically significant changes in growth among five (n = 5) DPSC isolates. In addition, the administration of FN (either alone or in combination) was sufficient to induce the expression of alkaline phosphatase (ALP) and dentin sialophosphoprotein (DSPP), while LN5 induced the expression of ALP only, suggesting differential responsiveness among DPSCs. Moreover, these responses appeared to correlate with the expression of MSC biomarkers NANOG, Oct4 and Sox2. These results add to the growing body of evidence suggesting that functional biomaterials, such as ECM glycoproteins FN and LN5, are sufficient to induce phenotypic and differentiation-specific effects in a specific subset of DPSC isolates. More research will be needed to determine which biomarkers or additional factors are necessary and sufficient to induce the differentiation and development of DPSCs and for biomedical applications.
牙髓干细胞(DPSCs)是间充质干细胞(MSCs),具有分化为有限数量其他组织类型的潜力。一些证据表明,DPSC生长的调节可能部分由外源性细胞外基质(ECM)糖蛋白介导,包括纤连蛋白(FN)和层粘连蛋白-5(LN5)。尽管初步研究表明,一些ECM糖蛋白可能作为功能性生物材料来调节DPSC的生长反应,但该项目的主要目标是确定FN和LN5对DPSC生长和活力的具体影响。利用现有的DPSC库,培养了n = 16个DPSC分离株,并进行了96孔生长试验,结果显示FN、LN5及其组合足以在五个(n = 5)DPSC分离株中诱导生长的统计学显著变化。此外,单独或联合使用FN足以诱导碱性磷酸酶(ALP)和牙本质涎磷蛋白(DSPP)的表达,而LN5仅诱导ALP的表达,表明DPSC之间存在不同的反应性。此外,这些反应似乎与MSC生物标志物NANOG、Oct4和Sox2的表达相关。这些结果进一步证明,功能性生物材料,如ECM糖蛋白FN和LN5,足以在特定的DPSC分离株亚群中诱导表型和分化特异性效应。需要更多的研究来确定哪些生物标志物或其他因素对于诱导DPSC的分化和发育以及生物医学应用是必要且充分的。