Talukdar Yahfi, Rashkow Jason, Lalwani Gaurav, Kanakia Shruti, Sitharaman Balaji
Department of Biomedical Engineering, Stony Brook University, Stony Brook, NY 11794-5281.
Biomaterials. 2014 Jun;35(18):4863-4877. doi: 10.1016/j.biomaterials.2014.02.054. Epub 2014 Mar 25.
We report the effects of two-dimensional graphene nanostructures; graphene nano-onions (GNOs), graphene oxide nanoribbons (GONRs), and graphene oxide nanoplatelets (GONPs) on viability, and differentiation of human mesenchymal stem cells (MSCs). Cytotoxicity of GNOs, GONRs, and GONPs dispersed in distearoyl-sn-glycero-3-phosphoethanolamine-N-[amino(polyethylene glycol)] (DSPE-PEG), on adipose derived mesenchymal stem cells (adMSCs), and bone marrow-derived mesenchymal stem cells (bmMSCs) was assessed by AlamarBlue and Calcein AM viability assays at concentrations ranging from 5 to 300 μg/ml for 24 or 72 h. Cytotoxicity of the 2D graphene nanostructures was found to be dose dependent, not time dependent, with concentrations less than 50 μg/ml showing no significant differences compared to untreated controls. Differentiation potential of adMSCs to adipocytes and osteoblasts, - characterized by Oil Red O staining and elution, alkaline phosphatase activity, calcium matrix deposition and Alizarin Red S staining - did not change significantly when treated with the three graphene nanoparticles at a low (10 μg/ml) and high (50 μg/ml) concentration for 24 h. Transmission electron microscopy (TEM) and confocal Raman spectroscopy indicated cellular uptake of only GNOs and GONPs. The results lay the foundation for the use of these nanoparticles at potentially safe doses as ex vivo labels for MSC-based imaging and therapy.
我们报告了二维石墨烯纳米结构,即石墨烯纳米洋葱(GNOs)、氧化石墨烯纳米带(GONRs)和氧化石墨烯纳米片(GONPs)对人间充质干细胞(MSCs)活力和分化的影响。通过AlamarBlue和Calcein AM活力测定法,评估了分散在二硬脂酰-sn-甘油-3-磷酸乙醇胺-N-[氨基(聚乙二醇)](DSPE-PEG)中的GNOs、GONRs和GONPs,在浓度范围为5至300μg/ml、处理时间为24或72小时时,对脂肪来源的间充质干细胞(adMSCs)和骨髓来源的间充质干细胞(bmMSCs)的细胞毒性。发现二维石墨烯纳米结构的细胞毒性呈剂量依赖性,而非时间依赖性,浓度低于50μg/ml时与未处理的对照组相比无显著差异。通过油红O染色和洗脱、碱性磷酸酶活性、钙基质沉积和茜素红S染色来表征,adMSCs向脂肪细胞和成骨细胞的分化潜能,在用三种石墨烯纳米颗粒以低浓度(10μg/ml)和高浓度(50μg/ml)处理24小时后,没有显著变化。透射电子显微镜(TEM)和共聚焦拉曼光谱表明,只有GNOs和GONPs被细胞摄取。这些结果为将这些纳米颗粒以潜在安全剂量用作基于MSC的成像和治疗的体外标记奠定了基础。