期刊
BIOMATERIALS
卷 35, 期 18, 页码 4863-4877出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2014.02.054
关键词
Graphene; Stem cells; Carbon nanoparticles; Differentiation
资金
- National Institutes of Health [1DP20D007394-01]
- U.S. Department of Energy, Office of Basic Energy Sciences [DE-ACO2-98CH10886]
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 GNO5, 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 mu g/m1 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 jig/m1 showing no significant differences compared to untreated controls. Differentiation potential of adMSCs to adipocytes and osteoblasts, characterized by Oil Red 0 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 mu g/ml) and high (50 mu g/m1) 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. (c) 2014 Elsevier Ltd. All rights reserved.
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