Nano-engineered skin mesenchymal stem cells: potential vehicles for tumour-targeted quantum-dot delivery

• Published in: Beilstein journal of nanotechnology Vol. 8; no. 1; pp. 1218 - 1230
• Main Authors: Saulite, Liga, Dapkute, Dominyka, Pleiko, Karlis, Popena, Ineta, Steponkiene, Simona, Rotomskis, Ricardas, Riekstina, Una
• Format: Journal Article
• Language: English
• Published: Germany Beilstein-Institut zur Föerderung der Chemischen Wissenschaften 2017; Beilstein-Institut
• Subjects: Biomarkers; Biomedical materials; Bone marrow; Cell cycle; Cell division; Cytoplasm; Diagnostic systems; Drug delivery systems; endocytosis; Endosomes; Experiments; Flow cytometry; Fluorescence; Full Research Paper; Labeling; Lipids; Lysosomes; mesenchymal stem cells; Nanoparticles; Nanoscience; Nanotechnology; Quantum dots; Skin cancer; stem cell differentiation; Stem cells; Tumors; quantum dots; endocytosis; stem cell differentiation; mesenchymal stem cells
• ISSN: 2190-4286; 2190-4286
• DOI: 10.3762/bjnano.8.123

Nanotechnology-based drug design offers new possibilities for the use of nanoparticles in imaging and targeted therapy of tumours. Due to their tumour-homing ability, nano-engineered mesenchymal stem cells (MSCs) could be utilized as vectors to deliver diagnostic and therapeutic nanoparticles into a tumour. In the present study, uptake and functional effects of carboxyl-coated quantum dots QD655 were studied in human skin MSCs. The effect of QD on MSCs was examined using a cell viability assay, Ki67 expression analysis, and tri-lineage differentiation assay. The optimal conditions for QD uptake in MSCs were determined using flow cytometry. The QD uptake route in MSCs was examined via fluorescence imaging using endocytosis inhibitors for the micropinocytosis, phagocytosis, lipid-raft, clathrin- and caveolin-dependent endocytosis pathways. These data showed that QDs were efficiently accumulated in the cytoplasm of MSCs after incubation for 6 h. The main uptake route of QDs in skin MSCs was clathrin-mediated endocytosis. QDs were mainly localized in early endosomes after 6 h as well as in late endosomes and lysosomes after 24 h. QDs in concentrations ranging from 0.5 to 64 nM had no effect on cell viability and proliferation. The expression of MSC markers, CD73 and CD90, and hematopoietic markers, CD34 and CD45, as well as the ability to differentiate into adipocytes, chondrocytes, and osteocytes, were not altered in the presence of QDs. We observed a decrease in the QD signal from labelled MSCs over time that could partly reflect QD excretion. Altogether, these data suggest that QD-labelled MSCs could be used for targeted drug delivery studies.