Thein vitro effects of a bimodal contrast agent on cellular functions and relaxometry
Autor: | Jack Price, Sarah C. Morgan, Michel Modo, Thomas J. Meade, Steve C.R. Williams, Cecilie Brekke, Andrew S. Lowe |
---|---|
Rok vydání: | 2007 |
Předmět: |
Cell type
Pathology medicine.medical_specialty Cell Survival Cellular differentiation Contrast Media Gadolinium Biology Cell Line Mice Cell Movement In vivo medicine Animals Radiology Nuclear Medicine and imaging Viability assay Spectroscopy Cell Proliferation Neurons Rhodamines Cell growth Stem Cells Cell Differentiation Dextrans Magnetic Resonance Imaging Neural stem cell Cell culture Biophysics Molecular Medicine Stem cell Reactive Oxygen Species |
Zdroj: | NMR in Biomedicine. 20:77-89 |
ISSN: | 1099-1492 0952-3480 |
Popis: | The in vivo monitoring of cell survival and migration will be essential to the translation of cell-based therapies from the laboratory to clinical studies. The pre-labeling of cells with magnetic resonance imaging (MRI) contrast agents renders them visible in vivo for serial cellular imaging. However, little is known about the impact of the presence of these metal particles inside transplanted cells. The use of the bimodal contrast agent GRID made it possible to demonstrate by means of fluorescent microscopy and inductively coupled plasma mass spectrometry (ICP-MS) that, after 16 h of incubation (without the use of a transfection agent), neural stem cells (NSCs) were saturated and no longer incorporated particles. With this maximal uptake, no significant effect on cell viability was observed. However, a significant decrease in proliferation was evident in cells that underwent 24 h of labeling. A significant increase in reactive oxygen species was observed for all GRID labeling, with a very significant increase with 24 h of labeling. GRID labeling did not affect cell motility in comparison with PKH26-labeled NSCs in a glioma-based migration assay and also allowed differentiation into all major cell types of the brain. GRID-labeled cells induced a signal change of 47% on T2 measurements and allows a detection of cell clusters of ∼220 cells/µl. Further in vivo testing will be required to ensure that cell labeling with gadolinium-based MRI contrast agents does not impair their ability to repair. Copyright © 2006 John Wiley & Sons, Ltd. |
Databáze: | OpenAIRE |
Externí odkaz: |