|
Resolution: standard / high Figure 6.
Stem cells, administered intravenously, home to an inflammatory lesion in the brain. (a) An LPS lesion was induced on the right corpus callosum, followed by intravenous administration
of 50,000 IO-TAT-FITC-labelled eNCSCs (top row) or BMSCs (bottom row). Both cell types
migrated to the LPS-lesion site (arrows) from the peripheral vasculature within 24
hours of administration. False-colored inserts show better the hypointense regions.
(b) Both cells types migrated to the LPS lesion after intravenous injection. The IO-TAT-FITC
signal demonstrated that the cells had migrated to the lesioned brain area from the
peripheral vasculature 24 hours after injection (arrows; first column). Some FITC
signal was detected in IB4+ resident macrophages/microglia (arrows; second column; red). Similarly, limited differentiation
into GFAP+ glia was seen (arrows; third column; red). Scale bars: 1 mm (b; IO-TAT-FITC), 20 μm
(b; IB4, GFAP).
Jackson et al. Stem Cell Research & Therapy 2010 1:17 doi:10.1186/scrt17 |