TY - JOUR
T1 - Multimodal imaging of micron-sized iron oxide particles following in vitro and in vivo uptake by stem cells
T2 - Down to the nanometer scale
AU - Roose, Dimitri
AU - Leroux, Frederic
AU - De Vocht, Nathalie
AU - Guglielmetti, Caroline
AU - Pintelon, Isabel
AU - Adriaensen, Dirk
AU - Ponsaerts, Peter
AU - Van der Linden, Annemie
AU - Bals, Sara
N1 - Publisher Copyright:
© 2014 John Wiley & Sons, Ltd.
PY - 2014/11/1
Y1 - 2014/11/1
N2 - In this study, the interaction between cells and micron-sized paramagnetic iron oxide (MPIO) particles was investigated by characterizing MPIO in their original state, and after cellular uptake in vitro as well as in vivo. Moreover, MPIO in the olfactory bulb were studied 9months after injection. Using various imaging techniques, cell-MPIO interactions were investigated with increasing spatial resolution. Live cell confocal microscopy demonstrated that MPIO co-localize with lysosomes after in vitro cellular uptake. In more detail, a membrane surrounding the MPIO was observed by high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM). Following MPIO uptake in vivo, the same cell-MPIO interaction was observed by HAADF-STEM in the subventricular zone at 1week and in the olfactory bulb at 9months after MPIO injection. These findings provide proof for the current hypothesis that MPIO are internalized by the cell through endocytosis. The results also show MPIO are not biodegradable, even after 9months in the brain. Moreover, they show the possibility of HAADF-STEM generating information on the labeled cell as well as on the MPIO. In summary, the methodology presented here provides a systematic route to investigate the interaction between cells and nanoparticles from the micrometer level down to the nanometer level and beyond.
AB - In this study, the interaction between cells and micron-sized paramagnetic iron oxide (MPIO) particles was investigated by characterizing MPIO in their original state, and after cellular uptake in vitro as well as in vivo. Moreover, MPIO in the olfactory bulb were studied 9months after injection. Using various imaging techniques, cell-MPIO interactions were investigated with increasing spatial resolution. Live cell confocal microscopy demonstrated that MPIO co-localize with lysosomes after in vitro cellular uptake. In more detail, a membrane surrounding the MPIO was observed by high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM). Following MPIO uptake in vivo, the same cell-MPIO interaction was observed by HAADF-STEM in the subventricular zone at 1week and in the olfactory bulb at 9months after MPIO injection. These findings provide proof for the current hypothesis that MPIO are internalized by the cell through endocytosis. The results also show MPIO are not biodegradable, even after 9months in the brain. Moreover, they show the possibility of HAADF-STEM generating information on the labeled cell as well as on the MPIO. In summary, the methodology presented here provides a systematic route to investigate the interaction between cells and nanoparticles from the micrometer level down to the nanometer level and beyond.
KW - Cell tracking
KW - HAADF-STEM
KW - MPIO
KW - TEM
KW - in vivo
UR - http://www.scopus.com/inward/record.url?scp=84915809513&partnerID=8YFLogxK
U2 - 10.1002/cmmi.1594
DO - 10.1002/cmmi.1594
M3 - Article
C2 - 24753446
AN - SCOPUS:84915809513
SN - 1555-4309
VL - 9
SP - 400
EP - 408
JO - Contrast Media and Molecular Imaging
JF - Contrast Media and Molecular Imaging
IS - 6
ER -