Abstract Archives of the RSNA, 2004


SST13-09

In Vivo MRI-based Tracking of Magnetically Labelled, Intravenously-Injected Adult Neural Stem Cells in Mice Affected by MOG35-55-induced Experimental Autoimmune Encephalomyelitis (EAE)

Scientific Papers

Presented on December 3, 2004
Presented as part of SST13: Neuroradiology/Head and Neck (White Matter Analysis and Abnormalities)

Participants

Letterio Salvatore Politi MD, Presenter: Nothing to Disclose
Stefano Pluchino PhD, Abstract Co-Author: Nothing to Disclose
Marco Bacigaluppi, Abstract Co-Author: Nothing to Disclose
Marcello Cadioli, Abstract Co-Author: Nothing to Disclose
Gianvito Martino, Abstract Co-Author: Nothing to Disclose
Giuseppe Scotti, Abstract Co-Author: Nothing to Disclose
Nicoletta Anzalone, Abstract Co-Author: Nothing to Disclose
Andrea Falini, Abstract Co-Author: Nothing to Disclose
et al, Abstract Co-Author: Nothing to Disclose

PURPOSE

we have recently shown that intravenously-injected adult undifferentiated mouse neural stem cells (aNSCs) promote multifocal remyelination and functional recovery in mice affected by a chronic form of experimental autoimmune encephalomyelitis (EAE). Here we evaluated the in vivo tracking of magnetically labelled aNSCs by serial MRI scans along the post-transplantation follow up.

METHOD AND MATERIALS

aNSCs were labelled with 0.1 mg/ml of iron by incubation with poli-L-lysine (PLL) and super paramagnetic iron oxide (SPIO) particles (Endorem, Guebert) for 72 hours. 12 C57BL/6 mice were immunized with MOG35-55 in Complete freund’s adjuvantand 6 of them – at the onset of clinical signs suggestive of CNS demyelination - underwent intravenous injection of 1000000 labelled aNSCs. Longitudinal MR scans (at day 0, 10, 15, 20, 25, and 30 from the immunization) were taken along the study using a commercially available human 3T scanner adapted with an animal-dedicated surface coil. Neurological evaluation was carried out during all this period. Neuropathological analysis (Prussian blue) of the CNS of transplanted EAE mice was also performed at sacrifice.

RESULTS

magnetically labelled aNSCs were identified in the transplanted mice as small hypointense spots within the white matter lesions as early as one day after the i.v. injection but progressively fade out at either 5 or 10 days post-transplantation. Neuropathology confirmed the presence of iron-labeled transplanted cells within areas of demyelination and axonal damage. All 6 EAE mice transplanted with labelled aNSCs showed an almost complete recovery from the disease, while untreated EAE mice showed disease progression and important disability.

CONCLUSIONS

early temporal and spatial migration of i.v. administered SPIO-labelled neural stem cells can be monitored by MRI. Magnetically labelled aNSCs may induce disease recovery in a chronic mouse model of multiple sclerosis. SPIOs tracers may represent an helpful tool for tracking transplanted neural stem cells in either pre-clinical or clinical studies in both animal models and humans.

Cite This Abstract

Politi, L, Pluchino, S, Bacigaluppi, M, Cadioli, M, Martino, G, Scotti, G, Anzalone, N, Falini, A, et al, , In Vivo MRI-based Tracking of Magnetically Labelled, Intravenously-Injected Adult Neural Stem Cells in Mice Affected by MOG35-55-induced Experimental Autoimmune Encephalomyelitis (EAE).  Radiological Society of North America 2004 Scientific Assembly and Annual Meeting, November 28 - December 3, 2004 ,Chicago IL. http://archive.rsna.org/2004/4409375.html