Cellular magnetic resonance with iron oxide nanoparticles: long-term persistence of SPIO signal in the CNS after transplanted cell death

Author:

Cianciaruso Chiara12,Pagani Antonella1,Martelli Cristina34,Bacigaluppi Marco5,Leonardo Squadrito Mario67,Lo Dico Alessia34,De Palma Michele67,Furlan Roberto5,Lucignani Giovanni48,Falini Andrea12,Biffi Alessandra9,Ottobrini Luisa34,Salvatore Politi Letterio1

Affiliation:

1. Neuroradiology Department & Neuroradiology Research Group, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy

2. Vita-Salute San Raffaele University, 20132 Milan, Italy

3. Department of Pathophysiology & Transplantation, University of Milan, Italy

4. Centre of Molecular & Cellular Imaging – IMAGO, Milan, Italy

5. Neurology Department, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy

6. The Swiss Institute for Experimental Cancer Research, School of Life Sciences, Swiss Federal Institute of Technology Lausanne, 1015 Lausanne, Switzerland

7. Angiogenesis & Tumor Targeting Research Unit & San Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy

8. Department of Health Sciences, University of Milan, 20144 Milan, Italy

9. San Raffaele Telethon Institute for Gene Therapy, Division of Regenerative Medicine, Stem Cells & Gene Therapy, San Raffaele Scientific Institute, 20132 Milan, Italy

Abstract

Aim: To study the specificity of cellular MRI based on superparamagnetic iron oxide particles (SPIOs), especially within the CNS. Materials & methods: A microglial cell line was engineered for the expression of a suicide gene, the receptor of diphtheria toxin (DT), and two reporter genes, green fluorescent protein and luciferase, in order to induce, in a controlled manner, cell death and test it through bioluminescence. SPIO-labeled DT-sensitive and control DT-insensitive cells were transplanted into the brains of mice, which underwent serial MRI and bioluminescence studies before and up to 90 days after DT-induced cell death. Results: No variations in SPIO signal voids were detected along longitudinal monitoring in brain hemispheres transplanted with DT-sensitive cells. Ex vivo analyses showed persistence of iron nanoparticle deposits at transplantation sites. Conclusion: Due to the long-term persistence of signal after transplanted cell death, caution is advised when SPIOs are employed for cell tracking. Original submitted 27 January 2014; Revised submitted 18 April 2014

Publisher

Future Medicine Ltd

Subject

Development,General Materials Science,Biomedical Engineering,Medicine (miscellaneous),Bioengineering

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