Abstract
We report a new platform technology for visualizing transgene expression in living subjects using magnetic resonance imaging (MRI). Using a vector, we introduced an MRI reporter, a metalloprotein from the ferritin family, into specific host tissues. The reporter is made superparamagnetic as the cell sequesters endogenous iron from the organism. In this new approach, the cells construct the MRI contrast agent in situ using genetic instructions introduced by the vector. No exogenous metal-complexed contrast agent is required, thereby simplifying intracellular delivery. We used a replication-defective adenovirus vector to deliver the ferritin transgenes. Following focal inoculation of the vector into the mouse brain, we monitored the reporter activity using in vivo time-lapse MRI. We observed robust contrast in virus-transduced neurons and glia for several weeks. This technology is adaptable to monitor transgene expression in vivo in many tissue types and has numerous biomedical applications, such as visualizing preclinical therapeutic gene delivery.
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References
Contag, C.H. & Bachmann, M.H. Advances in in vivo bioluminescence imaging of gene expression. Annu. Rev. Biomed. Eng. 4, 235–260 (2002).
Gambhir, S.S. et al. Imaging adenoviral-directed reporter gene expression in living animals with positron emission tomography. Proc. Natl. Acad. Sci. USA 96, 2333–2338 (1999).
Louie, A.Y. et al. In vivo visualization of gene expression using magnetic resonance imaging. Nat. Biotechnol. 18, 321–325 (2000).
Weissleder, R. et al. In vivo magnetic resonance imaging of transgene expression. Nat. Med. 6, 351–355 (2000).
Koretsky, A.P., Brosnan, M.J., Chen, L.H., Chen, J.D. & Vandyke, T. NMR detection of creatine-kinase expressed in liver of transgenic mice — determination of free ADP levels. Proc. Natl. Acad. Sci. USA 87, 3112–3116 (1990).
Walter, G., Barton, E.R. & Sweeney, H.L. Noninvasive measurement of gene expression in skeletal muscle. Proc. Natl. Acad. Sci. USA 97, 5151–5155 (2000).
Stolz, J.F., Chang, S.B.R. & Kirschvink, J.L. Magnetotactic bacteria and single-domain magnetite in hemipelagic sediments. Nature 321, 849–851 (1986).
Bulte, J.W. et al. Magnetoferritin: characterization of a novel superparamagnetic MR contrast agent. J. Magn. Reson. Imag. 4, 497–505 (1994).
Gottesfeld, Z. & Neeman, M. Ferritin effect on the transverse relaxation of water: NMR microscopy at 9.4 T. Magn. Reson. Med. 35, 514–520 (1996).
Vymazal, J., Zak, O., Bulte, J.W.M., Aisen, P. & Brooks, R.A. T1 and T2 of ferritin solutions: effect of loading factor. Magn. Reson. Med. 36, 61–65 (1996).
Vymazal, J., Brooks, R.A., Bulte, J.W.M., Gordon, D. & Aisen, P. Iron uptake by ferritin: NMR relaxometry studies at low iron loads. J. Inorg. Biochem. 71, 153–157 (1998).
Welch, S. Transferrin: The Iron Carrier (CRC Press, Boca Raton, Florida, 1992).
Vymazal, J. et al. The relation between brain iron and NMR relaxation times: an in vitro study. Magn. Reson. Med. 35, 56–61 (1996).
Dhenain, M., Michot, J.L., Volk, A., Picq, J.L. & Boller, F. T2-weighted MRI studies of mouse lemurs: a primate model of brain aging. Neurobiol. Aging 18, 517–521 (1997).
Okon, E. et al. Biodegradation of magnetite dextran nanoparticles in the rat — a histologic and biophysical study. Lab. Invest. 71, 895–903 (1994).
Yeh, T.C., Zhang, W.G., Ildstad, S.T. & Ho, C. Intracellular labeling of T-cells with superparamagnetic contrast agents. Magn. Reson. Med. 30, 617–625 (1993).
Ahrens, E.T., Feili-Hariri, M., Genove, G. & Morel, P.A. Receptor-mediated endocytosis of iron-oxide particles provides efficient labeling of dendritic cells for in vivo MR imaging. Magn. Reson. Med. 46, 1006–1013 (2003).
Kircher, M.F. et al. In vivo high resolution three-dimensional imaging of antigen-specific cytotoxic T-lymphocyte trafficking to tumors. Cancer Res. 63, 6838–6846 (2003).
Bulte, J.W.M., Arbab, A.S., Douglas, T. & Frank, J.A. Preparation of magnetically labeled cells for cell tracking by magnetic resonance imaging. Meth. Enzymol. 386, 275–299 (2004).
Epsztejn, S. et al. H-ferritin subunit overexpression in erythroid cells reduces the oxidative stress response and induces multidrug resistance properties. Blood 94, 3593–3603 (1999).
Corsi, B. et al. Transient overexpression of human H- and L-ferritin chains in COS cells. Biochem. J. 330, 315–320 (1998).
Cozzi, A. et al. Overexpression of wild type and mutated human ferritin H-chain in HeLa cells — in vivo role of ferritin ferroxidase activity. J. Biol. Chem. 275, 25122–25129 (2000).
Santambrogio, P. et al. Production and characterization of recombinant heteropolymers of human ferritin H-chain and L-chain. J. Biol. Chem. 268, 12744–12748 (1993).
Levi, S. et al. Evidence that H-chains and L-chains have cooperative roles in the iron-uptake mechanism of human ferritin. Biochem. J. 288, 591–596 (1992).
Klausner, R.D. et al. Receptor-mediated endocytosis of transferrin in K562 cells. J. Biol. Chem. 258, 4715–4724 (1983).
Acknowledgements
We thank C. Robison, J. Horner and K. Hitchens for their assistance. Also, we thank P. Arosio (University of Brescia, Italy) for the ferritin cDNA and P. Santambrogio (San Raffaele Scientific Institute, Milan, Italy) for the rH02 antibody. This work was funded by the Pittsburgh Life Sciences Greenhouse and the US National Institutes of Health (R01-EB003453, P41-EB001977 and P50-AR049617).
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Supplementary information
Supplementary Fig. 1
In vitro uptake kinetics of 59Fe-enriched human transferring in A549 cells. (PDF 91 kb)
Supplementary Fig. 2
TfR-1 levels in AdV-FT transduced and control A549 cells. (PDF 90 kb)
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Genove, G., DeMarco, U., Xu, H. et al. A new transgene reporter for in vivo magnetic resonance imaging. Nat Med 11, 450–454 (2005). https://doi.org/10.1038/nm1208
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DOI: https://doi.org/10.1038/nm1208
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