MagA is sufficient for producing magnetic nanoparticles in mammalian cells, making it an MRI reporter
MagA достаточно для получения магнитных наночастиц в клетках млекопитающих, что позволяет использовать его в качестве репортера для МРТ
2008-05-27
SCID: 54.1/4tmdx6as
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MRI reporter geneMagAmagnetic nanoparticlesmagnetosomestransverse relaxivity
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Abstract (AI)
Magnetic resonance imaging (MRI) is routinely used to obtain anatomical images that have greatly advanced biomedical research and clinical health care today, but the full potential of MRI in providing functional, physiological, and molecular information is only beginning to emerge. In this work, we sought to provide a gene expression marker for MRI based on bacterial magnetosomes, tiny magnets produced by naturally occurring magnetotactic bacteria. Specifically, magA, a gene in magnetotactic bacteria known to be involved with iron transport, is expressed in a commonly used human cell line, 293FT, resulting in the production of magnetic, iron-oxide nanoparticles by these cells and leading to increased transverse relaxivity. MRI shows that these particles can be formed in vivo utilizing endogenous iron and can be used to visualize cells positive for magA. These results demonstrate that magA alone is sufficient to produce magnetic nanoparticles and that it is an appropriate candidate for an MRI reporter gene.
Key Findings
1
Expression of the bacterial magA gene in human 293FT cells produces magnetic iron-oxide nanoparticles.
2
MagA alone is sufficient for magnetic nanoparticle production and is a suitable MRI reporter gene candidate.
3
MagA-driven nanoparticles increase transverse relaxivity, enabling MRI-based detection of expressing cells.
4
The nanoparticles form in vivo using endogenous iron, without requiring externally supplied iron.
Research Object
MagA-expressing mammalian cells producing magnetic iron-oxide nanoparticles
Research Subject
MagA-mediated nanoparticle formation and the resulting MRI reporter capability, including increased transverse relaxivity and visualization of expressing cells
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2008-05-27
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