Anna Naumova1,2,
Vasily Yarnykh1,2, Hans Reinecke2,3, Charles Murry2,3,
Chun Yuan1,2
1Radiology,
University of Washington, Seattle, WA, USA; 2Center for
Cardiovascular Biology, University of Washington, Seattle, WA, USA; 3Pathology,
University of Washington, Seattle, WA, USA
This study showed possibility of non-invasive visualization and quantification of transgenic C2C12 grafts overexpressing MRI gene reporter ferritin in the infarcted mouse heart. T2*-weighted gradient echo sequence was most sensitive for imaging of ferritin-tagged grafts capturing about 30% change in MRI signal intensity. Unlabeled wild-type C2C12 cells transplanted to the mouse heart did not change MRI signal intensity in T2*-weighted images. The important advantage of this approach is that the gene reporter divides with each round of cell division retaining a desired MRI contrast over the entire volume of growing grafts.
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