| Literature DB >> 27004132 |
Nathanael Raschzok1, Ulf Teichgräber2, Nils Billecke1, Anja Zielinski1, Kirsten Steinz1, Nora N Kammer1, Mehmet H Morgul3, Sarah Schmeisser1, Michaela K Adonopoulou1, Lars Morawietz4, Bernhard Hiebl5, Ruth Schwartlander6, Wolfgang Rüdinger7, Bernd Hamm2, Peter Neuhaus1, Igor M Sauer1.
Abstract
Liver cell transplantation (LCT) is a promising treatment approach for certain liver diseases, but clinical implementation requires methods for noninvasive follow-up. Labeling with superparamagnetic iron oxide particles can enable the detection of cells with magnetic resonance imaging (MRI). We investigated the feasibility of monitoring transplanted liver cells by MRI in a preclinical swine model and used this approach to evaluate different routes for cell application. Liver cells were isolated from landrace piglets and labeled with micron-sized iron oxide particles (MPIO) in adhesion. Labeled cells (n = 10), native cells (n = 3), or pure particles (n = 4) were transplanted to minipigs via intraportal infusion into the liver, direct injection into the splenic parenchyma, or intra-arterial infusion to the spleen. Recipients were investigated by repeated 3.0 Tesla MRI and computed tomography angiography up to 8 weeks after transplantation. Labeling with MPIO, which are known to have a strong effect on the magnetic field, enabled noninvasive detection of cell aggregates by MRI. Following intraportal application, which is commonly applied for clinical LCT, MRI was able to visualize the microembolization of transplanted cells in the liver that were not detected by conventional imaging modalities. Cells directly injected into the spleen were retained, whereas cell infusions intra-arterially into the spleen led to translocation and engraftment of transplanted cells in the liver, with significantly fewer microembolisms compared to intraportal application. These findings demonstrate that MRI can be a valuable tool for noninvasive elucidation of cellular processes of LCT and-if clinically applicable MPIO are available-for monitoring of LCT under clinical conditions. Moreover, the results clarify mechanisms relevant for clinical practice of LCT, suggesting that the intra-arterial route to the spleen deserves further evaluation.Entities:
Keywords: Cell tracking; Iron oxide particle; Liver cell transplantation (LCT); Magnetic resonance imaging (MRI); Micron-sized iron oxide particles (MPIO)
Year: 2010 PMID: 27004132 PMCID: PMC4789318 DOI: 10.3727/215517910X551053
Source DB: PubMed Journal: Cell Med ISSN: 2155-1790