4.4 Article

A Trimodal Imaging Platform for Tracking Viable Transplanted Pancreatic Islets In Vivo: F-19 MR, Fluorescence, and Bioluminescence Imaging

Journal

MOLECULAR IMAGING AND BIOLOGY
Volume 21, Issue 3, Pages 454-464

Publisher

SPRINGER
DOI: 10.1007/s11307-018-1270-3

Keywords

F-19 magnetic resonance imaging; Optical imaging; Pancreatic islets; Transplantation; Nanoparticles

Funding

  1. Czech Science Foundation [P205-16-03156S]
  2. Ministry of Health of the Czech Republic (Institute for Clinical and Experimental Medicine - IKEM) [IN 00023001]
  3. European Research Council (ERC) Starting Grant (CoNQUeST Grant) [336454]
  4. European Research Council (ERC) [336454] Funding Source: European Research Council (ERC)

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PurposeCombining specific and quantitative F-19 magnetic resonance imaging (MRI) with sensitive and convenient optical imaging provides complementary information about the distribution and viability of transplanted pancreatic islet grafts. In this study, pancreatic islets (PIs) were labeled with positively charged multimodal nanoparticles based on poly(lactic-co-glycolic acid) (PLGA-NPs) with encapsulated perfluoro-15-crown-5-ether and the near-infrared fluorescent dye indocyanine green.ProceduresOne thousand and three thousand bioluminescent PIs were transplanted into subcutaneous artificial scaffolds, which served as an alternative transplant site. The grafts were monitored using in vivo F-19 MR, fluorescence, and bioluminescence imaging in healthy rats for 2weeks.ResultsTransplanted PIs were unambiguously localized in the scaffolds by F-19 MRI throughout the whole experiment. Fluorescence was detected in the first 4days after transplantation only. Importantly, in vivo bioluminescence correlated with the F-19 MRI signal.ConclusionsWe developed a trimodal imaging platform for in vivo examination of transplanted PIs. Fluorescence imaging revealed instability of the fluorescent dye and its limited applicability for longitudinal in vivo studies. A correlation between the bioluminescence signal and the F-19 MRI signal indicated the fast clearance of PLGA-NPs from the transplantation site after cell death, which addresses a major issue with intracellular imaging labels. Therefore, the proposed PLGA-NP platform is reliable for reflecting the status of transplanted PIs in vivo.

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