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Cited 2 time in webofscience Cited 1 time in scopus
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Human Organic Anion Transporting Polypeptide 1B3 Applied as an MRI-Based Reporter Gene

Authors
Baek, SE[Baek, Song-Ee]Ul-Haq, A[Ul-Haq, Asad]Kim, DH[Kim, Dae Hee]Choi, HW[Choi, Hyoung Wook]Kim, MJ[Kim, Myeong-Jin]Choi, HJ[Choi, Hye Jin]Kim, H[Kim, Honsoul]
Issue Date
Jun-2020
Publisher
KOREAN RADIOLOGICAL SOC
Keywords
Reporter gene; MRI; Gadoxetic acid; Gene therapy; OATP1B3
Citation
KOREAN JOURNAL OF RADIOLOGY, v.21, no.6, pp.726 - 735
Indexed
SCIE
SCOPUS
KCI
Journal Title
KOREAN JOURNAL OF RADIOLOGY
Volume
21
Number
6
Start Page
726
End Page
735
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/4396
DOI
10.3348/kjr.2019.0903
ISSN
1229-6929
Abstract
Objective: Recent innovations in biology are boosting gene and cell therapy, but monitoring the response to these treatments is difficult. The purpose of this study was to find an MRI-reporter gene that can be used to monitor gene or cell therapy and that can be delivered without a viral vector, as viral vector delivery methods can result in long-term complications. Materials and Methods: CMV promoter human organic anion transporting polypeptide 1B3 (CMV-hOATP183) cDNA or CMV-blank DNA (control) was transfected into HEK293 cells using Lipofectamine. OATP1B3 expression was confirmed by western blotting and confocal microscopy. In vitro cell phantoms were made using transfected HEK293 cells cultured in various concentrations of gadoxetic acid for 24 hours, and images of the phantoms were made with a 9.4T micro-MRI. In vivo xenograft tumors were made by implanting HEK293 cells transfected with CMV-hOATP1B3 (n = 4) or CMV-blank (n = 4) in 8 week old male nude mice, and MRI was performed before and after intravenous injection of gadoxetic acid (1.2 mu L/g). Results: Western blot and confocal microscopy after immunotluorescence staining revealed that only CMV-hOA7P1B3-transfected HEK293 cells produced abundant OATP1B3, which Localized at the cell membrane. OATP1B3 expression levels remained high through the 25th subculture cycle, but decreased substantially by the 50th subculture cycle. MRI of cell phantoms showed that only the CMV-hOATP1B3-transfected cells produced a significant contrast enhancement effect. In vivo MRI of xenograft tumors revealed that only CMV-hOATP1B3-transfected HEK293 tumors demonstrated a T1 contrast effect, which lasted for at least 5 hours. Conclusion: The human endogenous OATP1B3 gene can be non-virally delivered into cells to induce transient OATP1B3 expression, Leading to gadoxetic acid-mediated enhancement on MRI. These results indicate that hOATP1B3 can serve as an MRI-reporter gene while minimizing the risk of long-term complications.
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