Molecular imaging of myogenic stem/progenitor cells with [18F]-FHBG PET/CT system in SCID mice model of post-infarction heart

Abstract Preclinical and clinical studies have shown that stem cells can promote the regeneration of damaged tissues, but therapeutic protocols need better quality control to confirm the location and number of transplanted cells. This study describes in vivo imaging while assessing reporter gene exp...

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Main Authors: Weronika Wargocka-Matuszewska, Katarzyna Fiedorowicz, Anna Rugowska, Karolina Bednarowicz, Agnieszka Zimna, Łukasz Cheda, Paulina Hamankiewicz, Krzysztof Kilian, Michał Fiedorowicz, Monika Drabik, Natalia Rozwadowska, Zbigniew Rogulski, Maciej Kurpisz
Format: Article
Language:English
Published: Nature Portfolio 2021-10-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-98861-5
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author Weronika Wargocka-Matuszewska
Katarzyna Fiedorowicz
Anna Rugowska
Karolina Bednarowicz
Agnieszka Zimna
Łukasz Cheda
Paulina Hamankiewicz
Krzysztof Kilian
Michał Fiedorowicz
Monika Drabik
Natalia Rozwadowska
Zbigniew Rogulski
Maciej Kurpisz
author_facet Weronika Wargocka-Matuszewska
Katarzyna Fiedorowicz
Anna Rugowska
Karolina Bednarowicz
Agnieszka Zimna
Łukasz Cheda
Paulina Hamankiewicz
Krzysztof Kilian
Michał Fiedorowicz
Monika Drabik
Natalia Rozwadowska
Zbigniew Rogulski
Maciej Kurpisz
author_sort Weronika Wargocka-Matuszewska
collection DOAJ
description Abstract Preclinical and clinical studies have shown that stem cells can promote the regeneration of damaged tissues, but therapeutic protocols need better quality control to confirm the location and number of transplanted cells. This study describes in vivo imaging while assessing reporter gene expression by its binding to a radiolabelled molecule to the respective receptor expressed in target cells. Five mice underwent human skeletal muscle-derived stem/progenitor cell (huSkMDS/PC EF1-HSV-TK) intracardial transplantation after induction of myocardial infarction (MI). The metabolic parameters of control and post-infarction stem progenitor cell-implanted mice were monitored using 2-deoxy-18F-fluorodeoxyglucose ([18F]-FDG) before and after double promotor/reporter probe imaging with 9-(4-18F-fluoro-3-[hydroxymethyl]butyl)guanine ([18F]-FHBG) using positron emission tomography (PET) combined with computed tomography (CT). Standardized uptake values (SUVs) were then calculated based on set regions of interest (ROIs). Experimental animals were euthanized after magnetic resonance imaging (MRI). Molecular [18F]-FHBG imaging of myogenic stem/progenitor cells in control and post-infarction mice confirmed the survival and proliferation of transplanted cells, as shown by an increased or stable signal from the PET apparatus throughout the 5 weeks of monitoring. huSkMDS/PC EF1-HSV-TK transplantation improved cardiac metabolic ([18F]-FDG with PET) and haemodynamic (MRI) parameters. In vivo PET/CT and MRI revealed that the precise use of a promotor/reporter probe incorporated into stem/progenitor cells may improve non-invasive monitoring of targeted cellular therapy in the cardiovascular system.
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spelling doaj.art-f33b98080133421aafe01e382c326a3b2022-12-21T20:34:21ZengNature PortfolioScientific Reports2045-23222021-10-0111111210.1038/s41598-021-98861-5Molecular imaging of myogenic stem/progenitor cells with [18F]-FHBG PET/CT system in SCID mice model of post-infarction heartWeronika Wargocka-Matuszewska0Katarzyna Fiedorowicz1Anna Rugowska2Karolina Bednarowicz3Agnieszka Zimna4Łukasz Cheda5Paulina Hamankiewicz6Krzysztof Kilian7Michał Fiedorowicz8Monika Drabik9Natalia Rozwadowska10Zbigniew Rogulski11Maciej Kurpisz12Faculty of Chemistry, Biological and Chemical Research Centre, University of WarsawInstitute of Human Genetics Polish Academy of ScienceInstitute of Human Biology and Evolution, Faculty of Biology Adam, Mickiewicz UniversityInstitute of Human Genetics Polish Academy of ScienceInstitute of Human Genetics Polish Academy of ScienceFaculty of Chemistry, Biological and Chemical Research Centre, University of WarsawFaculty of Chemistry, Biological and Chemical Research Centre, University of WarsawHeavy Ion Laboratory, University of WarsawMossakowski Medical Research Centre Polish Academy of ScienceMossakowski Medical Research Centre Polish Academy of ScienceInstitute of Human Genetics Polish Academy of ScienceFaculty of Chemistry, Biological and Chemical Research Centre, University of WarsawInstitute of Human Genetics Polish Academy of ScienceAbstract Preclinical and clinical studies have shown that stem cells can promote the regeneration of damaged tissues, but therapeutic protocols need better quality control to confirm the location and number of transplanted cells. This study describes in vivo imaging while assessing reporter gene expression by its binding to a radiolabelled molecule to the respective receptor expressed in target cells. Five mice underwent human skeletal muscle-derived stem/progenitor cell (huSkMDS/PC EF1-HSV-TK) intracardial transplantation after induction of myocardial infarction (MI). The metabolic parameters of control and post-infarction stem progenitor cell-implanted mice were monitored using 2-deoxy-18F-fluorodeoxyglucose ([18F]-FDG) before and after double promotor/reporter probe imaging with 9-(4-18F-fluoro-3-[hydroxymethyl]butyl)guanine ([18F]-FHBG) using positron emission tomography (PET) combined with computed tomography (CT). Standardized uptake values (SUVs) were then calculated based on set regions of interest (ROIs). Experimental animals were euthanized after magnetic resonance imaging (MRI). Molecular [18F]-FHBG imaging of myogenic stem/progenitor cells in control and post-infarction mice confirmed the survival and proliferation of transplanted cells, as shown by an increased or stable signal from the PET apparatus throughout the 5 weeks of monitoring. huSkMDS/PC EF1-HSV-TK transplantation improved cardiac metabolic ([18F]-FDG with PET) and haemodynamic (MRI) parameters. In vivo PET/CT and MRI revealed that the precise use of a promotor/reporter probe incorporated into stem/progenitor cells may improve non-invasive monitoring of targeted cellular therapy in the cardiovascular system.https://doi.org/10.1038/s41598-021-98861-5
spellingShingle Weronika Wargocka-Matuszewska
Katarzyna Fiedorowicz
Anna Rugowska
Karolina Bednarowicz
Agnieszka Zimna
Łukasz Cheda
Paulina Hamankiewicz
Krzysztof Kilian
Michał Fiedorowicz
Monika Drabik
Natalia Rozwadowska
Zbigniew Rogulski
Maciej Kurpisz
Molecular imaging of myogenic stem/progenitor cells with [18F]-FHBG PET/CT system in SCID mice model of post-infarction heart
Scientific Reports
title Molecular imaging of myogenic stem/progenitor cells with [18F]-FHBG PET/CT system in SCID mice model of post-infarction heart
title_full Molecular imaging of myogenic stem/progenitor cells with [18F]-FHBG PET/CT system in SCID mice model of post-infarction heart
title_fullStr Molecular imaging of myogenic stem/progenitor cells with [18F]-FHBG PET/CT system in SCID mice model of post-infarction heart
title_full_unstemmed Molecular imaging of myogenic stem/progenitor cells with [18F]-FHBG PET/CT system in SCID mice model of post-infarction heart
title_short Molecular imaging of myogenic stem/progenitor cells with [18F]-FHBG PET/CT system in SCID mice model of post-infarction heart
title_sort molecular imaging of myogenic stem progenitor cells with 18f fhbg pet ct system in scid mice model of post infarction heart
url https://doi.org/10.1038/s41598-021-98861-5
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