In vivo imaging system for explants analysis-A new approach for assessment of cell transplantation effects in large animal models.

Despite spectacular progress in cellular transplantology, there are still many concerns about the fate of transplanted cells. More preclinical studies are needed, especially on large animal models, to bridge the translational gap between basic research and the clinic. Herein, we propose a novel appr...

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Main Authors: Weronika Zarychta-Wiśniewska, Anna Burdzinska, Radosław Zagozdzon, Bartosz Dybowski, Marta Butrym, Zdzisław Gajewski, Leszek Paczek
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5607129?pdf=render
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spelling doaj-eea791675b9f4834991c45a211c6aef52020-11-24T21:34:27ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01129e018458810.1371/journal.pone.0184588In vivo imaging system for explants analysis-A new approach for assessment of cell transplantation effects in large animal models.Weronika Zarychta-WiśniewskaAnna BurdzinskaRadosław ZagozdzonBartosz DybowskiMarta ButrymZdzisław GajewskiLeszek PaczekDespite spectacular progress in cellular transplantology, there are still many concerns about the fate of transplanted cells. More preclinical studies are needed, especially on large animal models, to bridge the translational gap between basic research and the clinic. Herein, we propose a novel approach in analysis of cell transplantation effects in large animals explants using in vivo imaging system (IVIS®) or similar equipment.In the in vitro experiment cells labeled with fluorescent membrane dyes: DID (far red) or PKH26 (orange) were visualized with IVIS®. The correlation between the fluorescence signal and cell number with or without addition of minced muscle tissue was calculated. In the ex vivo study urethras obtained from goats after intraurethral cells (n = 9) or PBS (n = 4) injections were divided into 0.5 cm cross-slices and analyzed by using IVIS®. Automatic algorithm followed or not by manual setup was used to separate specific dye signal from tissue autofluorescence. The results were verified by systematic microscopic analysis of standard 10 μm specimens prepared from slices before and after immunohistochemical staining. Comparison of obtained data was performed using diagnostic test function.Fluorescence signal strength in IVIS® was directly proportional to the number of cells regardless of the dye used and detectable for minimum 0.25x106 of cells. DID-derived signal was much less affected by the background signal in comparison to PKH26 in in vitro test. Using the IVIS® to scan explants in defined arrangement resulted in precise localization of DID but not PKH26 positive spots. Microscopic analysis of histological specimens confirmed the specificity (89%) and sensitivity (80%) of IVIS® assessment relative to DID dye. The procedure enabled successful immunohistochemical staining of specimens derived from analyzed slices.The IVIS® system under appropriate conditions of visualization and analysis can be used as a method for ex vivo evaluation of cell transplantation effects. Presented protocol allows for evaluation of cell delivery precision rate, enables semi-quantitative assessment of signal, preselects material for further analysis without interfering with the tissue properties. Far red dyes are appropriate fluorophores to cell labeling for this application.http://europepmc.org/articles/PMC5607129?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Weronika Zarychta-Wiśniewska
Anna Burdzinska
Radosław Zagozdzon
Bartosz Dybowski
Marta Butrym
Zdzisław Gajewski
Leszek Paczek
spellingShingle Weronika Zarychta-Wiśniewska
Anna Burdzinska
Radosław Zagozdzon
Bartosz Dybowski
Marta Butrym
Zdzisław Gajewski
Leszek Paczek
In vivo imaging system for explants analysis-A new approach for assessment of cell transplantation effects in large animal models.
PLoS ONE
author_facet Weronika Zarychta-Wiśniewska
Anna Burdzinska
Radosław Zagozdzon
Bartosz Dybowski
Marta Butrym
Zdzisław Gajewski
Leszek Paczek
author_sort Weronika Zarychta-Wiśniewska
title In vivo imaging system for explants analysis-A new approach for assessment of cell transplantation effects in large animal models.
title_short In vivo imaging system for explants analysis-A new approach for assessment of cell transplantation effects in large animal models.
title_full In vivo imaging system for explants analysis-A new approach for assessment of cell transplantation effects in large animal models.
title_fullStr In vivo imaging system for explants analysis-A new approach for assessment of cell transplantation effects in large animal models.
title_full_unstemmed In vivo imaging system for explants analysis-A new approach for assessment of cell transplantation effects in large animal models.
title_sort in vivo imaging system for explants analysis-a new approach for assessment of cell transplantation effects in large animal models.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description Despite spectacular progress in cellular transplantology, there are still many concerns about the fate of transplanted cells. More preclinical studies are needed, especially on large animal models, to bridge the translational gap between basic research and the clinic. Herein, we propose a novel approach in analysis of cell transplantation effects in large animals explants using in vivo imaging system (IVIS®) or similar equipment.In the in vitro experiment cells labeled with fluorescent membrane dyes: DID (far red) or PKH26 (orange) were visualized with IVIS®. The correlation between the fluorescence signal and cell number with or without addition of minced muscle tissue was calculated. In the ex vivo study urethras obtained from goats after intraurethral cells (n = 9) or PBS (n = 4) injections were divided into 0.5 cm cross-slices and analyzed by using IVIS®. Automatic algorithm followed or not by manual setup was used to separate specific dye signal from tissue autofluorescence. The results were verified by systematic microscopic analysis of standard 10 μm specimens prepared from slices before and after immunohistochemical staining. Comparison of obtained data was performed using diagnostic test function.Fluorescence signal strength in IVIS® was directly proportional to the number of cells regardless of the dye used and detectable for minimum 0.25x106 of cells. DID-derived signal was much less affected by the background signal in comparison to PKH26 in in vitro test. Using the IVIS® to scan explants in defined arrangement resulted in precise localization of DID but not PKH26 positive spots. Microscopic analysis of histological specimens confirmed the specificity (89%) and sensitivity (80%) of IVIS® assessment relative to DID dye. The procedure enabled successful immunohistochemical staining of specimens derived from analyzed slices.The IVIS® system under appropriate conditions of visualization and analysis can be used as a method for ex vivo evaluation of cell transplantation effects. Presented protocol allows for evaluation of cell delivery precision rate, enables semi-quantitative assessment of signal, preselects material for further analysis without interfering with the tissue properties. Far red dyes are appropriate fluorophores to cell labeling for this application.
url http://europepmc.org/articles/PMC5607129?pdf=render
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