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Human precision-cut cystic duct and gallbladder slices: a novel method for studying cholangiopathies

BACKGROUND AND AIMS: Precision-cut tissue slices (PCTS) are widely used as an ex vivo culture tissue culture technique to study pathogeneses of diseases and drug activities in organs in vitro. A novel application of the PCTS model may be in the field of translational research into cholangiopathies s...

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Autores principales: Fridrichs, Jeske, Hamel, Bart, Kelder, Wendy, van den Hoed, Ewoud, van den Heuvel, Marius C., Hulscher, Jan B. F., Olinga, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387522/
https://www.ncbi.nlm.nih.gov/pubmed/37528870
http://dx.doi.org/10.3389/fped.2023.1058319
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author Fridrichs, Jeske
Hamel, Bart
Kelder, Wendy
van den Hoed, Ewoud
van den Heuvel, Marius C.
Hulscher, Jan B. F.
Olinga, Peter
author_facet Fridrichs, Jeske
Hamel, Bart
Kelder, Wendy
van den Hoed, Ewoud
van den Heuvel, Marius C.
Hulscher, Jan B. F.
Olinga, Peter
author_sort Fridrichs, Jeske
collection PubMed
description BACKGROUND AND AIMS: Precision-cut tissue slices (PCTS) are widely used as an ex vivo culture tissue culture technique to study pathogeneses of diseases and drug activities in organs in vitro. A novel application of the PCTS model may be in the field of translational research into cholangiopathies such as biliary atresia. Therefore, the aim of this study was to apply the precision-cut slice technique to human bile duct and gallbladder tissue. METHODS: Cystic duct and gallbladder tissue derived from patients undergoing a cholecystectomy were collected, preserved and used for preparation of precision-cut cystic duct slices (PCCDS) and precision-cut gallbladder slices (PCGS). The PCCDS and PCGS were prepared using a mechanical tissue slicer and subsequently incubated for 24 and 48 h respectively in William's Medium E (WME) culture medium. Viability was assessed based on ATP/protein content and tissue morphology [hematoxylin and eosin (H&E) staining]. RESULTS: It was shown that viability, assessed by the ATP/protein content and morphology, of the PCCDS (n = 8) and PCGS (n = 8) could be maintained over the 24 and 48 h incubation period respectively. ATP/protein content of the PCCDS increased significantly from 0.58 ± 0.13 pmol/µg at 0 h to 2.4 ± 0.29 pmol/µg after 24 h incubation (P = .0003). A similar significant increase from 0.94 ± 0.22 pmol/µg at 0 h to 3.7 ± 0.41 pmol/µg after 24 h (P = .0005) and 4.2 ± 0.47 pmol/µg after 48 h (P = .0002) was observed in the PCGS. Morphological assessment of the PCCDS and PCGS showed viable tissue at 0 h and after 24 and 48 h incubation respectively. CONCLUSION: This study is the first to report on the use of the PCTS model for human gallbladder and cystic duct tissue. PCCDS and PCGS remain viable for an incubation period of at least 24 h, which makes them suitable for research purposes in the field of cholangiopathies, including biliary atresia.
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spelling pubmed-103875222023-08-01 Human precision-cut cystic duct and gallbladder slices: a novel method for studying cholangiopathies Fridrichs, Jeske Hamel, Bart Kelder, Wendy van den Hoed, Ewoud van den Heuvel, Marius C. Hulscher, Jan B. F. Olinga, Peter Front Pediatr Pediatrics BACKGROUND AND AIMS: Precision-cut tissue slices (PCTS) are widely used as an ex vivo culture tissue culture technique to study pathogeneses of diseases and drug activities in organs in vitro. A novel application of the PCTS model may be in the field of translational research into cholangiopathies such as biliary atresia. Therefore, the aim of this study was to apply the precision-cut slice technique to human bile duct and gallbladder tissue. METHODS: Cystic duct and gallbladder tissue derived from patients undergoing a cholecystectomy were collected, preserved and used for preparation of precision-cut cystic duct slices (PCCDS) and precision-cut gallbladder slices (PCGS). The PCCDS and PCGS were prepared using a mechanical tissue slicer and subsequently incubated for 24 and 48 h respectively in William's Medium E (WME) culture medium. Viability was assessed based on ATP/protein content and tissue morphology [hematoxylin and eosin (H&E) staining]. RESULTS: It was shown that viability, assessed by the ATP/protein content and morphology, of the PCCDS (n = 8) and PCGS (n = 8) could be maintained over the 24 and 48 h incubation period respectively. ATP/protein content of the PCCDS increased significantly from 0.58 ± 0.13 pmol/µg at 0 h to 2.4 ± 0.29 pmol/µg after 24 h incubation (P = .0003). A similar significant increase from 0.94 ± 0.22 pmol/µg at 0 h to 3.7 ± 0.41 pmol/µg after 24 h (P = .0005) and 4.2 ± 0.47 pmol/µg after 48 h (P = .0002) was observed in the PCGS. Morphological assessment of the PCCDS and PCGS showed viable tissue at 0 h and after 24 and 48 h incubation respectively. CONCLUSION: This study is the first to report on the use of the PCTS model for human gallbladder and cystic duct tissue. PCCDS and PCGS remain viable for an incubation period of at least 24 h, which makes them suitable for research purposes in the field of cholangiopathies, including biliary atresia. Frontiers Media S.A. 2023-07-17 /pmc/articles/PMC10387522/ /pubmed/37528870 http://dx.doi.org/10.3389/fped.2023.1058319 Text en © 2023 Fridrichs, Hamel, Kelder, van den Hoed, van den Heuvel, Hulscher and Olinga. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Fridrichs, Jeske
Hamel, Bart
Kelder, Wendy
van den Hoed, Ewoud
van den Heuvel, Marius C.
Hulscher, Jan B. F.
Olinga, Peter
Human precision-cut cystic duct and gallbladder slices: a novel method for studying cholangiopathies
title Human precision-cut cystic duct and gallbladder slices: a novel method for studying cholangiopathies
title_full Human precision-cut cystic duct and gallbladder slices: a novel method for studying cholangiopathies
title_fullStr Human precision-cut cystic duct and gallbladder slices: a novel method for studying cholangiopathies
title_full_unstemmed Human precision-cut cystic duct and gallbladder slices: a novel method for studying cholangiopathies
title_short Human precision-cut cystic duct and gallbladder slices: a novel method for studying cholangiopathies
title_sort human precision-cut cystic duct and gallbladder slices: a novel method for studying cholangiopathies
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10387522/
https://www.ncbi.nlm.nih.gov/pubmed/37528870
http://dx.doi.org/10.3389/fped.2023.1058319
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