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Experimental Applications of in situ Liver Perfusion Machinery for the Study of Liver Disease
The liver is involved in a wide range of activities in vertebrates and some other animals, including metabolism, protein synthesis, detoxification, and the immune system. Until now, various methods have been devised to study liver diseases; however, each method has its own limitations. In situ liver...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Molecular and Cellular Biology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354060/ https://www.ncbi.nlm.nih.gov/pubmed/30665288 http://dx.doi.org/10.14348/molcells.2018.0330 |
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author | Choi, Won-Mook Eun, Hyuk Soo Lee, Young-Sun Kim, Sun Jun Kim, Myung-Ho Lee, Jun-Hee Shim, Young-Ri Kim, Hee-Hoon Kim, Ye Eun Yi, Hyon-Seung Jeong, Won-Il |
author_facet | Choi, Won-Mook Eun, Hyuk Soo Lee, Young-Sun Kim, Sun Jun Kim, Myung-Ho Lee, Jun-Hee Shim, Young-Ri Kim, Hee-Hoon Kim, Ye Eun Yi, Hyon-Seung Jeong, Won-Il |
author_sort | Choi, Won-Mook |
collection | PubMed |
description | The liver is involved in a wide range of activities in vertebrates and some other animals, including metabolism, protein synthesis, detoxification, and the immune system. Until now, various methods have been devised to study liver diseases; however, each method has its own limitations. In situ liver perfusion machinery, originally developed in rats, has been successfully adapted to mice, enabling the study of liver diseases. Here we describe the protocol, which is a simple but widely applicable method for investigating the liver diseases. The liver is perfused in situ by cannulation of the portal vein and suprahepatic inferior vena cava (IVC), with antegrade closed circuit circulation completed by clamping the infrahepatic IVC. In situ liver perfusion can be utilized to evaluate immune cell migration and function, hemodynamics and related cellular reactions in each type of hepatic cells, and the metabolism of toxic or other compounds by changing the composition of the circulating media. In situ liver perfusion method maintains liver function and cell viability for up to 2 h. This study also describes an optional protocol using density-gradient centrifugation for the separation of different types of hepatic cells, allowing the determination of changes in each cell type. In summary, this method of in situ liver perfusion will be useful for studying liver diseases as a complement to other established methods. |
format | Online Article Text |
id | pubmed-6354060 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Korean Society for Molecular and Cellular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-63540602019-02-11 Experimental Applications of in situ Liver Perfusion Machinery for the Study of Liver Disease Choi, Won-Mook Eun, Hyuk Soo Lee, Young-Sun Kim, Sun Jun Kim, Myung-Ho Lee, Jun-Hee Shim, Young-Ri Kim, Hee-Hoon Kim, Ye Eun Yi, Hyon-Seung Jeong, Won-Il Mol Cells Article The liver is involved in a wide range of activities in vertebrates and some other animals, including metabolism, protein synthesis, detoxification, and the immune system. Until now, various methods have been devised to study liver diseases; however, each method has its own limitations. In situ liver perfusion machinery, originally developed in rats, has been successfully adapted to mice, enabling the study of liver diseases. Here we describe the protocol, which is a simple but widely applicable method for investigating the liver diseases. The liver is perfused in situ by cannulation of the portal vein and suprahepatic inferior vena cava (IVC), with antegrade closed circuit circulation completed by clamping the infrahepatic IVC. In situ liver perfusion can be utilized to evaluate immune cell migration and function, hemodynamics and related cellular reactions in each type of hepatic cells, and the metabolism of toxic or other compounds by changing the composition of the circulating media. In situ liver perfusion method maintains liver function and cell viability for up to 2 h. This study also describes an optional protocol using density-gradient centrifugation for the separation of different types of hepatic cells, allowing the determination of changes in each cell type. In summary, this method of in situ liver perfusion will be useful for studying liver diseases as a complement to other established methods. Korean Society for Molecular and Cellular Biology 2019-01-31 2018-12-12 /pmc/articles/PMC6354060/ /pubmed/30665288 http://dx.doi.org/10.14348/molcells.2018.0330 Text en © The Korean Society for Molecular and Cellular Biology. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/. |
spellingShingle | Article Choi, Won-Mook Eun, Hyuk Soo Lee, Young-Sun Kim, Sun Jun Kim, Myung-Ho Lee, Jun-Hee Shim, Young-Ri Kim, Hee-Hoon Kim, Ye Eun Yi, Hyon-Seung Jeong, Won-Il Experimental Applications of in situ Liver Perfusion Machinery for the Study of Liver Disease |
title | Experimental Applications of in situ Liver Perfusion Machinery for the Study of Liver Disease |
title_full | Experimental Applications of in situ Liver Perfusion Machinery for the Study of Liver Disease |
title_fullStr | Experimental Applications of in situ Liver Perfusion Machinery for the Study of Liver Disease |
title_full_unstemmed | Experimental Applications of in situ Liver Perfusion Machinery for the Study of Liver Disease |
title_short | Experimental Applications of in situ Liver Perfusion Machinery for the Study of Liver Disease |
title_sort | experimental applications of in situ liver perfusion machinery for the study of liver disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354060/ https://www.ncbi.nlm.nih.gov/pubmed/30665288 http://dx.doi.org/10.14348/molcells.2018.0330 |
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