Functional Hepatocyte Culture and its Application to Cell Therapies
Since Berry and Friend developed methods to isolate hepatocytes from the liver by a collagenase digestion technique in 1969, studies in laboratory animals have demonstrated that hepatocyte transplantation could potentially be used for the treatment of liver failure and inborn errors of liver-based m...
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2006-11-01
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doaj-fb416784e96a4ae1b008fc415c4bc7832020-11-25T03:46:05ZengSAGE PublishingCell Transplantation0963-68971555-38922006-11-011510.3727/000000006783981332Functional Hepatocyte Culture and its Application to Cell TherapiesKimiaki Tanaka0Alejandro Soto-Gutierrez1Nalu Navarro-Alvarez2Jorge David Rivas-Carrillo3Hee-Sook Jun4Naoya Kobayashi M.D., Ph.D.5 Department of Surgery, Okayama University Graduate School of Medicine and Dentistry, Okayama 700-8558, Japan Department of Surgery, Okayama University Graduate School of Medicine and Dentistry, Okayama 700-8558, Japan Department of Surgery, Okayama University Graduate School of Medicine and Dentistry, Okayama 700-8558, Japan Department of Surgery, Okayama University Graduate School of Medicine and Dentistry, Okayama 700-8558, Japan Rosalind Franklin Comprehensive Diabetes Center, Chicago Medical School, North Chicago, IL 60064, USA Department of Surgery, Okayama University Graduate School of Medicine and Dentistry, Okayama 700-8558, JapanSince Berry and Friend developed methods to isolate hepatocytes from the liver by a collagenase digestion technique in 1969, studies in laboratory animals have demonstrated that hepatocyte transplantation could potentially be used for the treatment of liver failure and inborn errors of liver-based metabolism. Healthy human hepatocytes are an ideal source for hepatocyte transplantation; however, their relative scarcity is one of the major drawbacks, further compounded by the competing demands of liver transplantation. Notably, most of the hepatocytes are isolated from discarded livers that are not suitable for organ transplantation for a variety of reasons, including excessive fat content. Importantly, the hepatocyte isolation procedure itself exerts major stress on hepatocytes by the disruption of cell-to-cell and cell-to-matrix contacts, resulting in hepatocytic apoptosis. Prevention of apoptosis would maximize yield of healthy cells and maintain hepatocyte differentiated function in culture. In this review, we describe methods to prevent apoptosis by utilizing both antiapoptotic molecules and matrices. We also introduce a new type of liver tissue engineering, hepatocyte sheet transplantation, which utilizes unwoven cloth having a cellular adhesive property.https://doi.org/10.3727/000000006783981332 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kimiaki Tanaka Alejandro Soto-Gutierrez Nalu Navarro-Alvarez Jorge David Rivas-Carrillo Hee-Sook Jun Naoya Kobayashi M.D., Ph.D. |
spellingShingle |
Kimiaki Tanaka Alejandro Soto-Gutierrez Nalu Navarro-Alvarez Jorge David Rivas-Carrillo Hee-Sook Jun Naoya Kobayashi M.D., Ph.D. Functional Hepatocyte Culture and its Application to Cell Therapies Cell Transplantation |
author_facet |
Kimiaki Tanaka Alejandro Soto-Gutierrez Nalu Navarro-Alvarez Jorge David Rivas-Carrillo Hee-Sook Jun Naoya Kobayashi M.D., Ph.D. |
author_sort |
Kimiaki Tanaka |
title |
Functional Hepatocyte Culture and its Application to Cell Therapies |
title_short |
Functional Hepatocyte Culture and its Application to Cell Therapies |
title_full |
Functional Hepatocyte Culture and its Application to Cell Therapies |
title_fullStr |
Functional Hepatocyte Culture and its Application to Cell Therapies |
title_full_unstemmed |
Functional Hepatocyte Culture and its Application to Cell Therapies |
title_sort |
functional hepatocyte culture and its application to cell therapies |
publisher |
SAGE Publishing |
series |
Cell Transplantation |
issn |
0963-6897 1555-3892 |
publishDate |
2006-11-01 |
description |
Since Berry and Friend developed methods to isolate hepatocytes from the liver by a collagenase digestion technique in 1969, studies in laboratory animals have demonstrated that hepatocyte transplantation could potentially be used for the treatment of liver failure and inborn errors of liver-based metabolism. Healthy human hepatocytes are an ideal source for hepatocyte transplantation; however, their relative scarcity is one of the major drawbacks, further compounded by the competing demands of liver transplantation. Notably, most of the hepatocytes are isolated from discarded livers that are not suitable for organ transplantation for a variety of reasons, including excessive fat content. Importantly, the hepatocyte isolation procedure itself exerts major stress on hepatocytes by the disruption of cell-to-cell and cell-to-matrix contacts, resulting in hepatocytic apoptosis. Prevention of apoptosis would maximize yield of healthy cells and maintain hepatocyte differentiated function in culture. In this review, we describe methods to prevent apoptosis by utilizing both antiapoptotic molecules and matrices. We also introduce a new type of liver tissue engineering, hepatocyte sheet transplantation, which utilizes unwoven cloth having a cellular adhesive property. |
url |
https://doi.org/10.3727/000000006783981332 |
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