Calcium
Background: Effective digestive enzymes are crucial for successful islet isolation. Supplemental proteases are essential because they synergize with collagenase for effective pancreatic digestion. The activity of these enzymes is critically dependent on the presence of Ca 2+ ions at a concentration...
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2018-07-01
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Series: | Cell Transplantation |
Online Access: | https://doi.org/10.1177/0963689718779350 |
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doaj-eb09f05569404390aaa4ccb93f8149ae2020-11-25T03:27:19ZengSAGE PublishingCell Transplantation0963-68971555-38922018-07-012710.1177/0963689718779350CalciumTorsten Eich0Magnus Ståhle1Bengt Gustafsson2Rune Horneland3Marko Lempinen4Torbjörn Lundgren5Ehab Rafael6Gunnar Tufveson7Bengt von Zur-Mühlen8Johan Olerud9Hanne Scholz10Olle Korsgren11 Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden Department of Transplantation, Sahlgrenska University Hospital, Gothenburg, Sweden Department of Transplantation, Oslo University Hospital, Rikshospitalet, Oslo, Norway Department of Transplantation and Liver Surgery, Helsinki University Hospital, Helsinki, Finland Division of Transplantation Surgery, CLINTEC, Karolinska University Hospital, Stockholm, Sweden Transplantation Unit, Department of Surgery, Skåne University Hospital, Malmö, Sweden Department of Surgical Sciences, Division of Transplantation Surgery, Uppsala University Hospital, Uppsala, Sweden Department of Surgical Sciences, Division of Transplantation Surgery, Uppsala University Hospital, Uppsala, Sweden Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden Department of Transplantation, Oslo University Hospital, Rikshospitalet, Oslo, Norway Department of Biomedicine, University of Gothenburg, Gothenburg, SwedenBackground: Effective digestive enzymes are crucial for successful islet isolation. Supplemental proteases are essential because they synergize with collagenase for effective pancreatic digestion. The activity of these enzymes is critically dependent on the presence of Ca 2+ ions at a concentration of 5–10 mM. The present study aimed to determine the Ca 2+ concentration during human islet isolation and to ascertain whether the addition of supplementary Ca 2+ is required to maintain an optimal Ca 2+ concentration during the various phases of the islet isolation process. Methods: Human islets were isolated according to standard methods and isolation parameters. Islet quality control and the number of isolations fulfilling standard transplantation criteria were evaluated. Ca 2+ was determined by using standard clinical chemistry routines. Islet isolation was performed with or without addition of supplementary Ca 2+ to reach a Ca 2+ of 5 mM. Results: Ca 2+ concentration was markedly reduced in bicarbonate-based buffers, especially if additional bicarbonate was used to adjust the pH as recommended by the Clinical Islet Transplantation Consortium. A major reduction in Ca 2+ concentration was also observed during pancreatic enzyme perfusion, digestion, and harvest. Additional Ca 2+ supplementation of media used for dissolving the enzymes and during digestion, perfusion, and harvest was necessary in order to obtain the concentration recommended for optimal enzyme activity and efficient liberation of a large number of islets from the human pancreas. Conclusions: Ca 2+ is to a large extent consumed during clinical islet isolation, and in the absence of supplementation, the concentration fell below that recommended for optimal enzyme activity. Ca 2+ supplementation of the media used during human pancreas digestion is necessary to maintain the concentration recommended for optimal enzyme activity. Addition of Ca 2+ to the enzyme blend has been implemented in the standard isolation protocols in the Nordic Network for Clinical Islet Transplantation.https://doi.org/10.1177/0963689718779350 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Torsten Eich Magnus Ståhle Bengt Gustafsson Rune Horneland Marko Lempinen Torbjörn Lundgren Ehab Rafael Gunnar Tufveson Bengt von Zur-Mühlen Johan Olerud Hanne Scholz Olle Korsgren |
spellingShingle |
Torsten Eich Magnus Ståhle Bengt Gustafsson Rune Horneland Marko Lempinen Torbjörn Lundgren Ehab Rafael Gunnar Tufveson Bengt von Zur-Mühlen Johan Olerud Hanne Scholz Olle Korsgren Calcium Cell Transplantation |
author_facet |
Torsten Eich Magnus Ståhle Bengt Gustafsson Rune Horneland Marko Lempinen Torbjörn Lundgren Ehab Rafael Gunnar Tufveson Bengt von Zur-Mühlen Johan Olerud Hanne Scholz Olle Korsgren |
author_sort |
Torsten Eich |
title |
Calcium |
title_short |
Calcium |
title_full |
Calcium |
title_fullStr |
Calcium |
title_full_unstemmed |
Calcium |
title_sort |
calcium |
publisher |
SAGE Publishing |
series |
Cell Transplantation |
issn |
0963-6897 1555-3892 |
publishDate |
2018-07-01 |
description |
Background: Effective digestive enzymes are crucial for successful islet isolation. Supplemental proteases are essential because they synergize with collagenase for effective pancreatic digestion. The activity of these enzymes is critically dependent on the presence of Ca 2+ ions at a concentration of 5–10 mM. The present study aimed to determine the Ca 2+ concentration during human islet isolation and to ascertain whether the addition of supplementary Ca 2+ is required to maintain an optimal Ca 2+ concentration during the various phases of the islet isolation process. Methods: Human islets were isolated according to standard methods and isolation parameters. Islet quality control and the number of isolations fulfilling standard transplantation criteria were evaluated. Ca 2+ was determined by using standard clinical chemistry routines. Islet isolation was performed with or without addition of supplementary Ca 2+ to reach a Ca 2+ of 5 mM. Results: Ca 2+ concentration was markedly reduced in bicarbonate-based buffers, especially if additional bicarbonate was used to adjust the pH as recommended by the Clinical Islet Transplantation Consortium. A major reduction in Ca 2+ concentration was also observed during pancreatic enzyme perfusion, digestion, and harvest. Additional Ca 2+ supplementation of media used for dissolving the enzymes and during digestion, perfusion, and harvest was necessary in order to obtain the concentration recommended for optimal enzyme activity and efficient liberation of a large number of islets from the human pancreas. Conclusions: Ca 2+ is to a large extent consumed during clinical islet isolation, and in the absence of supplementation, the concentration fell below that recommended for optimal enzyme activity. Ca 2+ supplementation of the media used during human pancreas digestion is necessary to maintain the concentration recommended for optimal enzyme activity. Addition of Ca 2+ to the enzyme blend has been implemented in the standard isolation protocols in the Nordic Network for Clinical Islet Transplantation. |
url |
https://doi.org/10.1177/0963689718779350 |
work_keys_str_mv |
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1724588313277366272 |