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Calcium: A Crucial Potentiator for Efficient Enzyme Digestion of the Human Pancreas
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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158545/ https://www.ncbi.nlm.nih.gov/pubmed/29945463 http://dx.doi.org/10.1177/0963689718779350 |
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author | Eich, Torsten Ståhle, Magnus Gustafsson, Bengt Horneland, Rune Lempinen, Marko Lundgren, Torbjörn Rafael, Ehab Tufveson, Gunnar von Zur-Mühlen, Bengt Olerud, Johan Scholz, Hanne Korsgren, Olle |
author_facet | Eich, Torsten Ståhle, Magnus Gustafsson, Bengt Horneland, Rune Lempinen, Marko Lundgren, Torbjörn Rafael, Ehab Tufveson, Gunnar von Zur-Mühlen, Bengt Olerud, Johan Scholz, Hanne Korsgren, Olle |
author_sort | Eich, Torsten |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-6158545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-61585452018-10-01 Calcium: A Crucial Potentiator for Efficient Enzyme Digestion of the Human Pancreas Eich, Torsten Ståhle, Magnus Gustafsson, Bengt Horneland, Rune Lempinen, Marko Lundgren, Torbjörn Rafael, Ehab Tufveson, Gunnar von Zur-Mühlen, Bengt Olerud, Johan Scholz, Hanne Korsgren, Olle Cell Transplant Original Articles 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. SAGE Publications 2018-06-26 2018-07 /pmc/articles/PMC6158545/ /pubmed/29945463 http://dx.doi.org/10.1177/0963689718779350 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Articles Eich, Torsten Ståhle, Magnus Gustafsson, Bengt Horneland, Rune Lempinen, Marko Lundgren, Torbjörn Rafael, Ehab Tufveson, Gunnar von Zur-Mühlen, Bengt Olerud, Johan Scholz, Hanne Korsgren, Olle Calcium: A Crucial Potentiator for Efficient Enzyme Digestion of the Human Pancreas |
title | Calcium: A Crucial Potentiator for Efficient Enzyme Digestion of the Human Pancreas |
title_full | Calcium: A Crucial Potentiator for Efficient Enzyme Digestion of the Human Pancreas |
title_fullStr | Calcium: A Crucial Potentiator for Efficient Enzyme Digestion of the Human Pancreas |
title_full_unstemmed | Calcium: A Crucial Potentiator for Efficient Enzyme Digestion of the Human Pancreas |
title_short | Calcium: A Crucial Potentiator for Efficient Enzyme Digestion of the Human Pancreas |
title_sort | calcium: a crucial potentiator for efficient enzyme digestion of the human pancreas |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158545/ https://www.ncbi.nlm.nih.gov/pubmed/29945463 http://dx.doi.org/10.1177/0963689718779350 |
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