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Comparison of Neutral Proteases and Collagenase Class I as Essential Enzymes for Human Islet Isolation

Efficient islet isolation requires synergistic interaction between collagenase class I (CI) and class II (CII). The CI degradation alters the ratio between CI and CII and is responsible for batch-to-batch variations. This study compares the role of neutral protease (NP) plus clostripain (CP) with CI...

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Autores principales: Brandhorst, Heide, Kurfürst, Manfred, Johnson, Paul R., Korsgren, Olle, Brandhorst, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4946504/
https://www.ncbi.nlm.nih.gov/pubmed/27500241
http://dx.doi.org/10.1097/TXD.0000000000000552
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author Brandhorst, Heide
Kurfürst, Manfred
Johnson, Paul R.
Korsgren, Olle
Brandhorst, Daniel
author_facet Brandhorst, Heide
Kurfürst, Manfred
Johnson, Paul R.
Korsgren, Olle
Brandhorst, Daniel
author_sort Brandhorst, Heide
collection PubMed
description Efficient islet isolation requires synergistic interaction between collagenase class I (CI) and class II (CII). The CI degradation alters the ratio between CI and CII and is responsible for batch-to-batch variations. This study compares the role of neutral protease (NP) plus clostripain (CP) with CI as essential enzymes for human islet isolation. METHODS: Human islets were isolated using 4 different enzyme mixtures composed of CII plus either intact (CI-115) or degraded CI (CI-100). Blends were administered either with or without NP/CP. Purified islets were cultured for 3 to 4 days before islet quality assessment. RESULTS: Whereas using intact CI-115 without NP/CP did not significantly reduce islet yield (3429 ± 631 vs 3087 ± 970 islet equivalent/g, nonsignificant), administration of degraded CI-100 without NP/CP decreased islet yield from 3501 ± 580 to 1312 ± 244 islet equivalent/g (P < 0.01), doubled the amount of undigested tissue from 11.8 ± 1.6 to 24.4 ± 1.2% (P < 0.01) and triplicated the percentage of trapped islets from 7.7 ± 2.8 to 22.5 ± 3.6% (P < 0.05). Islet yield did not vary between supplemented CI-115 and CI-100, but was increased using CI-115 when NP/CP was omitted (P < 0.05). A trend toward higher viability and increased secretory insulin response was noted in both CI-100 and CI-115 when NP/CP was not added. CONCLUSIONS: This study suggests that NP/CP can compensate reduced CI activity. Future attempts to optimize enzyme blends should consider the possibility to increase the proportion of collagenase CI to reduce the need for potentially harmful NPs.
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spelling pubmed-49465042016-08-05 Comparison of Neutral Proteases and Collagenase Class I as Essential Enzymes for Human Islet Isolation Brandhorst, Heide Kurfürst, Manfred Johnson, Paul R. Korsgren, Olle Brandhorst, Daniel Transplant Direct Pancreas and Islet Transplantation Efficient islet isolation requires synergistic interaction between collagenase class I (CI) and class II (CII). The CI degradation alters the ratio between CI and CII and is responsible for batch-to-batch variations. This study compares the role of neutral protease (NP) plus clostripain (CP) with CI as essential enzymes for human islet isolation. METHODS: Human islets were isolated using 4 different enzyme mixtures composed of CII plus either intact (CI-115) or degraded CI (CI-100). Blends were administered either with or without NP/CP. Purified islets were cultured for 3 to 4 days before islet quality assessment. RESULTS: Whereas using intact CI-115 without NP/CP did not significantly reduce islet yield (3429 ± 631 vs 3087 ± 970 islet equivalent/g, nonsignificant), administration of degraded CI-100 without NP/CP decreased islet yield from 3501 ± 580 to 1312 ± 244 islet equivalent/g (P < 0.01), doubled the amount of undigested tissue from 11.8 ± 1.6 to 24.4 ± 1.2% (P < 0.01) and triplicated the percentage of trapped islets from 7.7 ± 2.8 to 22.5 ± 3.6% (P < 0.05). Islet yield did not vary between supplemented CI-115 and CI-100, but was increased using CI-115 when NP/CP was omitted (P < 0.05). A trend toward higher viability and increased secretory insulin response was noted in both CI-100 and CI-115 when NP/CP was not added. CONCLUSIONS: This study suggests that NP/CP can compensate reduced CI activity. Future attempts to optimize enzyme blends should consider the possibility to increase the proportion of collagenase CI to reduce the need for potentially harmful NPs. Lippincott Williams & Wilkins 2015-12-15 /pmc/articles/PMC4946504/ /pubmed/27500241 http://dx.doi.org/10.1097/TXD.0000000000000552 Text en Copyright © 2015 The Authors. Transplantation Direct. Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially.
spellingShingle Pancreas and Islet Transplantation
Brandhorst, Heide
Kurfürst, Manfred
Johnson, Paul R.
Korsgren, Olle
Brandhorst, Daniel
Comparison of Neutral Proteases and Collagenase Class I as Essential Enzymes for Human Islet Isolation
title Comparison of Neutral Proteases and Collagenase Class I as Essential Enzymes for Human Islet Isolation
title_full Comparison of Neutral Proteases and Collagenase Class I as Essential Enzymes for Human Islet Isolation
title_fullStr Comparison of Neutral Proteases and Collagenase Class I as Essential Enzymes for Human Islet Isolation
title_full_unstemmed Comparison of Neutral Proteases and Collagenase Class I as Essential Enzymes for Human Islet Isolation
title_short Comparison of Neutral Proteases and Collagenase Class I as Essential Enzymes for Human Islet Isolation
title_sort comparison of neutral proteases and collagenase class i as essential enzymes for human islet isolation
topic Pancreas and Islet Transplantation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4946504/
https://www.ncbi.nlm.nih.gov/pubmed/27500241
http://dx.doi.org/10.1097/TXD.0000000000000552
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