Analysis of Large-Scale Nonhuman Primate Islet Isolations
It is important to have clinically relevant large animal models, especially nonhuman primates, to improve the efficacy of islet isolation and transplantation prior to clinical trials. The aim of this study was to improve the efficacy of islet isolation by analyzing large-scale nonhuman primate islet...
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Veröffentlicht in: | Transplantation proceedings 2005-03, Vol.37 (2), p.1317-1321 |
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creator | Matsumoto, S. Iwanaga, Y. Okitsu, T. Noguchi, H. Yonekawa, Y. Tanaka, K. Strong, D.M. Reems, J.A. Gaur, L.K. |
description | It is important to have clinically relevant large animal models, especially nonhuman primates, to improve the efficacy of islet isolation and transplantation prior to clinical trials. The aim of this study was to improve the efficacy of islet isolation by analyzing large-scale nonhuman primate islet isolations.
Sixty-one islet isolations were evaluated using nonhuman primates. An automated isolation method was scaled down for islet isolation. Islet yields of prepurification, postpurification, and postculture, purity of islets, viability of islets, and functionality with glucose stimulation test were assessed. Initially, we analyzed relationships between endpoints then analyzed additional factors for successful islet isolation. Those factors included donor characteristics, the two-layer method (TLM) of pancreas preservation, trypsin inhibition during digestion, and digestion and collection time.
Prepurification islet yields were strongly correlated with postpurification yields and postculture yields. It weakly but significantly correlated with purity, viability, and functionality. The average prepurification yield was 16,267 IE/g with each case divided into either above-average (high-yield group) or below-average groups (low-yield group). In 8 cases, TLM and trypsin inhibition were used and all cases belonged to the high-yield group. There were no significant differences between high- and low-yield groups in terms of donor age, body weight, pancreas weight, and cold ischemic time. The high-yield group had significantly longer digestion times and shorter collection times.
TLM, trypsin inhibition, complete digestion, and quick collections were key for successful islet isolation. Analysis of nonhuman primate islet isolation techniques provided useful information, which should help to improve clinical islet transplantation. |
doi_str_mv | 10.1016/j.transproceed.2004.11.051 |
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Sixty-one islet isolations were evaluated using nonhuman primates. An automated isolation method was scaled down for islet isolation. Islet yields of prepurification, postpurification, and postculture, purity of islets, viability of islets, and functionality with glucose stimulation test were assessed. Initially, we analyzed relationships between endpoints then analyzed additional factors for successful islet isolation. Those factors included donor characteristics, the two-layer method (TLM) of pancreas preservation, trypsin inhibition during digestion, and digestion and collection time.
Prepurification islet yields were strongly correlated with postpurification yields and postculture yields. It weakly but significantly correlated with purity, viability, and functionality. The average prepurification yield was 16,267 IE/g with each case divided into either above-average (high-yield group) or below-average groups (low-yield group). In 8 cases, TLM and trypsin inhibition were used and all cases belonged to the high-yield group. There were no significant differences between high- and low-yield groups in terms of donor age, body weight, pancreas weight, and cold ischemic time. The high-yield group had significantly longer digestion times and shorter collection times.
TLM, trypsin inhibition, complete digestion, and quick collections were key for successful islet isolation. Analysis of nonhuman primate islet isolation techniques provided useful information, which should help to improve clinical islet transplantation.</description><identifier>ISSN: 0041-1345</identifier><identifier>EISSN: 1873-2623</identifier><identifier>DOI: 10.1016/j.transproceed.2004.11.051</identifier><identifier>PMID: 15848709</identifier><identifier>CODEN: TRPPA8</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Animals ; Biological and medical sciences ; Cell Culture Techniques - methods ; Cell Separation - methods ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Ischemia ; Islets of Langerhans - cytology ; Macaca nemestrina ; Medical sciences ; Models, Animal ; Organ Size ; Pancreas - anatomy & histology ; Regression Analysis ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Tissue, organ and graft immunology</subject><ispartof>Transplantation proceedings, 2005-03, Vol.37 (2), p.1317-1321</ispartof><rights>2005 Elsevier Inc.</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-c7f891bd5ea2c581d17380db9b2d1c64cc418734c57958d138490a56bebe12933</citedby><cites>FETCH-LOGICAL-c503t-c7f891bd5ea2c581d17380db9b2d1c64cc418734c57958d138490a56bebe12933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0041134504013417$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>309,310,314,776,780,785,786,3537,23909,23910,25118,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16847185$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15848709$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Matsumoto, S.</creatorcontrib><creatorcontrib>Iwanaga, Y.</creatorcontrib><creatorcontrib>Okitsu, T.</creatorcontrib><creatorcontrib>Noguchi, H.</creatorcontrib><creatorcontrib>Yonekawa, Y.</creatorcontrib><creatorcontrib>Tanaka, K.</creatorcontrib><creatorcontrib>Strong, D.M.</creatorcontrib><creatorcontrib>Reems, J.A.</creatorcontrib><creatorcontrib>Gaur, L.K.</creatorcontrib><title>Analysis of Large-Scale Nonhuman Primate Islet Isolations</title><title>Transplantation proceedings</title><addtitle>Transplant Proc</addtitle><description>It is important to have clinically relevant large animal models, especially nonhuman primates, to improve the efficacy of islet isolation and transplantation prior to clinical trials. The aim of this study was to improve the efficacy of islet isolation by analyzing large-scale nonhuman primate islet isolations.
Sixty-one islet isolations were evaluated using nonhuman primates. An automated isolation method was scaled down for islet isolation. Islet yields of prepurification, postpurification, and postculture, purity of islets, viability of islets, and functionality with glucose stimulation test were assessed. Initially, we analyzed relationships between endpoints then analyzed additional factors for successful islet isolation. Those factors included donor characteristics, the two-layer method (TLM) of pancreas preservation, trypsin inhibition during digestion, and digestion and collection time.
Prepurification islet yields were strongly correlated with postpurification yields and postculture yields. It weakly but significantly correlated with purity, viability, and functionality. The average prepurification yield was 16,267 IE/g with each case divided into either above-average (high-yield group) or below-average groups (low-yield group). In 8 cases, TLM and trypsin inhibition were used and all cases belonged to the high-yield group. There were no significant differences between high- and low-yield groups in terms of donor age, body weight, pancreas weight, and cold ischemic time. The high-yield group had significantly longer digestion times and shorter collection times.
TLM, trypsin inhibition, complete digestion, and quick collections were key for successful islet isolation. Analysis of nonhuman primate islet isolation techniques provided useful information, which should help to improve clinical islet transplantation.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Culture Techniques - methods</subject><subject>Cell Separation - methods</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Ischemia</subject><subject>Islets of Langerhans - cytology</subject><subject>Macaca nemestrina</subject><subject>Medical sciences</subject><subject>Models, Animal</subject><subject>Organ Size</subject><subject>Pancreas - anatomy & histology</subject><subject>Regression Analysis</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Tissue, organ and graft immunology</subject><issn>0041-1345</issn><issn>1873-2623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkF1LwzAUhoMobn78BSmC3rXmNEmTejf8HAwV1OuQpqea0bUz6QT_vRkb6qU3CeE855w3DyGnQDOgUFzMs8GbLix9bxHrLKeUZwAZFbBDxqAkS_MiZ7tkHAuQAuNiRA5CmNP4zjnbJyMQiitJyzEpJ51pv4ILSd8kM-PfMH22psXkoe_eVwvTJU_eLcyAyTS0OMSzb83g-i4ckb3GtAGPt_cheb29ebm6T2ePd9OrySy1grIhtbJRJVS1QJNboaAGyRStq7LKa7AFt5avI3MrZClUDUzxkhpRVFgh5CVjh-R8Mzf-92OFYdALFyy2remwXwVdSCmLMlcRvNyA1vcheGz0ch3df2mgei1Oz_VfcXotTgPoKC42n2y3rKpFrP20bk1F4GwLmBAFNXGQdeGXKxSXoETkrjccRiefDr0O1mFnsXYe7aDr3v0nzzc1vZHh</recordid><startdate>20050301</startdate><enddate>20050301</enddate><creator>Matsumoto, S.</creator><creator>Iwanaga, Y.</creator><creator>Okitsu, T.</creator><creator>Noguchi, H.</creator><creator>Yonekawa, Y.</creator><creator>Tanaka, K.</creator><creator>Strong, D.M.</creator><creator>Reems, J.A.</creator><creator>Gaur, L.K.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20050301</creationdate><title>Analysis of Large-Scale Nonhuman Primate Islet Isolations</title><author>Matsumoto, S. ; Iwanaga, Y. ; Okitsu, T. ; Noguchi, H. ; Yonekawa, Y. ; Tanaka, K. ; Strong, D.M. ; Reems, J.A. ; Gaur, L.K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-c7f891bd5ea2c581d17380db9b2d1c64cc418734c57958d138490a56bebe12933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Culture Techniques - methods</topic><topic>Cell Separation - methods</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Ischemia</topic><topic>Islets of Langerhans - cytology</topic><topic>Macaca nemestrina</topic><topic>Medical sciences</topic><topic>Models, Animal</topic><topic>Organ Size</topic><topic>Pancreas - anatomy & histology</topic><topic>Regression Analysis</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Tissue, organ and graft immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matsumoto, S.</creatorcontrib><creatorcontrib>Iwanaga, Y.</creatorcontrib><creatorcontrib>Okitsu, T.</creatorcontrib><creatorcontrib>Noguchi, H.</creatorcontrib><creatorcontrib>Yonekawa, Y.</creatorcontrib><creatorcontrib>Tanaka, K.</creatorcontrib><creatorcontrib>Strong, D.M.</creatorcontrib><creatorcontrib>Reems, J.A.</creatorcontrib><creatorcontrib>Gaur, L.K.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Transplantation proceedings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matsumoto, S.</au><au>Iwanaga, Y.</au><au>Okitsu, T.</au><au>Noguchi, H.</au><au>Yonekawa, Y.</au><au>Tanaka, K.</au><au>Strong, D.M.</au><au>Reems, J.A.</au><au>Gaur, L.K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of Large-Scale Nonhuman Primate Islet Isolations</atitle><jtitle>Transplantation proceedings</jtitle><addtitle>Transplant Proc</addtitle><date>2005-03-01</date><risdate>2005</risdate><volume>37</volume><issue>2</issue><spage>1317</spage><epage>1321</epage><pages>1317-1321</pages><issn>0041-1345</issn><eissn>1873-2623</eissn><coden>TRPPA8</coden><abstract>It is important to have clinically relevant large animal models, especially nonhuman primates, to improve the efficacy of islet isolation and transplantation prior to clinical trials. The aim of this study was to improve the efficacy of islet isolation by analyzing large-scale nonhuman primate islet isolations.
Sixty-one islet isolations were evaluated using nonhuman primates. An automated isolation method was scaled down for islet isolation. Islet yields of prepurification, postpurification, and postculture, purity of islets, viability of islets, and functionality with glucose stimulation test were assessed. Initially, we analyzed relationships between endpoints then analyzed additional factors for successful islet isolation. Those factors included donor characteristics, the two-layer method (TLM) of pancreas preservation, trypsin inhibition during digestion, and digestion and collection time.
Prepurification islet yields were strongly correlated with postpurification yields and postculture yields. It weakly but significantly correlated with purity, viability, and functionality. The average prepurification yield was 16,267 IE/g with each case divided into either above-average (high-yield group) or below-average groups (low-yield group). In 8 cases, TLM and trypsin inhibition were used and all cases belonged to the high-yield group. There were no significant differences between high- and low-yield groups in terms of donor age, body weight, pancreas weight, and cold ischemic time. The high-yield group had significantly longer digestion times and shorter collection times.
TLM, trypsin inhibition, complete digestion, and quick collections were key for successful islet isolation. Analysis of nonhuman primate islet isolation techniques provided useful information, which should help to improve clinical islet transplantation.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>15848709</pmid><doi>10.1016/j.transproceed.2004.11.051</doi><tpages>5</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Cell Culture Techniques - methods Cell Separation - methods Fundamental and applied biological sciences. Psychology Fundamental immunology Ischemia Islets of Langerhans - cytology Macaca nemestrina Medical sciences Models, Animal Organ Size Pancreas - anatomy & histology Regression Analysis Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Tissue, organ and graft immunology |
title | Analysis of Large-Scale Nonhuman Primate Islet Isolations |
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