Pretreatment of crude pancreatic islets with mitomycin C prolongs graft survival time in xenogeneic rat-to-mouse model
Rejection of pancreatic islet grafts is still a serious problem. We evaluated the effect of mitomycin C (MMC) on the survival of crude islets grafts after xenogeneic islet transplantation. WS (RT1k) rat islets pretreated with various concentrations of MMC (0, 1, 3.2, 10, 32, 50, 100, 320, and 1,000...
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| Veröffentlicht in: | Transplantation 1999-06, Vol.67 (11), p.1474-1477 |
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| creator | GROCHOWIECKI, T GOTOH, M KIMURA, F HE, L NAGANO, H NAKAMORI, S UMESHITA, K SAKON, M MONDEN, M DONO, K TAKEDA, Y NISHIHARA, M OHTA, Y OTA, H OHZATO, H OKUYAMA, M SHIMIZU, J |
| description | Rejection of pancreatic islet grafts is still a serious problem. We evaluated the effect of mitomycin C (MMC) on the survival of crude islets grafts after xenogeneic islet transplantation.
WS (RT1k) rat islets pretreated with various concentrations of MMC (0, 1, 3.2, 10, 32, 50, 100, 320, and 1,000 microg/ml) were transplanted into C57BL/6 mice with streptozotocin-induced diabetes. In vivo graft function was assessed by a daily measurement of nonfasting blood glucose concentration in each animal. We also examined the separate effect of MMC on purified islets and contaminants present in the crude islet preparation.
MMC at doses of 10, 32, 50, and 100 microg/ml resulted in a significant prolongation of the mean graft survival time from a control of 12.4+/-2.5 days to 23+/-7.4, 17.5+/-5.4, 25.5+/-14.7, and 26.7+/-8.9 days, respectively. Deterioration of glucose metabolism was noted when the dose exceeded 32 microg/ml, whereas at 320 microg/ ml, MMC failed to restore normoglycemia. Prolongation of survival time of crude islets was the result of its effect on islets and contaminant components of the crude islet preparation. In vitro study showed that MMC treatment at a higher concentration than 10 microg/ml reduces the stimulatory as well as proliferative capacity of lymph node cells.
Pretreatment of pancreatic islets with MMC at 10 microg/ml prolongs xenograft survival without deterioration of in vivo graft function. This novel treatment modality represents a new strategy for the modulation of immunity of islets and contaminants in crude islet preparations. |
| doi_str_mv | 10.1097/00007890-199906150-00014 |
| format | Article |
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WS (RT1k) rat islets pretreated with various concentrations of MMC (0, 1, 3.2, 10, 32, 50, 100, 320, and 1,000 microg/ml) were transplanted into C57BL/6 mice with streptozotocin-induced diabetes. In vivo graft function was assessed by a daily measurement of nonfasting blood glucose concentration in each animal. We also examined the separate effect of MMC on purified islets and contaminants present in the crude islet preparation.
MMC at doses of 10, 32, 50, and 100 microg/ml resulted in a significant prolongation of the mean graft survival time from a control of 12.4+/-2.5 days to 23+/-7.4, 17.5+/-5.4, 25.5+/-14.7, and 26.7+/-8.9 days, respectively. Deterioration of glucose metabolism was noted when the dose exceeded 32 microg/ml, whereas at 320 microg/ ml, MMC failed to restore normoglycemia. Prolongation of survival time of crude islets was the result of its effect on islets and contaminant components of the crude islet preparation. In vitro study showed that MMC treatment at a higher concentration than 10 microg/ml reduces the stimulatory as well as proliferative capacity of lymph node cells.
Pretreatment of pancreatic islets with MMC at 10 microg/ml prolongs xenograft survival without deterioration of in vivo graft function. This novel treatment modality represents a new strategy for the modulation of immunity of islets and contaminants in crude islet preparations.</description><identifier>ISSN: 0041-1337</identifier><identifier>EISSN: 1534-6080</identifier><identifier>DOI: 10.1097/00007890-199906150-00014</identifier><identifier>PMID: 10385088</identifier><identifier>CODEN: TRPLAU</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animals ; Biological and medical sciences ; Cell Division ; Clinical death. Palliative care. Organ gift and preservation ; Glucose - metabolism ; Graft Survival - drug effects ; Islets of Langerhans - drug effects ; Islets of Langerhans Transplantation - immunology ; Lymph Nodes - cytology ; Male ; Medical sciences ; Mice ; Mitomycin - pharmacology ; Premedication ; Rats ; Transplantation, Heterologous - immunology</subject><ispartof>Transplantation, 1999-06, Vol.67 (11), p.1474-1477</ispartof><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1866376$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10385088$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>GROCHOWIECKI, T</creatorcontrib><creatorcontrib>GOTOH, M</creatorcontrib><creatorcontrib>KIMURA, F</creatorcontrib><creatorcontrib>HE, L</creatorcontrib><creatorcontrib>NAGANO, H</creatorcontrib><creatorcontrib>NAKAMORI, S</creatorcontrib><creatorcontrib>UMESHITA, K</creatorcontrib><creatorcontrib>SAKON, M</creatorcontrib><creatorcontrib>MONDEN, M</creatorcontrib><creatorcontrib>DONO, K</creatorcontrib><creatorcontrib>TAKEDA, Y</creatorcontrib><creatorcontrib>NISHIHARA, M</creatorcontrib><creatorcontrib>OHTA, Y</creatorcontrib><creatorcontrib>OTA, H</creatorcontrib><creatorcontrib>OHZATO, H</creatorcontrib><creatorcontrib>OKUYAMA, M</creatorcontrib><creatorcontrib>SHIMIZU, J</creatorcontrib><title>Pretreatment of crude pancreatic islets with mitomycin C prolongs graft survival time in xenogeneic rat-to-mouse model</title><title>Transplantation</title><addtitle>Transplantation</addtitle><description>Rejection of pancreatic islet grafts is still a serious problem. We evaluated the effect of mitomycin C (MMC) on the survival of crude islets grafts after xenogeneic islet transplantation.
WS (RT1k) rat islets pretreated with various concentrations of MMC (0, 1, 3.2, 10, 32, 50, 100, 320, and 1,000 microg/ml) were transplanted into C57BL/6 mice with streptozotocin-induced diabetes. In vivo graft function was assessed by a daily measurement of nonfasting blood glucose concentration in each animal. We also examined the separate effect of MMC on purified islets and contaminants present in the crude islet preparation.
MMC at doses of 10, 32, 50, and 100 microg/ml resulted in a significant prolongation of the mean graft survival time from a control of 12.4+/-2.5 days to 23+/-7.4, 17.5+/-5.4, 25.5+/-14.7, and 26.7+/-8.9 days, respectively. Deterioration of glucose metabolism was noted when the dose exceeded 32 microg/ml, whereas at 320 microg/ ml, MMC failed to restore normoglycemia. Prolongation of survival time of crude islets was the result of its effect on islets and contaminant components of the crude islet preparation. In vitro study showed that MMC treatment at a higher concentration than 10 microg/ml reduces the stimulatory as well as proliferative capacity of lymph node cells.
Pretreatment of pancreatic islets with MMC at 10 microg/ml prolongs xenograft survival without deterioration of in vivo graft function. This novel treatment modality represents a new strategy for the modulation of immunity of islets and contaminants in crude islet preparations.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Division</subject><subject>Clinical death. Palliative care. Organ gift and preservation</subject><subject>Glucose - metabolism</subject><subject>Graft Survival - drug effects</subject><subject>Islets of Langerhans - drug effects</subject><subject>Islets of Langerhans Transplantation - immunology</subject><subject>Lymph Nodes - cytology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mitomycin - pharmacology</subject><subject>Premedication</subject><subject>Rats</subject><subject>Transplantation, Heterologous - immunology</subject><issn>0041-1337</issn><issn>1534-6080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0E1rGzEQBmARGmLHyV8oOpTelI5Wu_o4FtM0gUB7SM5G1o4chdWuK2md-N9XpQ49di4DLw_DyxBCOdxwMOoL1FHaAOPGGJC8A1YT3p6RJe9EyyRo-ECWAC1nXAi1IJc5v1TSCaUuyIKD0B1ovSSHnwlLQlsijoVOnro090j3dnR_0uBoyAOWTF9DeaYxlCkeXRjpmu7TNEzjLtNdsr7QPKdDONiBlhCRVvGG47TDEeuJZAsrE4vTnJHGqcfhipx7O2S8Pu0Vebr99ri-Yw8_vt-vvz6wfSNVYX0L4KyXCq3cOvB9w7E1TlrtWu2NbnrLG-F6NM53VksQuLWt855L6Aw0YkU-_71b2_6aMZdNDNnhMNgRa5uNNLoTolP_hVwJzjU3FX48wXkbsd_sU4g2HTfvL63g0wnY7OzgU31lyP-cllIoKX4DBUSJbA</recordid><startdate>19990615</startdate><enddate>19990615</enddate><creator>GROCHOWIECKI, T</creator><creator>GOTOH, M</creator><creator>KIMURA, F</creator><creator>HE, L</creator><creator>NAGANO, H</creator><creator>NAKAMORI, S</creator><creator>UMESHITA, K</creator><creator>SAKON, M</creator><creator>MONDEN, M</creator><creator>DONO, K</creator><creator>TAKEDA, Y</creator><creator>NISHIHARA, M</creator><creator>OHTA, Y</creator><creator>OTA, H</creator><creator>OHZATO, H</creator><creator>OKUYAMA, M</creator><creator>SHIMIZU, J</creator><general>Lippincott</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19990615</creationdate><title>Pretreatment of crude pancreatic islets with mitomycin C prolongs graft survival time in xenogeneic rat-to-mouse model</title><author>GROCHOWIECKI, T ; GOTOH, M ; KIMURA, F ; HE, L ; NAGANO, H ; NAKAMORI, S ; UMESHITA, K ; SAKON, M ; MONDEN, M ; DONO, K ; TAKEDA, Y ; NISHIHARA, M ; OHTA, Y ; OTA, H ; OHZATO, H ; OKUYAMA, M ; SHIMIZU, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p267t-d400caf67ea6bc0fd21e49c6a8c48f982da123cde9cf5a8603eba4cff16059023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Division</topic><topic>Clinical death. Palliative care. Organ gift and preservation</topic><topic>Glucose - metabolism</topic><topic>Graft Survival - drug effects</topic><topic>Islets of Langerhans - drug effects</topic><topic>Islets of Langerhans Transplantation - immunology</topic><topic>Lymph Nodes - cytology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mitomycin - pharmacology</topic><topic>Premedication</topic><topic>Rats</topic><topic>Transplantation, Heterologous - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GROCHOWIECKI, T</creatorcontrib><creatorcontrib>GOTOH, M</creatorcontrib><creatorcontrib>KIMURA, F</creatorcontrib><creatorcontrib>HE, L</creatorcontrib><creatorcontrib>NAGANO, H</creatorcontrib><creatorcontrib>NAKAMORI, S</creatorcontrib><creatorcontrib>UMESHITA, K</creatorcontrib><creatorcontrib>SAKON, M</creatorcontrib><creatorcontrib>MONDEN, M</creatorcontrib><creatorcontrib>DONO, K</creatorcontrib><creatorcontrib>TAKEDA, Y</creatorcontrib><creatorcontrib>NISHIHARA, M</creatorcontrib><creatorcontrib>OHTA, Y</creatorcontrib><creatorcontrib>OTA, H</creatorcontrib><creatorcontrib>OHZATO, H</creatorcontrib><creatorcontrib>OKUYAMA, M</creatorcontrib><creatorcontrib>SHIMIZU, J</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>GROCHOWIECKI, T</au><au>GOTOH, M</au><au>KIMURA, F</au><au>HE, L</au><au>NAGANO, H</au><au>NAKAMORI, S</au><au>UMESHITA, K</au><au>SAKON, M</au><au>MONDEN, M</au><au>DONO, K</au><au>TAKEDA, Y</au><au>NISHIHARA, M</au><au>OHTA, Y</au><au>OTA, H</au><au>OHZATO, H</au><au>OKUYAMA, M</au><au>SHIMIZU, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pretreatment of crude pancreatic islets with mitomycin C prolongs graft survival time in xenogeneic rat-to-mouse model</atitle><jtitle>Transplantation</jtitle><addtitle>Transplantation</addtitle><date>1999-06-15</date><risdate>1999</risdate><volume>67</volume><issue>11</issue><spage>1474</spage><epage>1477</epage><pages>1474-1477</pages><issn>0041-1337</issn><eissn>1534-6080</eissn><coden>TRPLAU</coden><abstract>Rejection of pancreatic islet grafts is still a serious problem. We evaluated the effect of mitomycin C (MMC) on the survival of crude islets grafts after xenogeneic islet transplantation.
WS (RT1k) rat islets pretreated with various concentrations of MMC (0, 1, 3.2, 10, 32, 50, 100, 320, and 1,000 microg/ml) were transplanted into C57BL/6 mice with streptozotocin-induced diabetes. In vivo graft function was assessed by a daily measurement of nonfasting blood glucose concentration in each animal. We also examined the separate effect of MMC on purified islets and contaminants present in the crude islet preparation.
MMC at doses of 10, 32, 50, and 100 microg/ml resulted in a significant prolongation of the mean graft survival time from a control of 12.4+/-2.5 days to 23+/-7.4, 17.5+/-5.4, 25.5+/-14.7, and 26.7+/-8.9 days, respectively. Deterioration of glucose metabolism was noted when the dose exceeded 32 microg/ml, whereas at 320 microg/ ml, MMC failed to restore normoglycemia. Prolongation of survival time of crude islets was the result of its effect on islets and contaminant components of the crude islet preparation. In vitro study showed that MMC treatment at a higher concentration than 10 microg/ml reduces the stimulatory as well as proliferative capacity of lymph node cells.
Pretreatment of pancreatic islets with MMC at 10 microg/ml prolongs xenograft survival without deterioration of in vivo graft function. This novel treatment modality represents a new strategy for the modulation of immunity of islets and contaminants in crude islet preparations.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott</pub><pmid>10385088</pmid><doi>10.1097/00007890-199906150-00014</doi><tpages>4</tpages></addata></record> |
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| subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Animals Biological and medical sciences Cell Division Clinical death. Palliative care. Organ gift and preservation Glucose - metabolism Graft Survival - drug effects Islets of Langerhans - drug effects Islets of Langerhans Transplantation - immunology Lymph Nodes - cytology Male Medical sciences Mice Mitomycin - pharmacology Premedication Rats Transplantation, Heterologous - immunology |
| title | Pretreatment of crude pancreatic islets with mitomycin C prolongs graft survival time in xenogeneic rat-to-mouse model |
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