Islet graft response to transplantation injury includes up-regulation of protective as well as apoptotic genes
Pancreatic islets are particularly vulnerable in the initial days after transplantation when multiple factors converge to damage the islet graft. The aim of this study was to investigate the expression profile of genes involved in damage and protection of beta-cells in the initial days after syngene...
| Autores: | , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2008 |
| País: | España |
| Institución: | Universidad de Barcelona |
| Repositorio: | Dipòsit Digital de la UB |
| OAI Identifier: | oai:diposit.ub.edu:2445/134788 |
| Acceso en línea: | https://hdl.handle.net/2445/134788 |
| Access Level: | acceso abierto |
| Palabra clave: | Gens Apoptosi Expressió gènica Illots de Langerhans Metabolisme Genes Apoptosis Gene expression Islands of Langerhans Metabolism |
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Islet graft response to transplantation injury includes up-regulation of protective as well as apoptotic genesRodríguez-Mulero, SilviaMontanya Mias, EduardGensApoptosiExpressió gènicaIllots de LangerhansMetabolismeGenesApoptosisGene expressionIslands of LangerhansMetabolismPancreatic islets are particularly vulnerable in the initial days after transplantation when multiple factors converge to damage the islet graft. The aim of this study was to investigate the expression profile of genes involved in damage and protection of beta-cells in the initial days after syngeneic islet transplantation. We studied the expression of a set of selected genes involved in apoptosis (Bcl2, Bclx(L), Bax, Bad, Bid, and CHOP), cytokine defense, (SOCS-1 and SOCS-3), or free radical protection (Hmox1, Cu/Zn-SOD, Mn-SOD, and Hsp70). Because hyperglycemia has deleterious effects on islet transplantation outcome, we studied its effect on the expression of these genes. Five hundred islets were syngeneically transplanted under the kidney capsule of normoglycemic or streptozotocin-induced diabetic Lewis rats. Gene expression was analyzed by quantitative real-time RT-PCR in grafts 1, 3, and 7 days after transplantation, and in freshly isolated islets. The expression of proapoptotic genes Bid and CHOP, as well as protective genes Bclx(L), Socs1, Socs3, Hmox1, and MnSod, was maximally increased 1 day after transplantation, and in most cases it remained increased 7 days later, indicating the presence of a protective response against cell damage. In contrast, the expression of Bcl2, Bax, Bad, Cu/ZnSod, and Hsp70 genes did not change. Hyperglycemia did not modify the expression of most studied genes. However, MnSod and Ins2 expression was increased and reduced, respectively, on day 7 after transplantation to diabetic recipients, suggesting that hyperglycemia increased oxidative stress and deteriorated beta-cell function in transplanted islets.Cognizant Communication Corporation2008info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://hdl.handle.net/2445/134788Articles publicats en revistes (Ciències Clíniques)reponame:Dipòsit Digital de la UBinstname:Universidad de BarcelonaInglésReproducció del document publicat a: https://doi.org/10.3727/096368908786991524Cell Transplantation, 2008, vol. 17, num. 9, p. 1025-1034https://doi.org/10.3727/096368908786991524cc-by-nc (c) Cognizant Communication Corporation, 2008http://creativecommons.org/licenses/by-nc/3.0/esinfo:eu-repo/semantics/openAccessoai:diposit.ub.edu:2445/1347882026-05-27T06:46:51Z |
| dc.title.none.fl_str_mv |
Islet graft response to transplantation injury includes up-regulation of protective as well as apoptotic genes |
| title |
Islet graft response to transplantation injury includes up-regulation of protective as well as apoptotic genes |
| spellingShingle |
Islet graft response to transplantation injury includes up-regulation of protective as well as apoptotic genes Rodríguez-Mulero, Silvia Gens Apoptosi Expressió gènica Illots de Langerhans Metabolisme Genes Apoptosis Gene expression Islands of Langerhans Metabolism |
| title_short |
Islet graft response to transplantation injury includes up-regulation of protective as well as apoptotic genes |
| title_full |
Islet graft response to transplantation injury includes up-regulation of protective as well as apoptotic genes |
| title_fullStr |
Islet graft response to transplantation injury includes up-regulation of protective as well as apoptotic genes |
| title_full_unstemmed |
Islet graft response to transplantation injury includes up-regulation of protective as well as apoptotic genes |
| title_sort |
Islet graft response to transplantation injury includes up-regulation of protective as well as apoptotic genes |
| dc.creator.none.fl_str_mv |
Rodríguez-Mulero, Silvia Montanya Mias, Eduard |
| author |
Rodríguez-Mulero, Silvia |
| author_facet |
Rodríguez-Mulero, Silvia Montanya Mias, Eduard |
| author_role |
author |
| author2 |
Montanya Mias, Eduard |
| author2_role |
author |
| dc.subject.none.fl_str_mv |
Gens Apoptosi Expressió gènica Illots de Langerhans Metabolisme Genes Apoptosis Gene expression Islands of Langerhans Metabolism |
| topic |
Gens Apoptosi Expressió gènica Illots de Langerhans Metabolisme Genes Apoptosis Gene expression Islands of Langerhans Metabolism |
| description |
Pancreatic islets are particularly vulnerable in the initial days after transplantation when multiple factors converge to damage the islet graft. The aim of this study was to investigate the expression profile of genes involved in damage and protection of beta-cells in the initial days after syngeneic islet transplantation. We studied the expression of a set of selected genes involved in apoptosis (Bcl2, Bclx(L), Bax, Bad, Bid, and CHOP), cytokine defense, (SOCS-1 and SOCS-3), or free radical protection (Hmox1, Cu/Zn-SOD, Mn-SOD, and Hsp70). Because hyperglycemia has deleterious effects on islet transplantation outcome, we studied its effect on the expression of these genes. Five hundred islets were syngeneically transplanted under the kidney capsule of normoglycemic or streptozotocin-induced diabetic Lewis rats. Gene expression was analyzed by quantitative real-time RT-PCR in grafts 1, 3, and 7 days after transplantation, and in freshly isolated islets. The expression of proapoptotic genes Bid and CHOP, as well as protective genes Bclx(L), Socs1, Socs3, Hmox1, and MnSod, was maximally increased 1 day after transplantation, and in most cases it remained increased 7 days later, indicating the presence of a protective response against cell damage. In contrast, the expression of Bcl2, Bax, Bad, Cu/ZnSod, and Hsp70 genes did not change. Hyperglycemia did not modify the expression of most studied genes. However, MnSod and Ins2 expression was increased and reduced, respectively, on day 7 after transplantation to diabetic recipients, suggesting that hyperglycemia increased oxidative stress and deteriorated beta-cell function in transplanted islets. |
| publishDate |
2008 |
| dc.date.none.fl_str_mv |
2008 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/2445/134788 |
| url |
https://hdl.handle.net/2445/134788 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Reproducció del document publicat a: https://doi.org/10.3727/096368908786991524 Cell Transplantation, 2008, vol. 17, num. 9, p. 1025-1034 https://doi.org/10.3727/096368908786991524 |
| dc.rights.none.fl_str_mv |
cc-by-nc (c) Cognizant Communication Corporation, 2008 http://creativecommons.org/licenses/by-nc/3.0/es info:eu-repo/semantics/openAccess |
| rights_invalid_str_mv |
cc-by-nc (c) Cognizant Communication Corporation, 2008 http://creativecommons.org/licenses/by-nc/3.0/es |
| eu_rights_str_mv |
openAccess |
| dc.format.none.fl_str_mv |
application/pdf |
| dc.publisher.none.fl_str_mv |
Cognizant Communication Corporation |
| publisher.none.fl_str_mv |
Cognizant Communication Corporation |
| dc.source.none.fl_str_mv |
Articles publicats en revistes (Ciències Clíniques) reponame:Dipòsit Digital de la UB instname:Universidad de Barcelona |
| instname_str |
Universidad de Barcelona |
| reponame_str |
Dipòsit Digital de la UB |
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Dipòsit Digital de la UB |
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1869411006285873152 |
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15,300719 |