Alpha-Melanocyte Stimulating Hormone Preserves Islet Graft Survival Through Down-Regulation of Toll-Like Receptors
Abstract The induction of Toll-like receptors (TLRs) in β cells is involved in β-cell death and graft rejection after transplantation. This study investigated the ability of alpha-melanocyte stimulating hormone (α-MSH) to protect pancreatic islets and improve graft survival through regulation of TLR...
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description | Abstract The induction of Toll-like receptors (TLRs) in β cells is involved in β-cell death and graft rejection after transplantation. This study investigated the ability of alpha-melanocyte stimulating hormone (α-MSH) to protect pancreatic islets and improve graft survival through regulation of TLRs. To test the effect of α-MSH on TLR regulation, we first isolated pancreatic islets from rats pretreated with/without α-MSH and assayed inflammatory cytokines and insulin release, and measured the expression of TLRs. Pancreatic islets were transplanted into the kidney capsule of a diabetes mellitus (DM) mouse with and without prior injection of α-MSH. The blood glucose levels were measured and TLR4 expression in transplanted kidney tissue was assessed. Islet morphology, including size and total mass, was improved in the α-MSH group compared to the control group. The expression of TLRs as well as nitric oxide and monocyte chemoattractant protein 1 production were decreased in islets isolated from α-MSH–treated rats. In DM mice, the normoglycemic ratio was higher in the α-MSH–treated group than in the sham group. Moreover, the high levels of TLR4 expression observed in DM kidney tissue were significantly decreased in islet-transplanted tissue with α-MSH. This study showed that α-MSH protects pancreatic islets from cell death and dysfunction through downregulation of TLRs. In conclusion, α-MSH could contribute to improved islet graft survival and function in pancreatic islet transplantation. |
doi_str_mv | 10.1016/j.transproceed.2012.02.018 |
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This study investigated the ability of alpha-melanocyte stimulating hormone (α-MSH) to protect pancreatic islets and improve graft survival through regulation of TLRs. To test the effect of α-MSH on TLR regulation, we first isolated pancreatic islets from rats pretreated with/without α-MSH and assayed inflammatory cytokines and insulin release, and measured the expression of TLRs. Pancreatic islets were transplanted into the kidney capsule of a diabetes mellitus (DM) mouse with and without prior injection of α-MSH. The blood glucose levels were measured and TLR4 expression in transplanted kidney tissue was assessed. Islet morphology, including size and total mass, was improved in the α-MSH group compared to the control group. The expression of TLRs as well as nitric oxide and monocyte chemoattractant protein 1 production were decreased in islets isolated from α-MSH–treated rats. In DM mice, the normoglycemic ratio was higher in the α-MSH–treated group than in the sham group. Moreover, the high levels of TLR4 expression observed in DM kidney tissue were significantly decreased in islet-transplanted tissue with α-MSH. This study showed that α-MSH protects pancreatic islets from cell death and dysfunction through downregulation of TLRs. In conclusion, α-MSH could contribute to improved islet graft survival and function in pancreatic islet transplantation.</description><identifier>ISSN: 0041-1345</identifier><identifier>EISSN: 1873-2623</identifier><identifier>DOI: 10.1016/j.transproceed.2012.02.018</identifier><identifier>PMID: 22564632</identifier><identifier>CODEN: TRPPA8</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>alpha-MSH - administration & dosage ; alpha-MSH - pharmacology ; Animals ; Biological and medical sciences ; Blood Glucose - metabolism ; Chemokine CCL2 - metabolism ; Cytokines - metabolism ; Diabetes Mellitus, Experimental - chemically induced ; Diabetes Mellitus, Experimental - immunology ; Diabetes Mellitus, Experimental - metabolism ; Diabetes Mellitus, Experimental - surgery ; Diabetes Mellitus, Type 1 - chemically induced ; Diabetes Mellitus, Type 1 - immunology ; Diabetes Mellitus, Type 1 - metabolism ; Diabetes Mellitus, Type 1 - surgery ; Down-Regulation ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Graft Survival - drug effects ; Inflammation Mediators - metabolism ; Injections, Intraperitoneal ; Insulin - metabolism ; Islets of Langerhans - drug effects ; Islets of Langerhans - immunology ; Islets of Langerhans - metabolism ; Islets of Langerhans - surgery ; Islets of Langerhans Transplantation ; Male ; Medical sciences ; Mice ; Mice, Nude ; Nitric Oxide - metabolism ; Rats ; Rats, Inbred Lew ; Surgery ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Tissue, organ and graft immunology ; Toll-Like Receptors - drug effects ; Toll-Like Receptors - metabolism</subject><ispartof>Transplantation proceedings, 2012-05, Vol.44 (4), p.1086-1090</ispartof><rights>Elsevier Inc.</rights><rights>2012 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-c007569864080478fbd979d4af0a1af05c7351808381ec4add3f4c5f00fa9da63</citedby><cites>FETCH-LOGICAL-c465t-c007569864080478fbd979d4af0a1af05c7351808381ec4add3f4c5f00fa9da63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.transproceed.2012.02.018$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>310,311,315,781,785,790,791,3551,23934,23935,25144,27928,27929,45999</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25943430$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22564632$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jung, E.-J</creatorcontrib><creatorcontrib>Kim, S.-C</creatorcontrib><creatorcontrib>Jeong, S.-H</creatorcontrib><creatorcontrib>Lee, J.-Y</creatorcontrib><creatorcontrib>Han, D.-J</creatorcontrib><title>Alpha-Melanocyte Stimulating Hormone Preserves Islet Graft Survival Through Down-Regulation of Toll-Like Receptors</title><title>Transplantation proceedings</title><addtitle>Transplant Proc</addtitle><description>Abstract The induction of Toll-like receptors (TLRs) in β cells is involved in β-cell death and graft rejection after transplantation. This study investigated the ability of alpha-melanocyte stimulating hormone (α-MSH) to protect pancreatic islets and improve graft survival through regulation of TLRs. To test the effect of α-MSH on TLR regulation, we first isolated pancreatic islets from rats pretreated with/without α-MSH and assayed inflammatory cytokines and insulin release, and measured the expression of TLRs. Pancreatic islets were transplanted into the kidney capsule of a diabetes mellitus (DM) mouse with and without prior injection of α-MSH. The blood glucose levels were measured and TLR4 expression in transplanted kidney tissue was assessed. Islet morphology, including size and total mass, was improved in the α-MSH group compared to the control group. The expression of TLRs as well as nitric oxide and monocyte chemoattractant protein 1 production were decreased in islets isolated from α-MSH–treated rats. In DM mice, the normoglycemic ratio was higher in the α-MSH–treated group than in the sham group. Moreover, the high levels of TLR4 expression observed in DM kidney tissue were significantly decreased in islet-transplanted tissue with α-MSH. This study showed that α-MSH protects pancreatic islets from cell death and dysfunction through downregulation of TLRs. In conclusion, α-MSH could contribute to improved islet graft survival and function in pancreatic islet transplantation.</description><subject>alpha-MSH - administration & dosage</subject><subject>alpha-MSH - pharmacology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood Glucose - metabolism</subject><subject>Chemokine CCL2 - metabolism</subject><subject>Cytokines - metabolism</subject><subject>Diabetes Mellitus, Experimental - chemically induced</subject><subject>Diabetes Mellitus, Experimental - immunology</subject><subject>Diabetes Mellitus, Experimental - metabolism</subject><subject>Diabetes Mellitus, Experimental - surgery</subject><subject>Diabetes Mellitus, Type 1 - chemically induced</subject><subject>Diabetes Mellitus, Type 1 - immunology</subject><subject>Diabetes Mellitus, Type 1 - metabolism</subject><subject>Diabetes Mellitus, Type 1 - surgery</subject><subject>Down-Regulation</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Graft Survival - drug effects</subject><subject>Inflammation Mediators - metabolism</subject><subject>Injections, Intraperitoneal</subject><subject>Insulin - metabolism</subject><subject>Islets of Langerhans - drug effects</subject><subject>Islets of Langerhans - immunology</subject><subject>Islets of Langerhans - metabolism</subject><subject>Islets of Langerhans - surgery</subject><subject>Islets of Langerhans Transplantation</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Nitric Oxide - metabolism</subject><subject>Rats</subject><subject>Rats, Inbred Lew</subject><subject>Surgery</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Tissue, organ and graft immunology</subject><subject>Toll-Like Receptors - drug effects</subject><subject>Toll-Like Receptors - metabolism</subject><issn>0041-1345</issn><issn>1873-2623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkl-LEzEUxQdR3Lr6FSQIgi9Tb_7MTMYHYdnV3YWKsq3PIZu5adNNJzWZqfTbm9ouik_CJSHkd85NDrco3lCYUqD1-_V0iLpP2xgMYjdlQNkUclH5pJhQ2fCS1Yw_LSYAgpaUi-qseJHSGvKZCf68OGOsqkXN2aSIF3670uUX9LoPZj8gmQ9uM3o9uH5JbkLchB7Jt4gJ4w4TuU0eB3IdtR3IfIw7t9OeLFYxjMsVuQo_-_IOl7_loSfBkkXwvpy5ByR3aHA7hJheFs-s9glfnfbz4vvnT4vLm3L29fr28mJWGlFXQ2kAmqpuZS1Agmikve_apu2EtqBpXirT8IpKkFxSNEJ3HbfCVBbA6rbTNT8v3h19c1A_RkyD2rhk0OefYhiTyllSKVjDWEY_HFETQ0oRrdpGt9Fxn6EDV6u1-jtzdchcQS4qs_j1qc94v8l3j9LHkDPw9gToZLS32ci49IerWsEFh8xdHTnMqewcRpWMw95g5yKaQXXB_d97Pv5jY7zrXe78gHtM6zDGPueuqEpZoOaHKTkMCWUADGrgvwC9FbyK</recordid><startdate>20120501</startdate><enddate>20120501</enddate><creator>Jung, E.-J</creator><creator>Kim, S.-C</creator><creator>Jeong, S.-H</creator><creator>Lee, J.-Y</creator><creator>Han, D.-J</creator><general>Elsevier Inc</general><general>Elsevier</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>20120501</creationdate><title>Alpha-Melanocyte Stimulating Hormone Preserves Islet Graft Survival Through Down-Regulation of Toll-Like Receptors</title><author>Jung, E.-J ; Kim, S.-C ; Jeong, S.-H ; Lee, J.-Y ; Han, D.-J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-c007569864080478fbd979d4af0a1af05c7351808381ec4add3f4c5f00fa9da63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>alpha-MSH - administration & dosage</topic><topic>alpha-MSH - pharmacology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blood Glucose - metabolism</topic><topic>Chemokine CCL2 - metabolism</topic><topic>Cytokines - metabolism</topic><topic>Diabetes Mellitus, Experimental - chemically induced</topic><topic>Diabetes Mellitus, Experimental - immunology</topic><topic>Diabetes Mellitus, Experimental - metabolism</topic><topic>Diabetes Mellitus, Experimental - surgery</topic><topic>Diabetes Mellitus, Type 1 - chemically induced</topic><topic>Diabetes Mellitus, Type 1 - immunology</topic><topic>Diabetes Mellitus, Type 1 - metabolism</topic><topic>Diabetes Mellitus, Type 1 - surgery</topic><topic>Down-Regulation</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Graft Survival - drug effects</topic><topic>Inflammation Mediators - metabolism</topic><topic>Injections, Intraperitoneal</topic><topic>Insulin - metabolism</topic><topic>Islets of Langerhans - drug effects</topic><topic>Islets of Langerhans - immunology</topic><topic>Islets of Langerhans - metabolism</topic><topic>Islets of Langerhans - surgery</topic><topic>Islets of Langerhans Transplantation</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>Nitric Oxide - metabolism</topic><topic>Rats</topic><topic>Rats, Inbred Lew</topic><topic>Surgery</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Tissue, organ and graft immunology</topic><topic>Toll-Like Receptors - drug effects</topic><topic>Toll-Like Receptors - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jung, E.-J</creatorcontrib><creatorcontrib>Kim, S.-C</creatorcontrib><creatorcontrib>Jeong, S.-H</creatorcontrib><creatorcontrib>Lee, J.-Y</creatorcontrib><creatorcontrib>Han, D.-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>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Transplantation proceedings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jung, E.-J</au><au>Kim, S.-C</au><au>Jeong, S.-H</au><au>Lee, J.-Y</au><au>Han, D.-J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alpha-Melanocyte Stimulating Hormone Preserves Islet Graft Survival Through Down-Regulation of Toll-Like Receptors</atitle><jtitle>Transplantation proceedings</jtitle><addtitle>Transplant Proc</addtitle><date>2012-05-01</date><risdate>2012</risdate><volume>44</volume><issue>4</issue><spage>1086</spage><epage>1090</epage><pages>1086-1090</pages><issn>0041-1345</issn><eissn>1873-2623</eissn><coden>TRPPA8</coden><abstract>Abstract The induction of Toll-like receptors (TLRs) in β cells is involved in β-cell death and graft rejection after transplantation. This study investigated the ability of alpha-melanocyte stimulating hormone (α-MSH) to protect pancreatic islets and improve graft survival through regulation of TLRs. To test the effect of α-MSH on TLR regulation, we first isolated pancreatic islets from rats pretreated with/without α-MSH and assayed inflammatory cytokines and insulin release, and measured the expression of TLRs. Pancreatic islets were transplanted into the kidney capsule of a diabetes mellitus (DM) mouse with and without prior injection of α-MSH. The blood glucose levels were measured and TLR4 expression in transplanted kidney tissue was assessed. Islet morphology, including size and total mass, was improved in the α-MSH group compared to the control group. The expression of TLRs as well as nitric oxide and monocyte chemoattractant protein 1 production were decreased in islets isolated from α-MSH–treated rats. In DM mice, the normoglycemic ratio was higher in the α-MSH–treated group than in the sham group. Moreover, the high levels of TLR4 expression observed in DM kidney tissue were significantly decreased in islet-transplanted tissue with α-MSH. This study showed that α-MSH protects pancreatic islets from cell death and dysfunction through downregulation of TLRs. In conclusion, α-MSH could contribute to improved islet graft survival and function in pancreatic islet transplantation.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>22564632</pmid><doi>10.1016/j.transproceed.2012.02.018</doi><tpages>5</tpages></addata></record> |
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subjects | alpha-MSH - administration & dosage alpha-MSH - pharmacology Animals Biological and medical sciences Blood Glucose - metabolism Chemokine CCL2 - metabolism Cytokines - metabolism Diabetes Mellitus, Experimental - chemically induced Diabetes Mellitus, Experimental - immunology Diabetes Mellitus, Experimental - metabolism Diabetes Mellitus, Experimental - surgery Diabetes Mellitus, Type 1 - chemically induced Diabetes Mellitus, Type 1 - immunology Diabetes Mellitus, Type 1 - metabolism Diabetes Mellitus, Type 1 - surgery Down-Regulation Fundamental and applied biological sciences. Psychology Fundamental immunology Graft Survival - drug effects Inflammation Mediators - metabolism Injections, Intraperitoneal Insulin - metabolism Islets of Langerhans - drug effects Islets of Langerhans - immunology Islets of Langerhans - metabolism Islets of Langerhans - surgery Islets of Langerhans Transplantation Male Medical sciences Mice Mice, Nude Nitric Oxide - metabolism Rats Rats, Inbred Lew Surgery Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Tissue, organ and graft immunology Toll-Like Receptors - drug effects Toll-Like Receptors - metabolism |
title | Alpha-Melanocyte Stimulating Hormone Preserves Islet Graft Survival Through Down-Regulation of Toll-Like Receptors |
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