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In vivo magnetic resonance imaging of injected mesenchymal stem cells in rat myocardial infarction; simultaneous cell tracking and left ventricular function measurement
To determine whether magnetic resonance imaging (MRI) can enable magnetically labeled mesenchymal stem cell (MSC) tracking and simultaneous in vivo functional data acquisition in rat models of myocardial infarction. Superparamagnetic iron oxide-laden human MSCs were injected into rat myocardium infa...
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Published in: | The International Journal of Cardiovascular Imaging 2009-04, Vol.25 (Suppl 1), p.99-109 |
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container_end_page | 109 |
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container_title | The International Journal of Cardiovascular Imaging |
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creator | Kim, Young Jin Huh, Yong-Min Choe, Kyu Ok Choi, Byoung Wook Choi, Eun Jeong Jang, Yangsoo Lee, Jae Myun Suh, Jin-Suck |
description | To determine whether magnetic resonance imaging (MRI) can enable magnetically labeled mesenchymal stem cell (MSC) tracking and simultaneous in vivo functional data acquisition in rat models of myocardial infarction. Superparamagnetic iron oxide-laden human MSCs were injected into rat myocardium infarcted by cryoinjury 3 weeks after myocardial infarction. The control group received cell-free media injection. Before injection and for 3 months after, in vivo serial MRI was performed. Electrocardiography-gated gradient echo sequence MRI and cine MRI were performed for in vivo cell tracking and assessing cardiac function using left ventricular ejection fraction (LVEF), respectively. MRI revealed a persistent signal-void representing iron-laden MSCs until ten post-injection weeks. Serial follow-up MRI revealed that LVEF was significantly higher in the MSC injection group than in the control group. We conclude that MRI enables in vivo tracking of injected cells and evaluation of the long-term therapeutic potential of MSCs for myocardial infarction. |
doi_str_mv | 10.1007/s10554-008-9407-0 |
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Superparamagnetic iron oxide-laden human MSCs were injected into rat myocardium infarcted by cryoinjury 3 weeks after myocardial infarction. The control group received cell-free media injection. Before injection and for 3 months after, in vivo serial MRI was performed. Electrocardiography-gated gradient echo sequence MRI and cine MRI were performed for in vivo cell tracking and assessing cardiac function using left ventricular ejection fraction (LVEF), respectively. MRI revealed a persistent signal-void representing iron-laden MSCs until ten post-injection weeks. Serial follow-up MRI revealed that LVEF was significantly higher in the MSC injection group than in the control group. We conclude that MRI enables in vivo tracking of injected cells and evaluation of the long-term therapeutic potential of MSCs for myocardial infarction.</description><identifier>ISSN: 1569-5794</identifier><identifier>EISSN: 1573-0743</identifier><identifier>EISSN: 1875-8312</identifier><identifier>DOI: 10.1007/s10554-008-9407-0</identifier><identifier>PMID: 19132547</identifier><identifier>CODEN: IJCIBI</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Animals ; Cardiac Imaging ; Cardiology ; Cell Movement ; Cells, Cultured ; Contrast Media ; Dextrans ; Disease Models, Animal ; Electrocardiography ; Ferrosoferric Oxide ; Humans ; Imaging ; Iron ; Magnetic Resonance Imaging, Cine ; Magnetite Nanoparticles ; Male ; Medicine ; Medicine & Public Health ; Mesenchymal Stem Cell Transplantation ; Myocardial Infarction - pathology ; Myocardial Infarction - physiopathology ; Myocardial Infarction - surgery ; Myocardium - pathology ; Original Paper ; Oxides ; Radiology ; Rats ; Rats, Sprague-Dawley ; Stroke Volume ; Time Factors ; Ventricular Function, Left</subject><ispartof>The International Journal of Cardiovascular Imaging, 2009-04, Vol.25 (Suppl 1), p.99-109</ispartof><rights>Springer Science+Business Media, B.V. 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c369t-1521f008fd913aeda0b0575be41451b00cabb8d04803e2067a1f737024cbd64c3</citedby><cites>FETCH-LOGICAL-c369t-1521f008fd913aeda0b0575be41451b00cabb8d04803e2067a1f737024cbd64c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19132547$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Young Jin</creatorcontrib><creatorcontrib>Huh, Yong-Min</creatorcontrib><creatorcontrib>Choe, Kyu Ok</creatorcontrib><creatorcontrib>Choi, Byoung Wook</creatorcontrib><creatorcontrib>Choi, Eun Jeong</creatorcontrib><creatorcontrib>Jang, Yangsoo</creatorcontrib><creatorcontrib>Lee, Jae Myun</creatorcontrib><creatorcontrib>Suh, Jin-Suck</creatorcontrib><title>In vivo magnetic resonance imaging of injected mesenchymal stem cells in rat myocardial infarction; simultaneous cell tracking and left ventricular function measurement</title><title>The International Journal of Cardiovascular Imaging</title><addtitle>Int J Cardiovasc Imaging</addtitle><addtitle>Int J Cardiovasc Imaging</addtitle><description>To determine whether magnetic resonance imaging (MRI) can enable magnetically labeled mesenchymal stem cell (MSC) tracking and simultaneous in vivo functional data acquisition in rat models of myocardial infarction. Superparamagnetic iron oxide-laden human MSCs were injected into rat myocardium infarcted by cryoinjury 3 weeks after myocardial infarction. The control group received cell-free media injection. Before injection and for 3 months after, in vivo serial MRI was performed. Electrocardiography-gated gradient echo sequence MRI and cine MRI were performed for in vivo cell tracking and assessing cardiac function using left ventricular ejection fraction (LVEF), respectively. MRI revealed a persistent signal-void representing iron-laden MSCs until ten post-injection weeks. Serial follow-up MRI revealed that LVEF was significantly higher in the MSC injection group than in the control group. We conclude that MRI enables in vivo tracking of injected cells and evaluation of the long-term therapeutic potential of MSCs for myocardial infarction.</description><subject>Animals</subject><subject>Cardiac Imaging</subject><subject>Cardiology</subject><subject>Cell Movement</subject><subject>Cells, Cultured</subject><subject>Contrast Media</subject><subject>Dextrans</subject><subject>Disease Models, Animal</subject><subject>Electrocardiography</subject><subject>Ferrosoferric Oxide</subject><subject>Humans</subject><subject>Imaging</subject><subject>Iron</subject><subject>Magnetic Resonance Imaging, Cine</subject><subject>Magnetite Nanoparticles</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mesenchymal Stem Cell Transplantation</subject><subject>Myocardial Infarction - pathology</subject><subject>Myocardial Infarction - physiopathology</subject><subject>Myocardial Infarction - surgery</subject><subject>Myocardium - pathology</subject><subject>Original Paper</subject><subject>Oxides</subject><subject>Radiology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Stroke Volume</subject><subject>Time Factors</subject><subject>Ventricular Function, Left</subject><issn>1569-5794</issn><issn>1573-0743</issn><issn>1875-8312</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp1Uctu3CAURVWq5tF-QDYRyt7pBYMZK6soSttIkbpp1wjjy5SJDQngkeaP-pllMiNl1RWI87rcQ8glgxsGoL5mBlKKBmDV9AJUAx_IGZOqbUCJ9mR_7_pGql6ckvOcNwDAgbefyCnrWculUGfk72OgW7-NdDbrgMVbmjDHYIJF6uubD2saHfVhg7bgSGfMGOyf3WwmmgvO1OI05YrTZAqdd9GaNPoK-uBMssXHcEuzn5epmIBxyW8CWpKxz3tvE0Y6oSt0i6Ekb5fJJOqW8KasaSYvCeeKfSYfnZkyfjmeF-T3t4df9z-ap5_fH-_vnhrbdn1pmOTM1YW4sX7R4GhgAKnkgIIJyQYAa4ZhNYJYQYscOmWYU60CLuwwdsK2F-T64PuS4uuCuehNXFKokZrXffKu56yS2IFkU8w5odMvqW4r7TQDva9GH6rRdRK9r0ZD1VwdjZdhxvFdceyiEviBkCsU1pjek__v-g-Gj51x</recordid><startdate>200904</startdate><enddate>200904</enddate><creator>Kim, Young Jin</creator><creator>Huh, Yong-Min</creator><creator>Choe, Kyu Ok</creator><creator>Choi, Byoung Wook</creator><creator>Choi, Eun Jeong</creator><creator>Jang, Yangsoo</creator><creator>Lee, Jae Myun</creator><creator>Suh, Jin-Suck</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7Z</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>200904</creationdate><title>In vivo magnetic resonance imaging of injected mesenchymal stem cells in rat myocardial infarction; simultaneous cell tracking and left ventricular function measurement</title><author>Kim, Young Jin ; Huh, Yong-Min ; Choe, Kyu Ok ; Choi, Byoung Wook ; Choi, Eun Jeong ; Jang, Yangsoo ; Lee, Jae Myun ; Suh, Jin-Suck</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c369t-1521f008fd913aeda0b0575be41451b00cabb8d04803e2067a1f737024cbd64c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Cardiac Imaging</topic><topic>Cardiology</topic><topic>Cell Movement</topic><topic>Cells, Cultured</topic><topic>Contrast Media</topic><topic>Dextrans</topic><topic>Disease Models, Animal</topic><topic>Electrocardiography</topic><topic>Ferrosoferric Oxide</topic><topic>Humans</topic><topic>Imaging</topic><topic>Iron</topic><topic>Magnetic Resonance Imaging, Cine</topic><topic>Magnetite Nanoparticles</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mesenchymal Stem Cell Transplantation</topic><topic>Myocardial Infarction - pathology</topic><topic>Myocardial Infarction - physiopathology</topic><topic>Myocardial Infarction - surgery</topic><topic>Myocardium - pathology</topic><topic>Original Paper</topic><topic>Oxides</topic><topic>Radiology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Stroke Volume</topic><topic>Time Factors</topic><topic>Ventricular Function, Left</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Young Jin</creatorcontrib><creatorcontrib>Huh, Yong-Min</creatorcontrib><creatorcontrib>Choe, Kyu Ok</creatorcontrib><creatorcontrib>Choi, Byoung Wook</creatorcontrib><creatorcontrib>Choi, Eun Jeong</creatorcontrib><creatorcontrib>Jang, Yangsoo</creatorcontrib><creatorcontrib>Lee, Jae Myun</creatorcontrib><creatorcontrib>Suh, Jin-Suck</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>The International Journal of Cardiovascular Imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Young Jin</au><au>Huh, Yong-Min</au><au>Choe, Kyu Ok</au><au>Choi, Byoung Wook</au><au>Choi, Eun Jeong</au><au>Jang, Yangsoo</au><au>Lee, Jae Myun</au><au>Suh, Jin-Suck</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vivo magnetic resonance imaging of injected mesenchymal stem cells in rat myocardial infarction; simultaneous cell tracking and left ventricular function measurement</atitle><jtitle>The International Journal of Cardiovascular Imaging</jtitle><stitle>Int J Cardiovasc Imaging</stitle><addtitle>Int J Cardiovasc Imaging</addtitle><date>2009-04</date><risdate>2009</risdate><volume>25</volume><issue>Suppl 1</issue><spage>99</spage><epage>109</epage><pages>99-109</pages><issn>1569-5794</issn><eissn>1573-0743</eissn><eissn>1875-8312</eissn><coden>IJCIBI</coden><abstract>To determine whether magnetic resonance imaging (MRI) can enable magnetically labeled mesenchymal stem cell (MSC) tracking and simultaneous in vivo functional data acquisition in rat models of myocardial infarction. Superparamagnetic iron oxide-laden human MSCs were injected into rat myocardium infarcted by cryoinjury 3 weeks after myocardial infarction. The control group received cell-free media injection. Before injection and for 3 months after, in vivo serial MRI was performed. Electrocardiography-gated gradient echo sequence MRI and cine MRI were performed for in vivo cell tracking and assessing cardiac function using left ventricular ejection fraction (LVEF), respectively. MRI revealed a persistent signal-void representing iron-laden MSCs until ten post-injection weeks. Serial follow-up MRI revealed that LVEF was significantly higher in the MSC injection group than in the control group. We conclude that MRI enables in vivo tracking of injected cells and evaluation of the long-term therapeutic potential of MSCs for myocardial infarction.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>19132547</pmid><doi>10.1007/s10554-008-9407-0</doi><tpages>11</tpages></addata></record> |
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subjects | Animals Cardiac Imaging Cardiology Cell Movement Cells, Cultured Contrast Media Dextrans Disease Models, Animal Electrocardiography Ferrosoferric Oxide Humans Imaging Iron Magnetic Resonance Imaging, Cine Magnetite Nanoparticles Male Medicine Medicine & Public Health Mesenchymal Stem Cell Transplantation Myocardial Infarction - pathology Myocardial Infarction - physiopathology Myocardial Infarction - surgery Myocardium - pathology Original Paper Oxides Radiology Rats Rats, Sprague-Dawley Stroke Volume Time Factors Ventricular Function, Left |
title | In vivo magnetic resonance imaging of injected mesenchymal stem cells in rat myocardial infarction; simultaneous cell tracking and left ventricular function measurement |
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