A DNA hybridization system for labeling of neural stem cells with SPIO nanoparticles for MRI monitoring post-transplantation
Abstract Neural stem cells (NSCs) demonstrate encouraging results in cell replacement therapy for neurodegenerative disorders and traumatic injury in the central nervous system. Monitor the survival and migration of transplanted cells would provide us important information concerning the performance...
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Veröffentlicht in: | Biomaterials 2015-06, Vol.54, p.158-167 |
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description | Abstract Neural stem cells (NSCs) demonstrate encouraging results in cell replacement therapy for neurodegenerative disorders and traumatic injury in the central nervous system. Monitor the survival and migration of transplanted cells would provide us important information concerning the performance and integration of the graft during the therapy time course. Magnetic resonance imaging (MRI) allow us to monitor the transplanted cells in a non-invasive way. The only requirement is to use an appropriate contrast agent to label the transplanted cells. Superparamagnetic iron oxide (SPIO) nanoparticles are one of the most commonly used contrast agent for MRI detection of transplanted cells. SPIO nanoparticles demonstrated to be suitable for labeling several types of cells including NSCs. However, the current methods for SPIO labeling are non-specific, depending mostly on electrostatic interactions, demanding relatively high SPIO concentration, and long incubation time, which can affect the viability of cells. In this study, we propose a specific and relatively fast method to label NSCs with SPIO nanoparticles via DNA hybridization. Two short single stranded DNAs (ssDNAs), oligo[dT]20 and oligo[dA]20 were conjugated with a lipid molecule and SPIO nanoparticle respectively. The labeling process comprises two simple steps; first the cells are modified to present oligo[dT]20 ssDNA on the cell surface, then the oligo[dA]20 ssDNA conjugated with SPIO nanoparticles are presented to the modified cells to allow the oligo[dT]20 -oligo[dA]20 hybridization. The method showed to be non-toxic at concentrations up to 50 μg/mL oligo[dA]20 -SPIO nanoparticles. Presence of SPIO nanoparticles at cell surface and cell cytoplasm was verified by transmission electron microscopy (TEM). SPIO labeling via DNA hybridization demonstrated to not interfere on NSCs proliferation, aggregates formation, and differentiation. NSCs labeled with SPIO nanoparticles via DNA hybridization system were successfully detected by MRI in vitro as well in vivo . Cells transplanted into the rat brain striatum could be detected by MRI scanning up to 1 month post-transplantation. |
doi_str_mv | 10.1016/j.biomaterials.2015.03.017 |
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Monitor the survival and migration of transplanted cells would provide us important information concerning the performance and integration of the graft during the therapy time course. Magnetic resonance imaging (MRI) allow us to monitor the transplanted cells in a non-invasive way. The only requirement is to use an appropriate contrast agent to label the transplanted cells. Superparamagnetic iron oxide (SPIO) nanoparticles are one of the most commonly used contrast agent for MRI detection of transplanted cells. SPIO nanoparticles demonstrated to be suitable for labeling several types of cells including NSCs. However, the current methods for SPIO labeling are non-specific, depending mostly on electrostatic interactions, demanding relatively high SPIO concentration, and long incubation time, which can affect the viability of cells. In this study, we propose a specific and relatively fast method to label NSCs with SPIO nanoparticles via DNA hybridization. Two short single stranded DNAs (ssDNAs), oligo[dT]20 and oligo[dA]20 were conjugated with a lipid molecule and SPIO nanoparticle respectively. The labeling process comprises two simple steps; first the cells are modified to present oligo[dT]20 ssDNA on the cell surface, then the oligo[dA]20 ssDNA conjugated with SPIO nanoparticles are presented to the modified cells to allow the oligo[dT]20 -oligo[dA]20 hybridization. The method showed to be non-toxic at concentrations up to 50 μg/mL oligo[dA]20 -SPIO nanoparticles. Presence of SPIO nanoparticles at cell surface and cell cytoplasm was verified by transmission electron microscopy (TEM). SPIO labeling via DNA hybridization demonstrated to not interfere on NSCs proliferation, aggregates formation, and differentiation. NSCs labeled with SPIO nanoparticles via DNA hybridization system were successfully detected by MRI in vitro as well in vivo . Cells transplanted into the rat brain striatum could be detected by MRI scanning up to 1 month post-transplantation.</description><identifier>ISSN: 0142-9612</identifier><identifier>EISSN: 1878-5905</identifier><identifier>DOI: 10.1016/j.biomaterials.2015.03.017</identifier><identifier>PMID: 25907049</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Advanced Basic Science ; Animals ; Cell Tracking - methods ; Cells, Cultured ; Contrast agents ; Contrast Media ; Dentistry ; Deoxyribonucleic acid ; Dextrans ; DNA Probes - genetics ; In vitro test ; Magnetic resonance imaging ; Magnetic Resonance Imaging - methods ; Magnetite Nanoparticles ; Marking ; Monitors ; MRI (magnetic resonance imaging) ; Nanoparticle ; Nanoparticles ; Neural cell ; Neural Stem Cells - cytology ; Neural Stem Cells - physiology ; Neural Stem Cells - transplantation ; Rats ; Rats, Sprague-Dawley ; Staining and Labeling ; Stem cell ; Surgical implants ; Therapy ; Transplantation</subject><ispartof>Biomaterials, 2015-06, Vol.54, p.158-167</ispartof><rights>Elsevier Ltd</rights><rights>2015 Elsevier Ltd</rights><rights>Copyright © 2015 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c501t-f7bfb467ed1326e686ccbc6ceb54af5a2e4458ffaaed69f7a5ccfc5b6deffe23</citedby><cites>FETCH-LOGICAL-c501t-f7bfb467ed1326e686ccbc6ceb54af5a2e4458ffaaed69f7a5ccfc5b6deffe23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0142961215002872$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25907049$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Egawa, Edgar Y</creatorcontrib><creatorcontrib>Kitamura, Narufumi</creatorcontrib><creatorcontrib>Nakai, Ryusuke</creatorcontrib><creatorcontrib>Arima, Yusuke</creatorcontrib><creatorcontrib>Iwata, Hiroo</creatorcontrib><title>A DNA hybridization system for labeling of neural stem cells with SPIO nanoparticles for MRI monitoring post-transplantation</title><title>Biomaterials</title><addtitle>Biomaterials</addtitle><description>Abstract Neural stem cells (NSCs) demonstrate encouraging results in cell replacement therapy for neurodegenerative disorders and traumatic injury in the central nervous system. Monitor the survival and migration of transplanted cells would provide us important information concerning the performance and integration of the graft during the therapy time course. Magnetic resonance imaging (MRI) allow us to monitor the transplanted cells in a non-invasive way. The only requirement is to use an appropriate contrast agent to label the transplanted cells. Superparamagnetic iron oxide (SPIO) nanoparticles are one of the most commonly used contrast agent for MRI detection of transplanted cells. SPIO nanoparticles demonstrated to be suitable for labeling several types of cells including NSCs. However, the current methods for SPIO labeling are non-specific, depending mostly on electrostatic interactions, demanding relatively high SPIO concentration, and long incubation time, which can affect the viability of cells. In this study, we propose a specific and relatively fast method to label NSCs with SPIO nanoparticles via DNA hybridization. Two short single stranded DNAs (ssDNAs), oligo[dT]20 and oligo[dA]20 were conjugated with a lipid molecule and SPIO nanoparticle respectively. The labeling process comprises two simple steps; first the cells are modified to present oligo[dT]20 ssDNA on the cell surface, then the oligo[dA]20 ssDNA conjugated with SPIO nanoparticles are presented to the modified cells to allow the oligo[dT]20 -oligo[dA]20 hybridization. The method showed to be non-toxic at concentrations up to 50 μg/mL oligo[dA]20 -SPIO nanoparticles. Presence of SPIO nanoparticles at cell surface and cell cytoplasm was verified by transmission electron microscopy (TEM). SPIO labeling via DNA hybridization demonstrated to not interfere on NSCs proliferation, aggregates formation, and differentiation. NSCs labeled with SPIO nanoparticles via DNA hybridization system were successfully detected by MRI in vitro as well in vivo . Cells transplanted into the rat brain striatum could be detected by MRI scanning up to 1 month post-transplantation.</description><subject>Advanced Basic Science</subject><subject>Animals</subject><subject>Cell Tracking - methods</subject><subject>Cells, Cultured</subject><subject>Contrast agents</subject><subject>Contrast Media</subject><subject>Dentistry</subject><subject>Deoxyribonucleic acid</subject><subject>Dextrans</subject><subject>DNA Probes - genetics</subject><subject>In vitro test</subject><subject>Magnetic resonance imaging</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Magnetite Nanoparticles</subject><subject>Marking</subject><subject>Monitors</subject><subject>MRI (magnetic resonance imaging)</subject><subject>Nanoparticle</subject><subject>Nanoparticles</subject><subject>Neural cell</subject><subject>Neural Stem Cells - cytology</subject><subject>Neural Stem Cells - physiology</subject><subject>Neural Stem Cells - transplantation</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Staining and Labeling</subject><subject>Stem cell</subject><subject>Surgical implants</subject><subject>Therapy</subject><subject>Transplantation</subject><issn>0142-9612</issn><issn>1878-5905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkk1v1DAQhi0EokvhLyCLE5cE24nthAPSquVjpUIR7d1ynDH1kthb2wEt4seT7BaEOPVkWX7eGY2fQegFJSUlVLzalp0Lo84QnR5SyQjlJalKQuUDtKKNbAreEv4QrQitWdEKyk7Qk5S2ZL6Tmj1GJ2wGJKnbFfq1xuef1vhm30XXu586u-Bx2qcMI7Yh4kF3MDj_FQeLPUxRD_jwZmAYEv7h8g2--ry5xF77sNMxOzNAOiQ_ftngMXiXQ1zyu5BykaP2aTdonw-NnqJHdp4Ant2dp-j63dvrsw_FxeX7zdn6ojCc0FxY2dmuFhJ6WjEBohHGdEYY6HitLdcM6po31moNvWit1NwYa3gnerAWWHWKXh7L7mK4nSBlNbq0DKA9hCkpKiVhkrG6vQdasYaKWi7o6yNqYkgpglW76EYd94oStXhSW_WvJ7V4UqRSs6c5_Pyuz9SN0P-N_hEzA-dHAOZ_-e4gqmQceAO9i2Cy6oO7X583_5Uxs01n9PAN9pC2YYp-yVCVmCLqatmYZWEoJ4Q1klW_AfeCw4Y</recordid><startdate>20150601</startdate><enddate>20150601</enddate><creator>Egawa, Edgar Y</creator><creator>Kitamura, Narufumi</creator><creator>Nakai, Ryusuke</creator><creator>Arima, Yusuke</creator><creator>Iwata, Hiroo</creator><general>Elsevier Ltd</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>7QO</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>F28</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20150601</creationdate><title>A DNA hybridization system for labeling of neural stem cells with SPIO nanoparticles for MRI monitoring post-transplantation</title><author>Egawa, Edgar Y ; Kitamura, Narufumi ; Nakai, Ryusuke ; Arima, Yusuke ; Iwata, Hiroo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c501t-f7bfb467ed1326e686ccbc6ceb54af5a2e4458ffaaed69f7a5ccfc5b6deffe23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Advanced Basic Science</topic><topic>Animals</topic><topic>Cell Tracking - methods</topic><topic>Cells, Cultured</topic><topic>Contrast agents</topic><topic>Contrast Media</topic><topic>Dentistry</topic><topic>Deoxyribonucleic acid</topic><topic>Dextrans</topic><topic>DNA Probes - genetics</topic><topic>In vitro test</topic><topic>Magnetic resonance imaging</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Magnetite Nanoparticles</topic><topic>Marking</topic><topic>Monitors</topic><topic>MRI (magnetic resonance imaging)</topic><topic>Nanoparticle</topic><topic>Nanoparticles</topic><topic>Neural cell</topic><topic>Neural Stem Cells - cytology</topic><topic>Neural Stem Cells - physiology</topic><topic>Neural Stem Cells - transplantation</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Staining and Labeling</topic><topic>Stem cell</topic><topic>Surgical implants</topic><topic>Therapy</topic><topic>Transplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Egawa, Edgar Y</creatorcontrib><creatorcontrib>Kitamura, Narufumi</creatorcontrib><creatorcontrib>Nakai, Ryusuke</creatorcontrib><creatorcontrib>Arima, Yusuke</creatorcontrib><creatorcontrib>Iwata, Hiroo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Egawa, Edgar Y</au><au>Kitamura, Narufumi</au><au>Nakai, Ryusuke</au><au>Arima, Yusuke</au><au>Iwata, Hiroo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A DNA hybridization system for labeling of neural stem cells with SPIO nanoparticles for MRI monitoring post-transplantation</atitle><jtitle>Biomaterials</jtitle><addtitle>Biomaterials</addtitle><date>2015-06-01</date><risdate>2015</risdate><volume>54</volume><spage>158</spage><epage>167</epage><pages>158-167</pages><issn>0142-9612</issn><eissn>1878-5905</eissn><abstract>Abstract Neural stem cells (NSCs) demonstrate encouraging results in cell replacement therapy for neurodegenerative disorders and traumatic injury in the central nervous system. Monitor the survival and migration of transplanted cells would provide us important information concerning the performance and integration of the graft during the therapy time course. Magnetic resonance imaging (MRI) allow us to monitor the transplanted cells in a non-invasive way. The only requirement is to use an appropriate contrast agent to label the transplanted cells. Superparamagnetic iron oxide (SPIO) nanoparticles are one of the most commonly used contrast agent for MRI detection of transplanted cells. SPIO nanoparticles demonstrated to be suitable for labeling several types of cells including NSCs. However, the current methods for SPIO labeling are non-specific, depending mostly on electrostatic interactions, demanding relatively high SPIO concentration, and long incubation time, which can affect the viability of cells. In this study, we propose a specific and relatively fast method to label NSCs with SPIO nanoparticles via DNA hybridization. Two short single stranded DNAs (ssDNAs), oligo[dT]20 and oligo[dA]20 were conjugated with a lipid molecule and SPIO nanoparticle respectively. The labeling process comprises two simple steps; first the cells are modified to present oligo[dT]20 ssDNA on the cell surface, then the oligo[dA]20 ssDNA conjugated with SPIO nanoparticles are presented to the modified cells to allow the oligo[dT]20 -oligo[dA]20 hybridization. The method showed to be non-toxic at concentrations up to 50 μg/mL oligo[dA]20 -SPIO nanoparticles. Presence of SPIO nanoparticles at cell surface and cell cytoplasm was verified by transmission electron microscopy (TEM). SPIO labeling via DNA hybridization demonstrated to not interfere on NSCs proliferation, aggregates formation, and differentiation. NSCs labeled with SPIO nanoparticles via DNA hybridization system were successfully detected by MRI in vitro as well in vivo . Cells transplanted into the rat brain striatum could be detected by MRI scanning up to 1 month post-transplantation.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>25907049</pmid><doi>10.1016/j.biomaterials.2015.03.017</doi><tpages>10</tpages></addata></record> |
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subjects | Advanced Basic Science Animals Cell Tracking - methods Cells, Cultured Contrast agents Contrast Media Dentistry Deoxyribonucleic acid Dextrans DNA Probes - genetics In vitro test Magnetic resonance imaging Magnetic Resonance Imaging - methods Magnetite Nanoparticles Marking Monitors MRI (magnetic resonance imaging) Nanoparticle Nanoparticles Neural cell Neural Stem Cells - cytology Neural Stem Cells - physiology Neural Stem Cells - transplantation Rats Rats, Sprague-Dawley Staining and Labeling Stem cell Surgical implants Therapy Transplantation |
title | A DNA hybridization system for labeling of neural stem cells with SPIO nanoparticles for MRI monitoring post-transplantation |
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