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Static magnetic field increases survival rate of dental pulp stem cells during DMSO-free cryopreservation
Successful and efficient cryopreservation of living cells and organs is a key clinical application of regenerative medicine. Recently, magnetic cryopreservation has been reported for intact tooth banking and cryopreservation of dental tissue. The aim of this study was to assess the cryoprotective ef...
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Published in: | Electromagnetic biology and medicine 2015-10, Vol.34 (4), p.302-308 |
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container_title | Electromagnetic biology and medicine |
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creator | Lin, Shu-Li Chang, Wei-Jen Lin, Chun-Yen Hsieh, Sung-Chih Lee, Sheng-Yang Fan, Kang-Hsin Lin, Che-Tong Huang, Haw-Ming |
description | Successful and efficient cryopreservation of living cells and organs is a key clinical application of regenerative medicine. Recently, magnetic cryopreservation has been reported for intact tooth banking and cryopreservation of dental tissue. The aim of this study was to assess the cryoprotective effects of static magnetic fields (SMFs) on human dental pulp stem cells (DPSCs) during cryopreservation. Human DPSCs isolated from extracted teeth were frozen with a 0.4-T or 0.8-T SMF and then stored at −196 °C for 24 h. During freezing, the cells were suspended in freezing media containing with 0, 3 or 10% DMSO. After thawing, the changes in survival rate of the DPSCs were determined by flow cytometry. To understand the possible cryoprotective mechanisms of the SMF, the membrane fluidity of SMF-exposed DPSCs was tested. The results showed that when the freezing medium was DMSO-free, the survival rates of the thawed DPSCs increased 2- or 2.5-fold when the cells were exposed to 0.4-T or 0.8-T SMFs, respectively (p |
doi_str_mv | 10.3109/15368378.2014.919588 |
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Recently, magnetic cryopreservation has been reported for intact tooth banking and cryopreservation of dental tissue. The aim of this study was to assess the cryoprotective effects of static magnetic fields (SMFs) on human dental pulp stem cells (DPSCs) during cryopreservation. Human DPSCs isolated from extracted teeth were frozen with a 0.4-T or 0.8-T SMF and then stored at −196 °C for 24 h. During freezing, the cells were suspended in freezing media containing with 0, 3 or 10% DMSO. After thawing, the changes in survival rate of the DPSCs were determined by flow cytometry. To understand the possible cryoprotective mechanisms of the SMF, the membrane fluidity of SMF-exposed DPSCs was tested. The results showed that when the freezing medium was DMSO-free, the survival rates of the thawed DPSCs increased 2- or 2.5-fold when the cells were exposed to 0.4-T or 0.8-T SMFs, respectively (p < 0.01). In addition, after exposure to the 0.4-T SMF, the fluorescence anisotropy of the DPSCs increased significantly (p < 0.01) in the hydrophilic region. These results show that SMF exposure improved DMSO-free cryopreservation. This phenomenon may be due to the improvement of membrane stability for resisting damage caused by ice crystals during the freezing procedure.</description><identifier>ISSN: 1536-8378</identifier><identifier>EISSN: 1536-8386</identifier><identifier>DOI: 10.3109/15368378.2014.919588</identifier><identifier>PMID: 24856869</identifier><language>eng</language><publisher>England: Informa Healthcare</publisher><subject>Adolescent ; Adult ; Anisotropy ; Cell Differentiation ; Cell Lineage ; Cell Membrane - physiology ; Cell Survival ; Cryobiology ; cryopreservation ; Cryopreservation - methods ; Dental Pulp - cytology ; Dental Pulp - radiation effects ; dental pulp stem cell ; Dimethyl Sulfoxide - chemistry ; Flow Cytometry ; Humans ; Magnetic Fields ; Microscopy, Fluorescence ; static magnetic field ; Stem Cells - cytology ; Stem Cells - radiation effects ; Young Adult</subject><ispartof>Electromagnetic biology and medicine, 2015-10, Vol.34 (4), p.302-308</ispartof><rights>2014 Taylor & Francis. 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-d951d56f593fcb443b8d69e27903a0cdc35e6063730257c22aa02211c9776e803</citedby><cites>FETCH-LOGICAL-c499t-d951d56f593fcb443b8d69e27903a0cdc35e6063730257c22aa02211c9776e803</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/24856869$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lin, Shu-Li</creatorcontrib><creatorcontrib>Chang, Wei-Jen</creatorcontrib><creatorcontrib>Lin, Chun-Yen</creatorcontrib><creatorcontrib>Hsieh, Sung-Chih</creatorcontrib><creatorcontrib>Lee, Sheng-Yang</creatorcontrib><creatorcontrib>Fan, Kang-Hsin</creatorcontrib><creatorcontrib>Lin, Che-Tong</creatorcontrib><creatorcontrib>Huang, Haw-Ming</creatorcontrib><title>Static magnetic field increases survival rate of dental pulp stem cells during DMSO-free cryopreservation</title><title>Electromagnetic biology and medicine</title><addtitle>Electromagn Biol Med</addtitle><description>Successful and efficient cryopreservation of living cells and organs is a key clinical application of regenerative medicine. Recently, magnetic cryopreservation has been reported for intact tooth banking and cryopreservation of dental tissue. The aim of this study was to assess the cryoprotective effects of static magnetic fields (SMFs) on human dental pulp stem cells (DPSCs) during cryopreservation. Human DPSCs isolated from extracted teeth were frozen with a 0.4-T or 0.8-T SMF and then stored at −196 °C for 24 h. During freezing, the cells were suspended in freezing media containing with 0, 3 or 10% DMSO. After thawing, the changes in survival rate of the DPSCs were determined by flow cytometry. To understand the possible cryoprotective mechanisms of the SMF, the membrane fluidity of SMF-exposed DPSCs was tested. The results showed that when the freezing medium was DMSO-free, the survival rates of the thawed DPSCs increased 2- or 2.5-fold when the cells were exposed to 0.4-T or 0.8-T SMFs, respectively (p < 0.01). In addition, after exposure to the 0.4-T SMF, the fluorescence anisotropy of the DPSCs increased significantly (p < 0.01) in the hydrophilic region. These results show that SMF exposure improved DMSO-free cryopreservation. This phenomenon may be due to the improvement of membrane stability for resisting damage caused by ice crystals during the freezing procedure.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Anisotropy</subject><subject>Cell Differentiation</subject><subject>Cell Lineage</subject><subject>Cell Membrane - physiology</subject><subject>Cell Survival</subject><subject>Cryobiology</subject><subject>cryopreservation</subject><subject>Cryopreservation - methods</subject><subject>Dental Pulp - cytology</subject><subject>Dental Pulp - radiation effects</subject><subject>dental pulp stem cell</subject><subject>Dimethyl Sulfoxide - chemistry</subject><subject>Flow Cytometry</subject><subject>Humans</subject><subject>Magnetic Fields</subject><subject>Microscopy, Fluorescence</subject><subject>static magnetic field</subject><subject>Stem Cells - cytology</subject><subject>Stem Cells - radiation effects</subject><subject>Young Adult</subject><issn>1536-8378</issn><issn>1536-8386</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp9kMtu1TAQhi0Eohd4A4S8ZJODHce3FUItUKSiLgpry8ceV0ZJHMbJQeftSXTaLlnNRf_MP_MR8o6zneDMfuRSKCO02bWMdzvLrTTmBTnf2o0RRr18zrU5Ixe1_maMW83Ea3LWdkYqo-w5yfezn3Ogg38YYUtShj7SPAYEX6HSuuAhH3xP0c9AS6IRxnktp6WfaJ1hoAH6vtK4YB4f6PWP-7smIQANeCwTQgU8rA5lfENeJd9XePsYL8mvr19-Xt00t3ffvl99vm1CZ-3cRCt5lCpJK1LYd53Ym6gstNoy4VmIQUhQTAktWCt1aFvvWdtyHqzWCgwTl-TDae-E5c8CdXZDrtuNfoSyVMe14Hr9XcpV2p2kAUutCMlNmAePR8eZ2yC7J8hug-xOkNex948Oy36A-Dz0RHUVfDoJ8pgKDv5vwT662R_7ggn9GHLd1v_H4h9Gv4vx</recordid><startdate>20151002</startdate><enddate>20151002</enddate><creator>Lin, Shu-Li</creator><creator>Chang, Wei-Jen</creator><creator>Lin, Chun-Yen</creator><creator>Hsieh, Sung-Chih</creator><creator>Lee, Sheng-Yang</creator><creator>Fan, Kang-Hsin</creator><creator>Lin, Che-Tong</creator><creator>Huang, Haw-Ming</creator><general>Informa Healthcare</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>7X8</scope></search><sort><creationdate>20151002</creationdate><title>Static magnetic field increases survival rate of dental pulp stem cells during DMSO-free cryopreservation</title><author>Lin, Shu-Li ; Chang, Wei-Jen ; Lin, Chun-Yen ; Hsieh, Sung-Chih ; Lee, Sheng-Yang ; Fan, Kang-Hsin ; Lin, Che-Tong ; Huang, Haw-Ming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c499t-d951d56f593fcb443b8d69e27903a0cdc35e6063730257c22aa02211c9776e803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Anisotropy</topic><topic>Cell Differentiation</topic><topic>Cell Lineage</topic><topic>Cell Membrane - physiology</topic><topic>Cell Survival</topic><topic>Cryobiology</topic><topic>cryopreservation</topic><topic>Cryopreservation - methods</topic><topic>Dental Pulp - cytology</topic><topic>Dental Pulp - radiation effects</topic><topic>dental pulp stem cell</topic><topic>Dimethyl Sulfoxide - chemistry</topic><topic>Flow Cytometry</topic><topic>Humans</topic><topic>Magnetic Fields</topic><topic>Microscopy, Fluorescence</topic><topic>static magnetic field</topic><topic>Stem Cells - cytology</topic><topic>Stem Cells - radiation effects</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lin, Shu-Li</creatorcontrib><creatorcontrib>Chang, Wei-Jen</creatorcontrib><creatorcontrib>Lin, Chun-Yen</creatorcontrib><creatorcontrib>Hsieh, Sung-Chih</creatorcontrib><creatorcontrib>Lee, Sheng-Yang</creatorcontrib><creatorcontrib>Fan, Kang-Hsin</creatorcontrib><creatorcontrib>Lin, Che-Tong</creatorcontrib><creatorcontrib>Huang, Haw-Ming</creatorcontrib><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>Electromagnetic biology and medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lin, Shu-Li</au><au>Chang, Wei-Jen</au><au>Lin, Chun-Yen</au><au>Hsieh, Sung-Chih</au><au>Lee, Sheng-Yang</au><au>Fan, Kang-Hsin</au><au>Lin, Che-Tong</au><au>Huang, Haw-Ming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Static magnetic field increases survival rate of dental pulp stem cells during DMSO-free cryopreservation</atitle><jtitle>Electromagnetic biology and medicine</jtitle><addtitle>Electromagn Biol Med</addtitle><date>2015-10-02</date><risdate>2015</risdate><volume>34</volume><issue>4</issue><spage>302</spage><epage>308</epage><pages>302-308</pages><issn>1536-8378</issn><eissn>1536-8386</eissn><abstract>Successful and efficient cryopreservation of living cells and organs is a key clinical application of regenerative medicine. Recently, magnetic cryopreservation has been reported for intact tooth banking and cryopreservation of dental tissue. The aim of this study was to assess the cryoprotective effects of static magnetic fields (SMFs) on human dental pulp stem cells (DPSCs) during cryopreservation. Human DPSCs isolated from extracted teeth were frozen with a 0.4-T or 0.8-T SMF and then stored at −196 °C for 24 h. During freezing, the cells were suspended in freezing media containing with 0, 3 or 10% DMSO. After thawing, the changes in survival rate of the DPSCs were determined by flow cytometry. To understand the possible cryoprotective mechanisms of the SMF, the membrane fluidity of SMF-exposed DPSCs was tested. The results showed that when the freezing medium was DMSO-free, the survival rates of the thawed DPSCs increased 2- or 2.5-fold when the cells were exposed to 0.4-T or 0.8-T SMFs, respectively (p < 0.01). In addition, after exposure to the 0.4-T SMF, the fluorescence anisotropy of the DPSCs increased significantly (p < 0.01) in the hydrophilic region. These results show that SMF exposure improved DMSO-free cryopreservation. This phenomenon may be due to the improvement of membrane stability for resisting damage caused by ice crystals during the freezing procedure.</abstract><cop>England</cop><pub>Informa Healthcare</pub><pmid>24856869</pmid><doi>10.3109/15368378.2014.919588</doi><tpages>7</tpages></addata></record> |
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subjects | Adolescent Adult Anisotropy Cell Differentiation Cell Lineage Cell Membrane - physiology Cell Survival Cryobiology cryopreservation Cryopreservation - methods Dental Pulp - cytology Dental Pulp - radiation effects dental pulp stem cell Dimethyl Sulfoxide - chemistry Flow Cytometry Humans Magnetic Fields Microscopy, Fluorescence static magnetic field Stem Cells - cytology Stem Cells - radiation effects Young Adult |
title | Static magnetic field increases survival rate of dental pulp stem cells during DMSO-free cryopreservation |
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