Characterization of mouse clonal mesenchymal stem cell lines established by subfractionation culturing method
AIM:To characterize single-cell-derived mouse clonal mesenchymal stem cells (mcMSCs) established with bone marrow samples from three different mouse strains. METHODS:We established mcMSC lines using subfractionation culturing method from bone marrow samples obtained from long bones.These lines were...
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Veröffentlicht in: | World journal of stem cells 2011-08, Vol.3 (8), p.70-82 |
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creator | Jeon, Myung-Shin Yi, Tac-Ghee Lim, Hyun-Ja Moon, Sun-Hwa Lee, Moon-Hee Kang, Joon-Soon Kim, Chul-Soo Lee, Dae-Hyun Song, Sun U |
description | AIM:To characterize single-cell-derived mouse clonal mesenchymal stem cells (mcMSCs) established with bone marrow samples from three different mouse strains. METHODS:We established mcMSC lines using subfractionation culturing method from bone marrow samples obtained from long bones.These lines were characterized by measuring cell growth, cell surface epitopes, differentiation potential, lineage-specific gene expression and T-cell suppression capability. Nonclonal MSCs isolated by the conventional gradient centrifugation method were used as controls. RESULTS:All mcMSC lines showed typical nonclonal MSC-like spindle shape morphology. Lines differed inoptimal growth density requirement.Cell surface epitope prof iles of these mcMSC lines were similar to those of nonclonal MSCs. However, some lines exhibited different expression levels in a few epitopes, such as CD44 and CD105. Differentiation assays showed that 90% of the mcMSC lines were capable of differentiating into adipogenic and/or chondrogenic lineages, but only 20% showed osteogenic lineage differentiation. T-cell suppression analysis showed that 75% of the lines exhibited T-cell suppression capability. CONCLUSION:mcMSC lines have similar cell morphology and cell growth rate but exhibit variations in their cell surface epitopes, differentiation potential, lineage-specifi c gene expression and T-cell suppression capability. |
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METHODS:We established mcMSC lines using subfractionation culturing method from bone marrow samples obtained from long bones.These lines were characterized by measuring cell growth, cell surface epitopes, differentiation potential, lineage-specific gene expression and T-cell suppression capability. Nonclonal MSCs isolated by the conventional gradient centrifugation method were used as controls. RESULTS:All mcMSC lines showed typical nonclonal MSC-like spindle shape morphology. Lines differed inoptimal growth density requirement.Cell surface epitope prof iles of these mcMSC lines were similar to those of nonclonal MSCs. However, some lines exhibited different expression levels in a few epitopes, such as CD44 and CD105. Differentiation assays showed that 90% of the mcMSC lines were capable of differentiating into adipogenic and/or chondrogenic lineages, but only 20% showed osteogenic lineage differentiation. T-cell suppression analysis showed that 75% of the lines exhibited T-cell suppression capability. CONCLUSION:mcMSC lines have similar cell morphology and cell growth rate but exhibit variations in their cell surface epitopes, differentiation potential, lineage-specifi c gene expression and T-cell suppression capability.</description><identifier>ISSN: 1948-0210</identifier><identifier>EISSN: 1948-0210</identifier><identifier>DOI: 10.4252/wjsc.v3.i8.70</identifier><identifier>PMID: 22007272</identifier><language>eng</language><publisher>United States: Baishideng Publishing Group Co., Limited</publisher><subject>Bone ; cell ; cells ; Clonal ; differentiation ; isolation ; marrow ; Multilineage ; Original ; stem ; stromal ; suppression ; T-cell</subject><ispartof>World journal of stem cells, 2011-08, Vol.3 (8), p.70-82</ispartof><rights>2011 Baishideng Publishing Group Co., Limited. All rights reserved. 2011</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3250-a4fa2d2476a951cc61d547c6606a661762ca04bc27e1fe4a1bee8b2f83b4b5283</citedby><cites>FETCH-LOGICAL-c3250-a4fa2d2476a951cc61d547c6606a661762ca04bc27e1fe4a1bee8b2f83b4b5283</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/71424X/71424X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3192225/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3192225/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,729,782,786,887,27931,27932,53798,53800</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22007272$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jeon, Myung-Shin</creatorcontrib><creatorcontrib>Yi, Tac-Ghee</creatorcontrib><creatorcontrib>Lim, Hyun-Ja</creatorcontrib><creatorcontrib>Moon, Sun-Hwa</creatorcontrib><creatorcontrib>Lee, Moon-Hee</creatorcontrib><creatorcontrib>Kang, Joon-Soon</creatorcontrib><creatorcontrib>Kim, Chul-Soo</creatorcontrib><creatorcontrib>Lee, Dae-Hyun</creatorcontrib><creatorcontrib>Song, Sun U</creatorcontrib><title>Characterization of mouse clonal mesenchymal stem cell lines established by subfractionation culturing method</title><title>World journal of stem cells</title><addtitle>World Journal of Stem Cells</addtitle><description>AIM:To characterize single-cell-derived mouse clonal mesenchymal stem cells (mcMSCs) established with bone marrow samples from three different mouse strains. METHODS:We established mcMSC lines using subfractionation culturing method from bone marrow samples obtained from long bones.These lines were characterized by measuring cell growth, cell surface epitopes, differentiation potential, lineage-specific gene expression and T-cell suppression capability. Nonclonal MSCs isolated by the conventional gradient centrifugation method were used as controls. RESULTS:All mcMSC lines showed typical nonclonal MSC-like spindle shape morphology. Lines differed inoptimal growth density requirement.Cell surface epitope prof iles of these mcMSC lines were similar to those of nonclonal MSCs. However, some lines exhibited different expression levels in a few epitopes, such as CD44 and CD105. Differentiation assays showed that 90% of the mcMSC lines were capable of differentiating into adipogenic and/or chondrogenic lineages, but only 20% showed osteogenic lineage differentiation. T-cell suppression analysis showed that 75% of the lines exhibited T-cell suppression capability. CONCLUSION:mcMSC lines have similar cell morphology and cell growth rate but exhibit variations in their cell surface epitopes, differentiation potential, lineage-specifi c gene expression and T-cell suppression capability.</description><subject>Bone</subject><subject>cell</subject><subject>cells</subject><subject>Clonal</subject><subject>differentiation</subject><subject>isolation</subject><subject>marrow</subject><subject>Multilineage</subject><subject>Original</subject><subject>stem</subject><subject>stromal</subject><subject>suppression</subject><subject>T-cell</subject><issn>1948-0210</issn><issn>1948-0210</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNpVkU1r3DAQhk1paUKaY69F0ENP3kojWbYvhbKkHxDopT0LSR6vFWQpkewt219fLbsNW100oIdHM_NW1VtGNwIa-Pj7IdvNnm9ct2npi-qa9aKrKTD68qK-qm5zfqDliEZKAa-rKwBKW2jhupq3k07aLpjcH724GEgcyRzXjMT6GLQnM2YMdjrMpc4LzsSi98S7gJlgXrTxLk84EHMgeTXjUVY0J5dd_bImF3bFskxxeFO9GrXPeHu-b6pfX-5-br_V9z--ft9-vq8th4bWWowaBhCt1H3DrJVsaERrpaRSS8laCVZTYSy0yEYUmhnEzsDYcSNMAx2_qT6dvI-rmXGwGJakvXpMbtbpoKJ26v-X4Ca1i3vFWQ8ATRF8OAtSfFrLmGp2-Ti4DliWo7q-Z5xTyQtZn0ibYs4Jx-dfGFXHkNQxJLXnynWqpYV_d9naM_0vkgK8PwunGHZPZXkXRsopB5CS_wVhRZ3r</recordid><startdate>20110826</startdate><enddate>20110826</enddate><creator>Jeon, Myung-Shin</creator><creator>Yi, Tac-Ghee</creator><creator>Lim, Hyun-Ja</creator><creator>Moon, Sun-Hwa</creator><creator>Lee, Moon-Hee</creator><creator>Kang, Joon-Soon</creator><creator>Kim, Chul-Soo</creator><creator>Lee, Dae-Hyun</creator><creator>Song, Sun U</creator><general>Baishideng Publishing Group Co., Limited</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20110826</creationdate><title>Characterization of mouse clonal mesenchymal stem cell lines established by subfractionation culturing method</title><author>Jeon, Myung-Shin ; Yi, Tac-Ghee ; Lim, Hyun-Ja ; Moon, Sun-Hwa ; Lee, Moon-Hee ; Kang, Joon-Soon ; Kim, Chul-Soo ; Lee, Dae-Hyun ; Song, Sun U</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3250-a4fa2d2476a951cc61d547c6606a661762ca04bc27e1fe4a1bee8b2f83b4b5283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Bone</topic><topic>cell</topic><topic>cells</topic><topic>Clonal</topic><topic>differentiation</topic><topic>isolation</topic><topic>marrow</topic><topic>Multilineage</topic><topic>Original</topic><topic>stem</topic><topic>stromal</topic><topic>suppression</topic><topic>T-cell</topic><toplevel>online_resources</toplevel><creatorcontrib>Jeon, Myung-Shin</creatorcontrib><creatorcontrib>Yi, Tac-Ghee</creatorcontrib><creatorcontrib>Lim, Hyun-Ja</creatorcontrib><creatorcontrib>Moon, Sun-Hwa</creatorcontrib><creatorcontrib>Lee, Moon-Hee</creatorcontrib><creatorcontrib>Kang, Joon-Soon</creatorcontrib><creatorcontrib>Kim, Chul-Soo</creatorcontrib><creatorcontrib>Lee, Dae-Hyun</creatorcontrib><creatorcontrib>Song, Sun U</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of stem cells</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jeon, Myung-Shin</au><au>Yi, Tac-Ghee</au><au>Lim, Hyun-Ja</au><au>Moon, Sun-Hwa</au><au>Lee, Moon-Hee</au><au>Kang, Joon-Soon</au><au>Kim, Chul-Soo</au><au>Lee, Dae-Hyun</au><au>Song, Sun U</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of mouse clonal mesenchymal stem cell lines established by subfractionation culturing method</atitle><jtitle>World journal of stem cells</jtitle><addtitle>World Journal of Stem Cells</addtitle><date>2011-08-26</date><risdate>2011</risdate><volume>3</volume><issue>8</issue><spage>70</spage><epage>82</epage><pages>70-82</pages><issn>1948-0210</issn><eissn>1948-0210</eissn><abstract>AIM:To characterize single-cell-derived mouse clonal mesenchymal stem cells (mcMSCs) established with bone marrow samples from three different mouse strains. METHODS:We established mcMSC lines using subfractionation culturing method from bone marrow samples obtained from long bones.These lines were characterized by measuring cell growth, cell surface epitopes, differentiation potential, lineage-specific gene expression and T-cell suppression capability. Nonclonal MSCs isolated by the conventional gradient centrifugation method were used as controls. RESULTS:All mcMSC lines showed typical nonclonal MSC-like spindle shape morphology. Lines differed inoptimal growth density requirement.Cell surface epitope prof iles of these mcMSC lines were similar to those of nonclonal MSCs. However, some lines exhibited different expression levels in a few epitopes, such as CD44 and CD105. Differentiation assays showed that 90% of the mcMSC lines were capable of differentiating into adipogenic and/or chondrogenic lineages, but only 20% showed osteogenic lineage differentiation. T-cell suppression analysis showed that 75% of the lines exhibited T-cell suppression capability. CONCLUSION:mcMSC lines have similar cell morphology and cell growth rate but exhibit variations in their cell surface epitopes, differentiation potential, lineage-specifi c gene expression and T-cell suppression capability.</abstract><cop>United States</cop><pub>Baishideng Publishing Group Co., Limited</pub><pmid>22007272</pmid><doi>10.4252/wjsc.v3.i8.70</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bone cell cells Clonal differentiation isolation marrow Multilineage Original stem stromal suppression T-cell |
title | Characterization of mouse clonal mesenchymal stem cell lines established by subfractionation culturing method |
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