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Derivation and characterization of human embryonic stem cell lines from poor quality embryos
Poor quality embryos discarded from in vitro fertilization (IVF) laboratories are good sources for deriving human embryonic stem cell (hESC) lines. In this study, 166 poor quality embryos donated from IVF centers on day 3 were cultured in a blastocyst medium for 2 days, and 32 early blastocysts were...
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Published in: | Journal of genetics and genomics 2009-04, Vol.36 (4), p.229-239 |
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creator | Liu, Weiqiang Yin, Yifei Long, Xiaolin Luo, Yumei Jiang, Yonghua Zhang, Wenhong Du, Hongzi Li, Shaoying Zheng, Yuhong Li, Qing Chen, Xinjie Liao, Baoping Xiao, Guohong Wang, Weihua Sun, Xiaofang |
description | Poor quality embryos discarded from in vitro fertilization (IVF) laboratories are good sources for deriving human embryonic stem cell (hESC) lines. In this study, 166 poor quality embryos donated from IVF centers on day 3 were cultured in a blastocyst medium for 2 days, and 32 early blastocysts were further cultured in a blastocyst optimum culture medium for additional 2 days so that the inner cell masses (ICMs) could be identified and isolated easily. The ICMs of 17 blastocysts were isolated by a mechanical method, while those of the other 15 blastocysts were isolated by immunosurgery. All isolated ICMs were inoculated onto a feeder layer for subcultivation. The rates of ICM attachment, primary ICM colony formation and the efficiency of hESC derivation were similar between the ICMs isolated by the two methods (P〉0.05). As a result, four new hESC lines were established. Three cell lines had normal karyotypes and one had an unbalanced Robertsonian translocation. All cell lines showed normal hESC characteristics and had the differentiation ability. In conclusion, we established a stable and effective method for hESC isolation and culture, and it was confirmed that the mechanical isolation was an effective method to isolate ICMs from poor embryos. These results further indicate that hESC lines can be derived from poor quality embryos discarded by IVF laboratories. |
doi_str_mv | 10.1016/S1673-8527(08)60110-1 |
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In this study, 166 poor quality embryos donated from IVF centers on day 3 were cultured in a blastocyst medium for 2 days, and 32 early blastocysts were further cultured in a blastocyst optimum culture medium for additional 2 days so that the inner cell masses (ICMs) could be identified and isolated easily. The ICMs of 17 blastocysts were isolated by a mechanical method, while those of the other 15 blastocysts were isolated by immunosurgery. All isolated ICMs were inoculated onto a feeder layer for subcultivation. The rates of ICM attachment, primary ICM colony formation and the efficiency of hESC derivation were similar between the ICMs isolated by the two methods (P〉0.05). As a result, four new hESC lines were established. Three cell lines had normal karyotypes and one had an unbalanced Robertsonian translocation. All cell lines showed normal hESC characteristics and had the differentiation ability. In conclusion, we established a stable and effective method for hESC isolation and culture, and it was confirmed that the mechanical isolation was an effective method to isolate ICMs from poor embryos. These results further indicate that hESC lines can be derived from poor quality embryos discarded by IVF laboratories.</description><identifier>ISSN: 1673-8527</identifier><identifier>DOI: 10.1016/S1673-8527(08)60110-1</identifier><identifier>PMID: 19376483</identifier><language>eng</language><publisher>China: Elsevier Ltd</publisher><subject>Blastocyst Inner Cell Mass - cytology ; Cell Culture Techniques - methods ; Cell Differentiation ; Cell Line ; Cell Separation - methods ; Embryo, Mammalian ; embryonic stem cells ; Embryonic Stem Cells - cytology ; Female ; Gene Expression Regulation, Developmental ; Humans ; immunosurgery ; inner cell mass ; Male ; mechanical isolation ; poor quality embryos ; 低质量晶胚 ; 体细胞 ; 免疫力 ; 骨髓干细胞</subject><ispartof>Journal of genetics and genomics, 2009-04, Vol.36 (4), p.229-239</ispartof><rights>2009 Institute of Genetics and Developmental Biology and the Genetics Society of China</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-dc9101184b2d39e9a8d2d72c73c6207816f9c189e1dc5d71330bd812cfaf0b3d3</citedby><cites>FETCH-LOGICAL-c421t-dc9101184b2d39e9a8d2d72c73c6207816f9c189e1dc5d71330bd812cfaf0b3d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/95085X/95085X.jpg</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19376483$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Weiqiang</creatorcontrib><creatorcontrib>Yin, Yifei</creatorcontrib><creatorcontrib>Long, Xiaolin</creatorcontrib><creatorcontrib>Luo, Yumei</creatorcontrib><creatorcontrib>Jiang, Yonghua</creatorcontrib><creatorcontrib>Zhang, Wenhong</creatorcontrib><creatorcontrib>Du, Hongzi</creatorcontrib><creatorcontrib>Li, Shaoying</creatorcontrib><creatorcontrib>Zheng, Yuhong</creatorcontrib><creatorcontrib>Li, Qing</creatorcontrib><creatorcontrib>Chen, Xinjie</creatorcontrib><creatorcontrib>Liao, Baoping</creatorcontrib><creatorcontrib>Xiao, Guohong</creatorcontrib><creatorcontrib>Wang, Weihua</creatorcontrib><creatorcontrib>Sun, Xiaofang</creatorcontrib><title>Derivation and characterization of human embryonic stem cell lines from poor quality embryos</title><title>Journal of genetics and genomics</title><addtitle>Journal of Genetics and Genomics</addtitle><description>Poor quality embryos discarded from in vitro fertilization (IVF) laboratories are good sources for deriving human embryonic stem cell (hESC) lines. In this study, 166 poor quality embryos donated from IVF centers on day 3 were cultured in a blastocyst medium for 2 days, and 32 early blastocysts were further cultured in a blastocyst optimum culture medium for additional 2 days so that the inner cell masses (ICMs) could be identified and isolated easily. The ICMs of 17 blastocysts were isolated by a mechanical method, while those of the other 15 blastocysts were isolated by immunosurgery. All isolated ICMs were inoculated onto a feeder layer for subcultivation. The rates of ICM attachment, primary ICM colony formation and the efficiency of hESC derivation were similar between the ICMs isolated by the two methods (P〉0.05). As a result, four new hESC lines were established. Three cell lines had normal karyotypes and one had an unbalanced Robertsonian translocation. All cell lines showed normal hESC characteristics and had the differentiation ability. In conclusion, we established a stable and effective method for hESC isolation and culture, and it was confirmed that the mechanical isolation was an effective method to isolate ICMs from poor embryos. These results further indicate that hESC lines can be derived from poor quality embryos discarded by IVF laboratories.</description><subject>Blastocyst Inner Cell Mass - cytology</subject><subject>Cell Culture Techniques - methods</subject><subject>Cell Differentiation</subject><subject>Cell Line</subject><subject>Cell Separation - methods</subject><subject>Embryo, Mammalian</subject><subject>embryonic stem cells</subject><subject>Embryonic Stem Cells - cytology</subject><subject>Female</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Humans</subject><subject>immunosurgery</subject><subject>inner cell mass</subject><subject>Male</subject><subject>mechanical isolation</subject><subject>poor quality embryos</subject><subject>低质量晶胚</subject><subject>体细胞</subject><subject>免疫力</subject><subject>骨髓干细胞</subject><issn>1673-8527</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkE1v1DAQhn0A0artTwBZHBAcAh47648TQgUKUiUOwA3JcuxJ1yKxd-2k0vLryXYjOPZk6dXzemYeQp4DewsM5LvvIJVo9Iar10y_kQyANfCEnP-Lz8hVrbFjjDNhlFLPyBkYoWSrxTn59RFLvHdTzIm6FKjfuuL8tIR_TmHu6XYeXaI4duWQU_S0TjhSj8NAh5iw0r7kke5yLnQ_uyFOh5Wtl-Rp74aKV-t7QX5-_vTj-ktz--3m6_WH28a3HKYmeLNcArrteBAGjdOBB8W9El5ypjTI3njQBiH4TVAgBOuCBu5717NOBHFBXp3-3ZW8n7FOdoz1uKBLmOdq5dJR3PBHQc5k23LRLuDmBPqSay3Y212JoysHC8wetdsH7fbo1zJtH7RbWHov1gFzN2L431qFL8D7E4CLj_uIxVYfMXkMsaCfbMjx0REv19W2Od3tY7qznfO_-zigFYwZZjZS_AXLhaAc</recordid><startdate>20090401</startdate><enddate>20090401</enddate><creator>Liu, Weiqiang</creator><creator>Yin, Yifei</creator><creator>Long, Xiaolin</creator><creator>Luo, Yumei</creator><creator>Jiang, Yonghua</creator><creator>Zhang, Wenhong</creator><creator>Du, Hongzi</creator><creator>Li, Shaoying</creator><creator>Zheng, Yuhong</creator><creator>Li, Qing</creator><creator>Chen, Xinjie</creator><creator>Liao, Baoping</creator><creator>Xiao, Guohong</creator><creator>Wang, Weihua</creator><creator>Sun, Xiaofang</creator><general>Elsevier Ltd</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W94</scope><scope>WU4</scope><scope>~WA</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20090401</creationdate><title>Derivation and characterization of human embryonic stem cell lines from poor quality embryos</title><author>Liu, Weiqiang ; Yin, Yifei ; Long, Xiaolin ; Luo, Yumei ; Jiang, Yonghua ; Zhang, Wenhong ; Du, Hongzi ; Li, Shaoying ; Zheng, Yuhong ; Li, Qing ; Chen, Xinjie ; Liao, Baoping ; Xiao, Guohong ; Wang, Weihua ; Sun, Xiaofang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-dc9101184b2d39e9a8d2d72c73c6207816f9c189e1dc5d71330bd812cfaf0b3d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Blastocyst Inner Cell Mass - cytology</topic><topic>Cell Culture Techniques - methods</topic><topic>Cell Differentiation</topic><topic>Cell Line</topic><topic>Cell Separation - methods</topic><topic>Embryo, Mammalian</topic><topic>embryonic stem cells</topic><topic>Embryonic Stem Cells - cytology</topic><topic>Female</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Humans</topic><topic>immunosurgery</topic><topic>inner cell mass</topic><topic>Male</topic><topic>mechanical isolation</topic><topic>poor quality embryos</topic><topic>低质量晶胚</topic><topic>体细胞</topic><topic>免疫力</topic><topic>骨髓干细胞</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Weiqiang</creatorcontrib><creatorcontrib>Yin, Yifei</creatorcontrib><creatorcontrib>Long, Xiaolin</creatorcontrib><creatorcontrib>Luo, Yumei</creatorcontrib><creatorcontrib>Jiang, Yonghua</creatorcontrib><creatorcontrib>Zhang, Wenhong</creatorcontrib><creatorcontrib>Du, Hongzi</creatorcontrib><creatorcontrib>Li, Shaoying</creatorcontrib><creatorcontrib>Zheng, Yuhong</creatorcontrib><creatorcontrib>Li, Qing</creatorcontrib><creatorcontrib>Chen, Xinjie</creatorcontrib><creatorcontrib>Liao, Baoping</creatorcontrib><creatorcontrib>Xiao, Guohong</creatorcontrib><creatorcontrib>Wang, Weihua</creatorcontrib><creatorcontrib>Sun, Xiaofang</creatorcontrib><collection>维普_期刊</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-自然科学</collection><collection>中文科技期刊数据库-自然科学-生物科学</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of genetics and genomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Weiqiang</au><au>Yin, Yifei</au><au>Long, Xiaolin</au><au>Luo, Yumei</au><au>Jiang, Yonghua</au><au>Zhang, Wenhong</au><au>Du, Hongzi</au><au>Li, Shaoying</au><au>Zheng, Yuhong</au><au>Li, Qing</au><au>Chen, Xinjie</au><au>Liao, Baoping</au><au>Xiao, Guohong</au><au>Wang, Weihua</au><au>Sun, Xiaofang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Derivation and characterization of human embryonic stem cell lines from poor quality embryos</atitle><jtitle>Journal of genetics and genomics</jtitle><addtitle>Journal of Genetics and Genomics</addtitle><date>2009-04-01</date><risdate>2009</risdate><volume>36</volume><issue>4</issue><spage>229</spage><epage>239</epage><pages>229-239</pages><issn>1673-8527</issn><abstract>Poor quality embryos discarded from in vitro fertilization (IVF) laboratories are good sources for deriving human embryonic stem cell (hESC) lines. In this study, 166 poor quality embryos donated from IVF centers on day 3 were cultured in a blastocyst medium for 2 days, and 32 early blastocysts were further cultured in a blastocyst optimum culture medium for additional 2 days so that the inner cell masses (ICMs) could be identified and isolated easily. The ICMs of 17 blastocysts were isolated by a mechanical method, while those of the other 15 blastocysts were isolated by immunosurgery. All isolated ICMs were inoculated onto a feeder layer for subcultivation. The rates of ICM attachment, primary ICM colony formation and the efficiency of hESC derivation were similar between the ICMs isolated by the two methods (P〉0.05). As a result, four new hESC lines were established. Three cell lines had normal karyotypes and one had an unbalanced Robertsonian translocation. All cell lines showed normal hESC characteristics and had the differentiation ability. In conclusion, we established a stable and effective method for hESC isolation and culture, and it was confirmed that the mechanical isolation was an effective method to isolate ICMs from poor embryos. These results further indicate that hESC lines can be derived from poor quality embryos discarded by IVF laboratories.</abstract><cop>China</cop><pub>Elsevier Ltd</pub><pmid>19376483</pmid><doi>10.1016/S1673-8527(08)60110-1</doi><tpages>11</tpages></addata></record> |
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subjects | Blastocyst Inner Cell Mass - cytology Cell Culture Techniques - methods Cell Differentiation Cell Line Cell Separation - methods Embryo, Mammalian embryonic stem cells Embryonic Stem Cells - cytology Female Gene Expression Regulation, Developmental Humans immunosurgery inner cell mass Male mechanical isolation poor quality embryos 低质量晶胚 体细胞 免疫力 骨髓干细胞 |
title | Derivation and characterization of human embryonic stem cell lines from poor quality embryos |
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