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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
Main Authors: 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
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cited_by cdi_FETCH-LOGICAL-c421t-dc9101184b2d39e9a8d2d72c73c6207816f9c189e1dc5d71330bd812cfaf0b3d3
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creator Liu, Weiqiang
Yin, Yifei
Long, Xiaolin
Luo, Yumei
Jiang, Yonghua
Zhang, Wenhong
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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. 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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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