Derivation of human embryonic stem cell lines from embryos obtained after IVF and after PGD for monogenic disorders

被引:166
作者
Mateizel, I
De Temmerman, N
Ullmann, U
Cauffman, G
Sermon, K
Van de Velde, H
De Rycke, M
Degreef, E
Devroey, P
Liebaers, I
Van Steirteghem, A
机构
[1] Free Univ Brussels, Dutch Speaking Brussels Free Univ, Univ Hosp, Res Ctr Reprod & Genet, B-1090 Brussels, Belgium
[2] Free Univ Brussels, Dutch Speaking Brussels Free Univ, Ctr Genet Med, B-1090 Brussels, Belgium
[3] Free Univ Brussels, Dutch Speaking Brussels Free Univ, Ctr Reprod Med, B-1090 Brussels, Belgium
[4] Free Univ Brussels, Dutch Speaking Brussels Free Univ, Univ Hosp, Dept Pathol, B-1090 Brussels, Belgium
[5] Free Univ Brussels, Dutch Speaking Brussels Free Univ, Sch Med, B-1090 Brussels, Belgium
关键词
cystic fibrosis; disease models; human embryonic stem cells; Huntington disease; myotonic dystrophy;
D O I
10.1093/humrep/dei345
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: Human embryonic stem (hES) cells are pluripotent cells usually derived from the inner cell mass (ICM) of blastocysts. Because of their ability to differentiate into all three embryonic germ layers, hES cells represent an important material for studying developmental biology and cell replacement therapy. hES cell lines derived from blastocysts diagnosed as carrying a genetic disorder after PGD represent in vitro disease models. METHODS: ICMs isolated by immunosurgery from human blastocysts donated for research after IVF cycles and after PGD were plated in serum-free medium (except VUB01) on mouse feeder layers. RESULTS: Five hES cell lines were isolated, two from IVF embryos and three from PGD embryos. All lines behave similarly in culture and present a normal karyotype. The lines express all the markers considered characteristic of undifferentiated hES cells and were proven to be pluripotent both in vitro and in vivo (ongoing for VUB05_HD). CONCLUSIONS: We report here on the derivation of two hES cell lines presumed to be genetically normal (VUB01 and VUB02) and three hES cell lines carrying mutations for myotonic dystrophy type 1 (VUB03_DM1), cystic fibrosis (VUB04_CF) and Huntington disease (VUB05_HD).
引用
收藏
页码:503 / 511
页数:9
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