Laser-assisted derivation of human embryonic stem cell lines from IVF embryos after preimplantation genetic diagnosis

被引:42
作者
Turetsky, T. [2 ]
Aizenman, E. [1 ]
Gill, Y. [2 ]
Weinberg, N. [3 ]
Shufaro, Y. [1 ]
Revel, A. [1 ]
Laufer, N. [1 ]
Simon, A. [1 ]
Abeliovich, D. [3 ]
Reubinoff, B. E. [1 ,2 ]
机构
[1] Hadassah Hebrew Univ Med Ctr, Dept Obstet & Gynecol, Jerusalem, Israel
[2] Hadassah Hebrew Univ Med Ctr, Hadassah Human Embryonic Stem Cell Res Ctr, Goldyne Savad Inst Gene Therapy, IL-91120 Jerusalem, Israel
[3] Hadassah Hebrew Univ Med Ctr, Dept Human Genet, IL-91120 Jerusalem, Israel
关键词
laser; preimplantation genetic diagnosis; human embryonic stem cells; derivation; inner cell mass;
D O I
10.1093/humrep/dem351
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: Human embryonic stem cells (hESCs) suitable for future transplantation therapy should preferably be developed in an animal-free system. Our objective was to develop a laser-based system for the isolation of the inner cell mass (ICM) that can develop into hESC lines, thereby circumventing immunosurgery that utilizes animal products. METHODS: Hatching was assisted by micromanipulation techniques through a laser-drilled orifice in the zona pellucida of 13 abnormal preimplantation genetic diagnosed blastocysts. ICMs were dissected from the trophectoderm by a laser beam and plated on feeders to derive hESC lines. RESULTS: eight ICMs were isolated from nine hatched blastocysts and gave rise to three hESC lines affected by myotonic dystrophy type 1, hemophilia A and a carrier of cystic fibrosis 405+ 1G>A mutation. Five blastocysts that collapsed during assisted hatching or ICM dissection were plated whole, giving rise to an additional line affected by fragile X. All cell lines expressed markers of pluripotent stem cells and differentiated in vitro and in vivo into the three germ layers. CONCLUSIONS: These hESC lines can serve as an important model of the genetic disorders that they carry. Laser-assisted isolation of the ICMs may be applied for the derivation of new hESC lines in a xeno-free system for future clinical applications.
引用
收藏
页码:46 / 53
页数:8
相关论文
共 26 条
[1]   Derivation and spontaneous differentiation of human embryonic stem cells [J].
Amit, M ;
Itskovitz-Eldor, J .
JOURNAL OF ANATOMY, 2002, 200 (03) :225-232
[2]   Evaluation of a laser technique to isolate the inner cell mass of murine blastocysts [J].
Cortes, Jose Luis ;
Cobo, Fernando ;
Catalina, Purificacion ;
Nieto, Ana ;
Cabrera, Carmen ;
Montes, Rosa ;
Concha, Angel ;
Menendez, Pablo .
BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, 2007, 46 (205-209) :205-209
[3]  
Cowan CA, 2004, NEW ENGL J MED, V350, P1353, DOI 10.1056/NEJMsr040330
[4]   Derivation of a xeno-free human embryonic stem cell line [J].
Ellerstrom, Catharina ;
Strehl, Raimund ;
Moya, Karina ;
Andersson, Katarina ;
Bergh, Christina ;
Lundin, Kersti ;
Hyllner, Johan ;
Semb, Henrik .
STEM CELLS, 2006, 24 (10) :2170-2176
[5]   Low O2 tensions and the prevention of differentiation of hES cells [J].
Ezashi, T ;
Das, P ;
Roberts, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (13) :4783-4788
[6]  
Gardner DK, 1999, TOWARDS REPRODUCTIVE CERTAINTY, P378
[7]   Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders [J].
Harper, JC ;
Wells, D ;
Piyamongkol, W ;
Abou-Sleiman, P ;
Apessos, A ;
Ioulianos, A ;
Davis, M ;
Doshi, A ;
Serhal, P ;
Ranieri, M ;
Rodeck, C ;
Delhanty, JDA .
PRENATAL DIAGNOSIS, 2002, 22 (06) :525-533
[8]   Derivation, characterization, and differentiation of human embryonic stem cells [J].
Heins, N ;
Englund, MCO ;
Sjöblom, C ;
Dahl, U ;
Tonning, A ;
Bergh, C ;
Lindahl, A ;
Hanson, C ;
Semb, H .
STEM CELLS, 2004, 22 (03) :367-376
[9]   Derivation of human embryonic stem cell lines, towards clinical quality [J].
Hovatta, Outi .
REPRODUCTION FERTILITY AND DEVELOPMENT, 2006, 18 (08) :823-828
[10]   Derivation of neural precursors from human embryonic stem cells in the presence of noggin [J].
Itsykson, P ;
Ilouz, N ;
Turetsky, T ;
Goldstein, RS ;
Pera, MF ;
Fishbein, I ;
Segal, M ;
Reubinoff, BE .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2005, 30 (01) :24-36