Physiologic oxygen enhances human embryonic stem cell clonal recovery and reduces chromosomal abnormalities

被引:144
作者
Forsyth, NR [1 ]
Musio, A
Vezzoni, P
Simpson, AHRW
Noble, BS
McWhir, J
机构
[1] Roslin Inst, Roslin EH25 9PS, Midlothian, Scotland
[2] CNR, Ist Tecnol Biomed, I-20133 Milan, Italy
[3] Univ Edinburgh, Sch Med, Musculoskeletal Res Unit, Edinburgh, Midlothian, Scotland
基金
英国医学研究理事会;
关键词
D O I
10.1089/clo.2006.8.16
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Human embryonic stem cells (hESC) have great potential in regenerative medicine, provided that culture systems are established that maintain genomic integrity. Here we describe a comparison of the effects of culture in either physiologic oxygen (2%) or room oxygen (21%) on the hESC lines, H1, H9, and RH1. Physiologic oxygen enabled an average sixfold increase in clone recovery across the hESC lines tested (p < 0.001). FACS analysis showed that cells cultured in physiologic oxygen were significantly smaller and less granular. No significant changes had occurred in levels of SSEA4, SSEA1, TRA-1-60, or TRA-1-81. While karyotypic normalcy was maintained in both H1 and H9, the frequency of spontaneous chromosomal aberrations was significantly increased in room oxygen. This increase was not observed in physiologic oxygen. These results clearly demonstrate that physiologic oxygen culture conditions are indispensable for robust hES clone recovery and may enhance the isolation of novel hES lines and transgenic clones.
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页码:16 / 23
页数:8
相关论文
共 23 条
[1]  
Adam AAG, 2004, JPN J VET RES, V52, P77
[2]   Clonally derived human embryonic stem cell lines maintain pluripotency and proliferative potential for prolonged periods of culture [J].
Amit, M ;
Carpenter, MK ;
Inokuma, MS ;
Chiu, CP ;
Harris, CP ;
Waknitz, MA ;
Itskovitz-Eldor, J ;
Thomson, JA .
DEVELOPMENTAL BIOLOGY, 2000, 227 (02) :271-278
[3]  
Badcock G, 1999, CANCER RES, V59, P4715
[4]   Oxygen accelerates the accumulation of mutations during the senescence and immortalization of murine cells in culture [J].
Busuttil, RA ;
Rubio, M ;
Dollé, MET ;
Campisi, J ;
Vijg, J .
AGING CELL, 2003, 2 (06) :287-294
[5]   Recurrent gain of chromosomes 17q and 12 in cultured human embryonic stem cells [J].
Draper, JS ;
Smith, K ;
Gokhale, P ;
Moore, HD ;
Maltby, E ;
Johnson, J ;
Meisner, L ;
Zwaka, TP ;
Thomson, JA ;
Andrews, PW .
NATURE BIOTECHNOLOGY, 2004, 22 (01) :53-54
[6]   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
[7]  
FISCHER B, 1993, J REPROD FERTIL, V99, P673, DOI 10.1530/jrf.0.0990673
[8]   Developmental differences in the immortalization of lung fibroblasts by telomerase [J].
Forsyth, NR ;
Evans, AP ;
Shay, JW ;
Wright, WE .
AGING CELL, 2003, 2 (05) :235-243
[9]   The promise of human embryonic stem cells [J].
Gerecht-Nir, S ;
Itskovitz-Eldor, J .
BEST PRACTICE & RESEARCH CLINICAL OBSTETRICS & GYNAECOLOGY, 2004, 18 (06) :843-852
[10]   THE EFFECT OF OXYGEN-TENSION ON COLONY FORMATION AND CELL-PROLIFERATION OF AMNIOTIC-FLUID CELLS-INVITRO [J].
HELD, KR ;
SONNICHSEN, S .
PRENATAL DIAGNOSIS, 1984, 4 (03) :171-179