Human embryonic stem cells have enhanced repair of multiple forms of DNA damage
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Human embryonic stem cells have enhanced repair of multiple forms of DNA damage. / Maynard, Scott; Swistowska, Anna Maria; Lee, Jae Wan; Liu, Ying; Liu, Su-Ting; Da Cruz, Alexandre Bettencourt; Rao, Mahendra; de Souza-Pinto, Nadja C; Zeng, Xianmin; Bohr, Vilhelm A.
In: Stem Cells, Vol. 26, No. 9, 01.09.2008, p. 2266-74.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Human embryonic stem cells have enhanced repair of multiple forms of DNA damage
AU - Maynard, Scott
AU - Swistowska, Anna Maria
AU - Lee, Jae Wan
AU - Liu, Ying
AU - Liu, Su-Ting
AU - Da Cruz, Alexandre Bettencourt
AU - Rao, Mahendra
AU - de Souza-Pinto, Nadja C
AU - Zeng, Xianmin
AU - Bohr, Vilhelm A
PY - 2008/9/1
Y1 - 2008/9/1
N2 - Embryonic stem cells need to maintain genomic integrity so that they can retain the ability to differentiate into multiple cell types without propagating DNA errors. Previous studies have suggested that mechanisms of genome surveillance, including DNA repair, are superior in mouse embryonic stem cells compared with various differentiated murine cells. Using single-cell gel electrophoresis (comet assay) we found that human embryonic stem cells (BG01, I6) have more efficient repair of different types of DNA damage (generated from H2O2, UV-C, ionizing radiation, or psoralen) than human primary fibroblasts (WI-38, hs27) and, with the exception of UV-C damage, HeLa cells. Microarray gene expression analysis showed that mRNA levels of several DNA repair genes are elevated in human embryonic stem cells compared with their differentiated forms (embryoid bodies). These data suggest that genomic maintenance pathways are enhanced in human embryonic stem cells, relative to differentiated human cells.
AB - Embryonic stem cells need to maintain genomic integrity so that they can retain the ability to differentiate into multiple cell types without propagating DNA errors. Previous studies have suggested that mechanisms of genome surveillance, including DNA repair, are superior in mouse embryonic stem cells compared with various differentiated murine cells. Using single-cell gel electrophoresis (comet assay) we found that human embryonic stem cells (BG01, I6) have more efficient repair of different types of DNA damage (generated from H2O2, UV-C, ionizing radiation, or psoralen) than human primary fibroblasts (WI-38, hs27) and, with the exception of UV-C damage, HeLa cells. Microarray gene expression analysis showed that mRNA levels of several DNA repair genes are elevated in human embryonic stem cells compared with their differentiated forms (embryoid bodies). These data suggest that genomic maintenance pathways are enhanced in human embryonic stem cells, relative to differentiated human cells.
KW - Cell Differentiation
KW - Comet Assay
KW - DNA Damage
KW - DNA Repair
KW - Embryonic Stem Cells
KW - Fibroblasts
KW - Ficusin
KW - Hela Cells
KW - Humans
KW - Hydrogen Peroxide
KW - Oligonucleotide Array Sequence Analysis
KW - Radiation, Ionizing
KW - Ultraviolet Rays
U2 - 10.1634/stemcells.2007-1041
DO - 10.1634/stemcells.2007-1041
M3 - Journal article
C2 - 18566332
VL - 26
SP - 2266
EP - 2274
JO - Stem Cells
JF - Stem Cells
SN - 1066-5099
IS - 9
ER -
ID: 33566563