Parp1-deficiency induces differentiation of ES cells into trophoblast derivatives

被引:71
作者
Hemberger, M
Nozaki, T
Winterhager, E
Yamamoto, H
Nakagama, H
Kamada, N
Suzuki, H
Ohta, T
Ohki, M
Masutani, M
Cross, JC
机构
[1] Univ Calgary, Dept Biochem & Mol Biol, Calgary, AB T2N 4N1, Canada
[2] Natl Canc Ctr, Div Biochem, Inst Res, Chuo Ku, Tokyo 1040045, Japan
[3] Univ Essen Gesamthsch, Inst Anat, Essen, Germany
[4] Chugai Pharmaceut Co Ltd, Pharmaceut Technol Lab, Shizuoka 4128513, Japan
[5] Natl Canc Ctr, Med Genom Ctr, Chuo Ku, Tokyo 1040045, Japan
基金
加拿大健康研究院;
关键词
D O I
10.1016/S0012-1606(03)00097-6
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Embryonic stem (ES) cells deficient in the enzyme poly(ADP-ribose) polymerase (Parp1) develop into teratocarcinoma-like tumors when injected subcutaneously into nude mice that contain cells with giant cell-like morphology. We show here that these cells express genes characteristic of trophoblast giant cells and thus belong to the trophectoderm. lineage. In addition, Parp1(-/-) tumors contained other trophoblast subtypes as revealed by expression of spongiotrophoblast-specific marker genes. The extent of giant cell differentiation was enhanced, however, as compared with spongiotrophoblast. A similar shift toward trophoblast giant cell differentiation was observed in cultures of Parp1-deficient ES cells and in placentae of Parp1(-/-) embryos. Analysis of other cell lineage markers demonstrated that Parp1 acts exclusively in trophoblast to suppress differentiation. Surprisingly, trophoblast derivatives were also detected in wildtype tumors and cultured ES cells, albeit at significantly lower frequency. These data show that wildtype ES cells contain a small population of cells with trophectoderm potential and that absence of Parp1 renders ES cells more susceptible to adopting a trophoblast phenotype. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:371 / 381
页数:11
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