Establishment of Rat Embryonic Stem Cells and Making of Chimera Rats

被引:51
作者
Ueda, Shinobu [1 ,2 ]
Kawamata, Masaki [1 ]
Teratani, Takumi [1 ]
Shimizu, Taku [3 ]
Tamai, Yoshitaka [3 ]
Ogawa, Hiromasa [4 ]
Hayashi, Katsuyuki [5 ]
Tsuda, Hiroyuki [6 ]
Ochiya, Takahiro [1 ]
机构
[1] Natl Canc Ctr, Res Inst, Sect Studies Metastasis, Tokyo 104, Japan
[2] Waseda Univ, Comprehensive Res Org, Tokyo, Japan
[3] BANYU, Tsukuba Res Inst, Tsukuba, Ibaraki, Japan
[4] CLEA Japan Inc, Tokyo, Japan
[5] DNA Chip Res Inc, Yokohama, Kanagawa, Japan
[6] Nagoya City Univ, Grad Sch Med Sci, Dept Mol Toxicol, Nagoya, Aichi, Japan
来源
PLOS ONE | 2008年 / 3卷 / 07期
关键词
D O I
10.1371/journal.pone.0002800
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The rat is a reference animal model for physiological studies and for the analysis of multigenic human diseases such as hypertension, diabetes, neurological disorders, and cancer. The rats have long been used in extensive chemical carcinogenesis studies. Thus, the rat embryonic stem (rES) cell is an important resource for the study of disease models. Attempts to derive ES cells from various mammals, including the rat, have not succeeded. Here we have established two independent rES cells from Wister rat blastocysts that have undifferentiated characters such as Nanog and Oct3/4 genes expression and they have stage-specific embryonic antigen (SSEA) -1, -3, -4, and TRA-1-81 expression. The cells were successfully cultured in an undifferentiated state and can be possible over 18 passages with maintaining more than 40% of normal karyotype. Their pluripotent potential was confirmed by the differentiation into derivatives of the endoderm, mesoderm, and ectoderm. Most importantly, the rES cells are capable of producing chimera rats. Therefore, we established pluripotent rES cell lines that are widely used to produce genetically modified experimental rats for study of human diseases.
引用
收藏
页数:9
相关论文
共 34 条
[1]   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
[2]   Core transcriptional regulatory circuitry in human embryonic stem cells [J].
Boyer, LA ;
Lee, TI ;
Cole, MF ;
Johnstone, SE ;
Levine, SS ;
Zucker, JR ;
Guenther, MG ;
Kumar, RM ;
Murray, HL ;
Jenner, RG ;
Gifford, DK ;
Melton, DA ;
Jaenisch, R ;
Young, RA .
CELL, 2005, 122 (06) :947-956
[3]   FORMATION OF GERM-LINE CHIMERAS FROM EMBRYO-DERIVED TERATOCARCINOMA CELL-LINES [J].
BRADLEY, A ;
EVANS, M ;
KAUFMAN, MH ;
ROBERTSON, E .
NATURE, 1984, 309 (5965) :255-256
[4]   Rat embryonic stem cells: A progress report [J].
Brenin, D ;
Look, J ;
Bader, M ;
Hubner, N ;
Levan, G ;
Iannaccone, P .
TRANSPLANTATION PROCEEDINGS, 1997, 29 (03) :1761-1765
[5]   Karyotypic stability, genotyping, differentiation, feeder-free maintenance, and gene expression sampling in three human embryonic stem cell lines derived prior to August 9, 2001 [J].
Brimble, SN ;
Zeng, XM ;
Weiler, DA ;
Luo, YQ ;
Liu, Y ;
Lyons, IG ;
Freed, WJ ;
Robins, AJ ;
Rao, MS ;
Schulz, TC .
STEM CELLS AND DEVELOPMENT, 2004, 13 (06) :585-597
[6]   Derivation of pluripotent epiblast stem cells from mammalian embryos [J].
Brons, I. Gabrielle M. ;
Smithers, Lucy E. ;
Trotter, Matthew W. B. ;
Rugg-Gunn, Peter ;
Sun, Bowen ;
de Sousa Lopes, Susana M. Chuva ;
Howlett, Sarah K. ;
Clarkson, Amanda ;
Ahrlund-Richter, Lars ;
Pedersen, Roger A. ;
Vallier, Ludovic .
NATURE, 2007, 448 (7150) :191-U7
[7]   Functional expression cloning of Nanog, a pluripotency sustaining factor in embryonic stem cells [J].
Chambers, I ;
Colby, D ;
Robertson, M ;
Nichols, J ;
Lee, S ;
Tweedie, S ;
Smith, A .
CELL, 2003, 113 (05) :643-655
[8]   ISOLATION OF MOUSE PRIMORDIAL GERM-CELLS [J].
DEFELICI, M ;
MCLAREN, A .
EXPERIMENTAL CELL RESEARCH, 1982, 142 (02) :476-482
[9]   ESTABLISHMENT IN CULTURE OF PLURIPOTENTIAL CELLS FROM MOUSE EMBRYOS [J].
EVANS, MJ ;
KAUFMAN, MH .
NATURE, 1981, 292 (5819) :154-156
[10]   ISOLATION OF A DEAD-FAMILY PROTEIN GENE THAT ENCODES A MURINE HOMOLOG OF DROSOPHILA-VASA AND ITS SPECIFIC EXPRESSION IN GERM-CELL LINEAGE [J].
FUJIWARA, Y ;
KOMIYA, T ;
KAWABATA, H ;
SATO, M ;
FUJIMOTO, H ;
FURUSAWA, M ;
NOCE, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (25) :12258-12262