Generation of pluripotent stem cells from neonatal mouse testis

被引:774
作者
Kanatsu-Shinohara, M
Inoue, K
Lee, J
Yoshimoto, M
Ogonuki, N
Miki, H
Baba, S
Kato, T
Kazuki, Y
Toyokuni, S
Toyoshima, M
Niwa, O
Oshimura, M
Heike, T
Nakahata, T
Ishino, F
Ogura, A
Shinohara, T [1 ]
机构
[1] Kyoto Univ, Horizontal Med Res Org, Kyoto 6068501, Japan
[2] Kyoto Univ, Dept Pathol & Biol Dis, Grad Sch Med, Kyoto 6068501, Japan
[3] Kyoto Univ, Ctr Radiat Biol, Kyoto 6068501, Japan
[4] Kyoto Univ, Grad Sch Med, Dept Pediat, Kyoto 6068507, Japan
[5] RIKEN, Bioresource Ctr, Inst Phys & Chem Res, Ibaraki 3050074, Japan
[6] Tokyo Med & Dent Univ, Med Res Inst, Tokyo 1010062, Japan
[7] Tottori Univ, Fac Med, Sch Life Sci, Dept Mol & Cell Genet, Tottori 6838503, Japan
关键词
D O I
10.1016/j.cell.2004.11.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Although germline cells can form multipotential embryonic stem (ES)/embryonic germ (EG) cells, these cells can be derived only from embryonic tissues, and such multipotent cells have not been available from neonatal gonads. Here we report the successful establishment of ES-like cells from neonatal mouse testis. These ES-like cells were phenotypically similar to ES/ EG cells except in their genomic imprinting pattern. They differentiated into various types of somatic cells in vitro under conditions used to induce the differentiation of ES cells and produced teratomas after inoculation into mice. Furthermore, these ES-like cells formed germline chimeras when injected into blastocysts. Thus, the capacity to form multipotent cells persists in neonatal testis. The ability to derive multipotential stem cells from the neonatal testis has important implications for germ cell biology and opens the possibility of using these cells for biotechnology and medicine.
引用
收藏
页码:1001 / 1012
页数:12
相关论文
共 56 条
[1]
Comprehensive transcriptome analysis of differentiation of embryonic stem cells into midbrain and hindbrain neurons [J].
Ahn, JI ;
Lee, KH ;
Shin, DM ;
Shim, JW ;
Lee, JS ;
Chang, SY ;
Lee, YS ;
Brownstein, MJ ;
Lee, SH ;
Lee, YS .
DEVELOPMENTAL BIOLOGY, 2004, 265 (02) :491-501
[2]
Anderson R, 1999, J REPROD FERTIL, V116, P379, DOI 10.1530/jrf.0.1160379
[3]
SPERMATOGENESIS FOLLOWING MALE GERM-CELL TRANSPLANTATION [J].
BRINSTER, RL ;
ZIMMERMANN, JW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (24) :11298-11302
[4]
GERMLINE TRANSMISSION OF DONOR HAPLOTYPE FOLLOWING SPERMATOGONIAL TRANSPLANTATION [J].
BRINSTER, RL ;
AVARBOCK, MR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (24) :11303-11307
[5]
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
[6]
The H19 methylation imprint is erased and re-established differentially on the parental alleles during male germ cell development [J].
Davis, TL ;
Yang, GJ ;
McCarrey, JR ;
Bartolomei, MS .
HUMAN MOLECULAR GENETICS, 2000, 9 (19) :2885-2894
[7]
Acquisition of the H19 methylation imprint occurs differentially on the parental alleles during spermatogenesis [J].
Davis, TL ;
Trasler, JM ;
Moss, SB ;
Yang, GJ ;
Bartolomei, MS .
GENOMICS, 1999, 58 (01) :18-28
[8]
De Rooij DG, 2000, J ANDROL, V21, P776
[9]
Dean W, 1998, DEVELOPMENT, V125, P2273
[10]
ESTABLISHMENT IN CULTURE OF PLURIPOTENTIAL CELLS FROM MOUSE EMBRYOS [J].
EVANS, MJ ;
KAUFMAN, MH .
NATURE, 1981, 292 (5819) :154-156