Pluripotency of spermatogonial stem cells from adult mouse testis

被引:629
作者
Guan, K
Nayernia, K
Maier, LS
Wagner, S
Dressel, R
Lee, JH
Nolte, J
Wolf, F
Li, MY
Engel, W
Hasenfuss, G
机构
[1] Univ Gottingen, Ctr Heart, Dept Cardiol & Pneumol, D-37075 Gottingen, Germany
[2] Univ Gottingen, Inst Human Genet, D-37073 Gottingen, Germany
[3] Univ Gottingen, Dept Cellular & Mol Immunol, D-37073 Gottingen, Germany
关键词
D O I
10.1038/nature04697
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
Embryonic germ cells as well as germline stem cells from neonatal mouse testis are pluripotent and have differentiation potential similar to embryonic stem cells(1,2), suggesting that the germline lineage may retain the ability to generate pluripotent cells. However, until now there has been no evidence for the pluripotency and plasticity of adult spermatogonial stem cells (SSCs), which are responsible for maintaining spermatogenesis throughout life in the male(3). Here we show the isolation of SSCs from adult mouse testis using genetic selection, with a success rate of 27%. These isolated SSCs respond to culture conditions and acquire embryonic stem cell properties. We name these cells multipotent adult germline stem cells (maGSCs). They are able to spontaneously differentiate into derivatives of the three embryonic germ layers in vitro and generate teratomas in immunodeficient mice. When injected into an early blastocyst, SSCs contribute to the development of various organs and show germline transmission. Thus, the capacity to form multipotent cells persists in adult mouse testis. Establishment of human maGSCs from testicular biopsies may allow individual cell-based therapy without the ethical and immunological problems associated with human embryonic stem cells. Furthermore, these cells may provide new opportunities to study genetic diseases in various cell lineages.
引用
收藏
页码:1199 / 1203
页数:5
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