T lineage differentiation from human embryonic stem cells

被引:101
|
作者
Galic, Zoran
Kitchen, Scott G.
Kacena, Amelia
Subramanian, Aparna
Burke, Bryan
Cortado, Ruth
Zack, Jerome A.
机构
[1] Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, AIDS Inst, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Inst Stem Cell Biol & Med, Los Angeles, CA 90095 USA
关键词
SCID-hu mouse; T cell development; gene therapy; immune reconstitution; hematopoiesis;
D O I
10.1073/pnas.0604244103
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
Harnessing the ability of genetically manipulated human embryonic stem cells (hESC) to differentiate into appropriate lineages could revolutionize medical practice. These cells have the theoretical potential to develop into all mature cell types; however, the actual ability to develop into all hematopoietic lineages has not been demonstrated. Using sequential in vitro coculture on murine bone marrow stromal cells, and engraftment into human thymic tissues in immunodeficient mice, we demonstrate that hESC can differentiate through the T lymphoid lineage. Stable transgene expression was maintained at high levels throughout differentiation, suggesting that genetically manipulated hESC hold potential to treat several T cell disorders.
引用
收藏
页码:11742 / 11747
页数:6
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