Induction of T cell development and establishment of T cell competence from embryonic stem cells differentiated in vitro

被引:268
作者
Schmitt, TM
de Pooter, RF
Gronski, MA
Cho, SK
Ohashi, PS
Zúñiga-Pflücker, JC
机构
[1] Sunnybrook & Womens Coll, Hlth Sci Ctr, Dept Immunol, Toronto, ON M4N 3M5, Canada
[2] Ontario Canc Inst, Dept Med Biophys, Toronto, ON M5G 2M9, Canada
[3] Ontario Canc Inst, Dept Immunol, Toronto, ON M5G 2M9, Canada
基金
加拿大健康研究院;
关键词
D O I
10.1038/ni1055
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Embryonic stem cells (ESCs) have the potential to serve as a renewable source of transplantable tissue-specific stem cells. However, the molecular cues necessary to direct the differentiation of ESCs toward specific cell lineages remain obscure. Here we report the successful induction of ESC differentiation into mature functional T lymphocytes with a simple in vitro coculture system. The directed differentiation of ESCs into T cells required the engagement of Notch receptors by Delta-like 1 ligand (DL1) expressed on the OP9-DL1 stromal cell line. We found a normal program of T cell differentiation in ESC-OP9-DL1 cell cocultures. ESC-derived T cell progenitors effectively reconstituted the T cell compartment of immunodeficient mice, enabling an effective response to a viral infection. These findings provide a powerful tool for the molecular analysis of T cell development and open new avenues for the development of immunotherapeutic approaches using defined sources of stem cells.
引用
收藏
页码:410 / 417
页数:8
相关论文
共 39 条
[1]   Constitutive expression of PU.1 in fetal hematopoietic progenitors blocks T cell development at the pro-T cell stage [J].
Anderson, MK ;
Weiss, AH ;
Hernandez-Hoyos, G ;
Dionne, CJ ;
Rothenberg, EV .
IMMUNITY, 2002, 16 (02) :285-296
[2]   Definition of regulatory network elements for T cell development by perturbation analysis with PU.1 and GATA-3 [J].
Anderson, MK ;
Hernandez-Hoyos, G ;
Dionne, CJ ;
Arias, AM ;
Chen, D ;
Rothenberg, EV .
DEVELOPMENTAL BIOLOGY, 2002, 246 (01) :103-121
[3]   E2A PROTEINS ARE REQUIRED FOR PROPER B-CELL DEVELOPMENT AND INITIATION OF IMMUNOGLOBULIN GENE REARRANGEMENTS [J].
BAIN, G ;
MAANDAG, ECR ;
IZON, DJ ;
AMSEN, D ;
KRUISBEEK, AM ;
WEINTRAUB, BC ;
KROP, I ;
SCHLISSEL, MS ;
FEENEY, AJ ;
VANROON, M ;
VANDERVALK, M ;
TERIELE, HPJ ;
BERNS, A ;
MURRE, C .
CELL, 1994, 79 (05) :885-892
[4]   Functions of E2A-HEB heterodimers in T-cell development revealed by a dominant negative mutation of HEB [J].
Barndt, RJ ;
Dai, MF ;
Zhuang, Y .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (18) :6677-6685
[5]   Requirement for the thymus in αβ T lymphocyte lineage commitment [J].
Carlyle, JR ;
Zúñiga-Pflücker, JC .
IMMUNITY, 1998, 9 (02) :187-197
[6]   Functional characterization of B lymphocytes generated in vitro from embryonic stem cells [J].
Cho, SK ;
Webber, TD ;
Carlyle, JR ;
Nakano, T ;
Lewis, SM ;
Zúñiga-Pflücker, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (17) :9797-9802
[7]  
Cho SK, 2003, METHOD ENZYMOL, V365, P158
[8]   In vitro generation of T lymphocytes from embryonic stem cell-derived prehematopoietic progenitors [J].
de Pooter, RF ;
Cho, SK ;
Carlyle, JR ;
Zúñiga-Pflücker, JC .
BLOOD, 2003, 102 (05) :1649-1653
[9]   Notch1 signaling promotes the maturation of CD4 and CD8 SP thymocytes [J].
Deftos, ML ;
Huang, E ;
Ojala, EW ;
Forbush, KA ;
Bevan, MJ .
IMMUNITY, 2000, 13 (01) :73-84
[10]  
DOETSCHMAN TC, 1985, J EMBRYOL EXP MORPH, V87, P27