WNT/β-catenin pathway up-regulates Stat3 and converges on LIF to prevent differentiation of mouse embryonic stem cells

被引:237
作者
Hao, J [1 ]
Li, TG [1 ]
Qi, XX [1 ]
Zhao, DF [1 ]
Zhao, GQ [1 ]
机构
[1] Univ Texas, SW Med Ctr, Cecil H & Ida Green Ctr Reprod Biol Sci, Dept Pharmacol, Dallas, TX 75390 USA
关键词
embryonic stem cells; growth factors; pluripotency; mouse; WNT/beta-catenin; STAT3;
D O I
10.1016/j.ydbio.2005.11.011
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Embryonic stem (ES) cells rely oil growth factors provided by feeder cells or exogenously to maintain their pluripotency. In order to identify such factors, we have established sub-lines of STO feeder cells which exhibit variable ability in supporting ES cell self-renewal. Functional screening identifies WNT5A and WNT6 as STO cell-produced factors that potently inhibit ES cell differentiation in a serum-dependent manner. Furthermore, direct activation of beta-catenin without disturbing the upstream components of the WNT/beta-catenin pathway fully recapitulates the effect of WNTs on ES cells. Importantly, the WNT/beta-catenin pathway up-regulates the mRNA for Stat3, a known regulator of ES cell self-renewal in the mouse. Finally, LIF is able to mimic the serum effect to act synergistically with WNT proteins to inhibit ES cell differentiation. Therefore, our study reveals part of the molecular mechanisms by which the WNT/beta-catenin pathway acts to prevent ES cell differentiation through convergence on the LIF/JAK-STAT pathway at the level of STAT3. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:81 / 91
页数:11
相关论文
共 50 条
[1]  
[Anonymous], 1994, MANIPULATING MOUSE E
[2]  
[Anonymous], PROGR ASIAN SOCIAL P
[3]   Brachyury is a target gene of the Wnt/β-catenin signaling pathway [J].
Arnold, SJ ;
Stappert, J ;
Bauer, A ;
Kispert, A ;
Herrmann, BG ;
Kemler, R .
MECHANISMS OF DEVELOPMENT, 2000, 91 (1-2) :249-258
[4]   A role for the Wnt gene family in hematopoiesis: Expansion of multilineage progenitor cells [J].
Austin, TW ;
Solar, GP ;
Ziegler, FC ;
Liem, L ;
Matthews, W .
BLOOD, 1997, 89 (10) :3624-3635
[5]  
Barker N, 2000, ADV CANCER RES, V77, P1
[6]   The Wnt/β-catenin→Pitx2 pathway controls the turnover of Pitx2 and other unstable mRNAs [J].
Briata, P ;
Ilengo, C ;
Corte, G ;
Moroni, C ;
Rosenfeld, MG ;
Chen, CY ;
Gherzi, R .
MOLECULAR CELL, 2003, 12 (05) :1201-1211
[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]   ESTABLISHMENT IN CULTURE OF PLURIPOTENTIAL CELLS FROM MOUSE EMBRYOS [J].
EVANS, MJ ;
KAUFMAN, MH .
NATURE, 1981, 292 (5819) :154-156
[9]   Histone variant H2A.Z is required for early mammalian development [J].
Faast, R ;
Thonglairoam, V ;
Schulz, TC ;
Beall, J ;
Wells, JRE ;
Taylor, H ;
Matthaei, K ;
Rathjen, PD ;
Tremethick, DJ ;
Lyons, I .
CURRENT BIOLOGY, 2001, 11 (15) :1183-1187
[10]   Requirement for Foxd3 in maintaining pluripotent cells of the early mouse embryo [J].
Hanna, LA ;
Foreman, RK ;
Tarasenko, IA ;
Kessler, DS ;
Labosky, PA .
GENES & DEVELOPMENT, 2002, 16 (20) :2650-2661