The differential activation of intracellular signaling pathways confers the permissiveness of embryonic stem cell derivation from different mouse strains

被引:19
|
作者
Ohtsuka, Satoshi [1 ]
Niwa, Hitoshi [1 ,2 ,3 ]
机构
[1] RIKEN, CDB, Lab Pluripotent Stem Cell Studies, Chuo Ku, Kobe, Hyogo 6500047, Japan
[2] Japan Sci & Technol Agcy, CREST, Saitama 3320012, Japan
[3] Kobe Univ, Grad Sch Med, Lab Dev & Regenerat Med, Chuo Ku, Kobe, Hyogo 6500017, Japan
来源
DEVELOPMENT | 2015年 / 142卷 / 03期
基金
日本科学技术振兴机构;
关键词
LIF signaling; MAP kinase; Stat3; Embryonic stem cell; Signal responsiveness; SELF-RENEWAL; ES CELLS; RAT BLASTOCYSTS; ESTABLISHMENT; STAT3; LINES; PLURIPOTENCY; FGF; CULTURE; PROTEIN;
D O I
10.1242/dev.112375
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The requirement of leukemia inhibitory factor (LIF) for the establishment and maintenance of mouse embryonic stem cells (ESCs) depends on the genetic background of the ESC origin. To reveal the molecular basis of the strain-dependent function of LIF, we compared the activation of the intracellular signaling pathways downstream of LIF in ESCs with different genetic backgrounds. We found that the JAK-Stat3 pathway was dominantly activated in ESCs derived from 'permissive' mouse strains (129Sv and C57BL6), whereas the MAP kinase pathway was hyperactivated in ESCs from 'non-permissive' strains (NOD, CBA and FVB). Artificial activation of Stat3 supported stable self-renewal of ESCs from non-permissive strains. These data suggest that the difference in the balance between the two intracellular signaling pathways underlies the differential response to LIF.
引用
收藏
页码:431 / 437
页数:7
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