Zap70 Functions to Maintain Stemness of Mouse Embryonic Stem Cells by Negatively Regulating Jak1/Stat3/c-Myc Signaling

被引:26
作者
Cha, Young [2 ]
Moon, Bo-hyun
Lee, Mi-ok [2 ]
Ahn, Hee-jin [2 ]
Lee, Hye-jin
Lee, Kyung-ah [2 ]
Fornace, Albert J., Jr. [3 ]
Kim, Kwang-soo [4 ]
Cha, Hyuk-jin [2 ]
Park, Kyung-soon [1 ,2 ]
机构
[1] CHA Univ, Coll Life Sci, Dept Biomed Sci, CHA Stem Cell Inst, Seoul 135081, South Korea
[2] CHA Univ, Coll Life Sci, Dept Biomed Sci, Pochon Si, Gyeonggi Do, South Korea
[3] Georgetown Univ, Dept Biochem & Mol & Cellular Biol, Washington, DC USA
[4] Harvard Univ, McLean Hosp, Sch Med, Mol Neurobiol Lab, Belmont, MA 02178 USA
关键词
Zap70; Mouse embryonic stem cells; Jak/; Stat3; c-Myc; SHP-1; LIFR; Self-renewal; Pluripotency; Stemness; CHRONIC LYMPHOCYTIC-LEUKEMIA; TYROSINE PHOSPHATASE; SELF-RENEWAL; INHIBITORY FACTOR; STAT3; ACTIVATION; EXPRESSION; ZAP-70; GENE; DIFFERENTIATION; KINASE;
D O I
10.1002/stem.470
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Zeta-chain-associated protein kinase-70 (Zap70), a Syk family tyrosine kinase, has been reported to be present exclusively in normal T-cells, natural killer cells, and B cells, serving as a pivotal regulator of antigen-mediated receptor signaling and development. In this study, we report that Zap70 is expressed in undifferentiated mouse embryonic stem cells (mESCs) and may critically regulate selfrenewal and pluripotency in mESCs. We found that Zap70 knocked-down mESCs (Zap70KD) show sustained self-renewal and defective differentiation. In addition, we present evidence that the sustained self-renewal in Zap70KD is associated with enhanced Jak/Stat3 signaling and c-Myc induction. These altered signaling appears to result from upregulated leukemia inhibitory factor receptor and downregulated src homology region 2 domain containing phosphatase 1 (SHP-1) phosphatase activity. On the basis of these results, we propose that in undifferentiated mESCs, Zap70 plays important roles in modulating the balance between self-renewal capacity and pluripotent differentiation ability as a key regulator of the Jak/Stat3/ c-Myc signaling pathway. STEM CELLS 2010; 127: 1476-1486
引用
收藏
页码:1476 / 1486
页数:11
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