PAX7 Balances the Cell Cycle Progression via Regulating Expression of Dnmt3b and Apobec2 in Differentiating PSCs

被引:3
作者
Florkowska, Anita [1 ]
Meszka, Igor [1 ]
Nowacka, Joanna [1 ]
Granica, Monika [1 ]
Jablonska, Zuzanna [1 ]
Zawada, Magdalena [1 ]
Truszkowski, Lukasz [1 ]
Ciemerych, Maria A. [1 ]
Grabowska, Iwona [1 ]
机构
[1] Univ Warsaw, Fac Biol, Inst Dev Biol & Biomed Sci, Dept Cytol, Miecznikowa 1, PL-02096 Warsaw, Poland
关键词
mouse; ESCs; iPSCs; stem cells; differentiation; myogenesis; cell cycle; skeletal muscle; teratoma; Pax7; 5azaC; EMBRYONIC STEM-CELLS; SKELETAL-MUSCLE; IN-VITRO; MYOGENIC DIFFERENTIATION; GENE-EXPRESSION; SATELLITE CELLS; HUMAN ES; DISTINCT; BODIES; D3;
D O I
10.3390/cells10092205
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
PAX7 transcription factor plays a crucial role in embryonic myogenesis and in adult muscles in which it secures proper function of satellite cells, including regulation of their self renewal. PAX7 downregulation is necessary for the myogenic differentiation of satellite cells induced after muscle damage, what is prerequisite step for regeneration. Using differentiating pluripotent stem cells we documented that the absence of functional PAX7 facilitates proliferation. Such action is executed by the modulation of the expression of two proteins involved in the DNA methylation, i.e., Dnmt3b and Apobec2. Increase in Dnmt3b expression led to the downregulation of the CDK inhibitors and facilitated cell cycle progression. Changes in Apobec2 expression, on the other hand, differently impacted proliferation/differentiation balance, depending on the experimental model used.
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页数:19
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