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Activating transcription factor 3 coordinates differentiation of cardiac and hematopoietic progenitors by regulating glucose metabolism

机译:通过调节葡萄糖代谢,激活转录因子3坐标通过调节葡萄糖代谢的心脏和造血祖细胞分化

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The cardiac and hematopoietic progenitors (CPs and HPs, respectively) in the mesoderm ultimately form a well-organized circulation system, but mechanisms that reconcile their development remain elusive. We found that activating transcription factor 3 ( atf3 ) was highly expressed in the CPs, HPs, and mesoderm, in zebrafish. The atf3 sup?/?/sup mutants exhibited atrial dilated cardiomyopathy and a high ratio of immature myeloid cells. These manifestations were primarily caused by the blockade of differentiation of both CPs and HPs within the anterior lateral plate mesoderm. Mechanistically, Atf3 targets cebpγ to repress slc2a1a -mediated glucose utilization. The high rate of glucose metabolism in atf3 sup?/?/sup mutants inhibited the differentiation of progenitors by changing the redox state. Therefore, atf3 could provide CPs and HPs with metabolic adaptive capacity to changes in glucose levels. Our study provides new insights into the role of atf3 in the coordination of differentiation of CPs and HPs by regulating glucose metabolism.
机译:心脏病和造血祖细胞(分别)中胚层最终形成了一个有组织良好的循环系统,但调和其发展的机制仍然难以捉摸。我们发现激活转录因子3(ATF3)在CPS,HPS和Mesoderm中高度表达斑马鱼。 ATF3 α/α/α/α/α/α/α突变体表现出真菌扩张的心肌病和高比例的未成熟髓样细胞。这些表现的主要是由侧侧板中的CPS和HPS的分化引起的。机械地,ATF3靶向CEBPγ压制SLC2A1A介导的葡萄糖利用。 ATF3 α/α/α/θ/ηs/θ/α/θ/α/α/α/α/α/θs的高速率抑制了通过改变氧化还原状态的祖细胞的分化。因此,ATF3可以提供CPS和HPS,其具有代谢适应性能够改变葡萄糖水平。我们的研究提供了通过调节葡萄糖代谢来协调CPS和HPS的协调的新见解。

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