Institute of Cytology, Russian Academy of Sciences, St-Petersburg, Russian Federation; Saint-Petersburg State University, St-Petersburg, Russian Federation.
Institute of Cytology, Russian Academy of Sciences, St-Petersburg, Russian Federation.
Biochem Biophys Res Commun. 2020 Nov 5;532(2):280-284. doi: 10.1016/j.bbrc.2020.07.133. Epub 2020 Aug 29.
Defective pluripotent cells are removed from embryos prior to differentiation, presumably due to upregulation of the p53 pathway. However, the mechanism underlying p53 protein activation is still unknown. Embryonic stem cells (ESCs), corresponding to cells of the preimplantation blastocyst, likely have similar mechanisms for abnormal cell elimination. Using a mouse ESC cell line with inducible ulk1 gene expression, we showed that Ulk1 upregulation is accompanied by p53 phosphorylation on Ser15. ESCs tolerated the activated p53 and did not undergo apoptosis or cell cycle blockade upon Ulk1 overexpression. However, massive cell death was observed after retinoic acid treatment, suggesting a role of Ulk1-induced p53 activation in the elimination of defective pluripotent cells prior to differentiation.
有缺陷的多能细胞在分化前从胚胎中被清除,这可能是由于 p53 途径的上调。然而,p53 蛋白激活的机制尚不清楚。胚胎干细胞(ESCs)对应于着床前囊胚的细胞,可能具有类似的异常细胞清除机制。我们使用带有诱导性 ulk1 基因表达的小鼠 ESC 细胞系表明,Ulk1 的上调伴随着 p53 在丝氨酸 15 上的磷酸化。ESCs 耐受激活的 p53,并且在 Ulk1 过表达时不会经历细胞凋亡或细胞周期阻滞。然而,在用维甲酸处理后观察到大量细胞死亡,这表明 Ulk1 诱导的 p53 激活在分化前有缺陷的多能细胞的清除中起作用。