正在进行分化的小鼠胚胎干细胞的生长需要6-磷酸果糖-2-激酶/果糖-2,6-二磷酸酶-3的表达增加。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2023-02-01 Epub Date: 2022-11-10 DOI:10.1007/s10616-022-00557-9
Saime Guzel, Yunus Gurpinar, Tugba Hazal Altunok, Abdullah Yalcin
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引用次数: 0

摘要

胚胎干细胞的无限增殖能力及其分化成多种细胞类型的能力,使其成为研究自我更新和多能状态过渡的分子机制的一个有吸引力的候选对象。尽管人们已经研究了6-磷酸果糖-2-激酶/果糖-2,6-二磷酸酶家族(PFKFB1-4)在肿瘤细胞的存活、增殖和分化中的作用,但它们在小鼠ESC(mESC)生物学中的作用目前还不清楚。在本研究中,我们分析了在白血病抑制因子(LIF)存在和不存在的情况下培养的 R1 和 J1 mESC 中 Pfkfb 同工酶的表达。我们报告说,当移除 LIF 后促进 mESCs 分化时,Pfkfb3 同工酶的表达明显增加。我们随后证明,Pfkfb3沉默可诱导分化标志物Brachyury,这表明Pfkfb3可能是调节mESCs中胚层分化所必需的。此外,我们还发现,早期分化的 mESCs 的生长需要 Pfkfb3 表达的增加。尽管这些结果提供了有关Pfkfb表达的mESCs早期分化的重要见解,但要了解通过Pfkfb3调控mESCs增殖和早期分化的途径和机制,还需要进一步的机理研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Increased expression of 6-phosphofructo-2-kinase/fructose 2,6-bisphosphatase-3 is required for growth of mouse embryonic stem cells that are undergoing differentiation.

Increased expression of 6-phosphofructo-2-kinase/fructose 2,6-bisphosphatase-3 is required for growth of mouse embryonic stem cells that are undergoing differentiation.

The unlimited proliferation capacity of embryonic stem cells (ESCs) coupled with their capability to differentiate into several cell types makes them an attractive candidate for studying the molecular mechanisms regulating self-renewal and transition from pluripotent state. Although the roles of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase family (PFKFB1-4) in cell survival, proliferation, and differentiation in tumor cells have been studied, their role in mouse ESC (mESC) biology is currently unkown. In the current study, Pfkfb isoenzyme expressions were analyzed in R1 and J1 mESCs that were cultured in the presence and absence of leukemia inhibitory factor (LIF). We report that expression of the Pfkfb3 isoenzyme was markedly increased when mESCs were promoted to differentiate upon LIF removal. We then demonstrated that Pfkfb3 silencing induced the differentiation marker Brachyury suggesting that Pfkfb3 may be required for the regulation of mesodermal differentiation of mESCs. Furthermore, we show that the increase in Pfkfb3 expression is required for the growth of early differentiated mESCs. Although these results provide important insights into the early differentiation of mESCs with regard to Pfkfb expressions, further mechanistic studies will be needed for understanding the pathways and mechanisms involved in regulation of proliferation and early differentiation of mESCs through Pfkfb3.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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