Guzel Saime, Gurpinar Yunus, Altunok Tugba Hazal, Yalcin Abdullah
Department of Biochemistry, School of Veterinary Medicine, Bursa Uludag University, Bursa, Turkey.
Research Center for Translational Medicine, Koc University, 34010 Istanbul, Turkey.
Cytotechnology. 2023 Feb;75(1):27-38. doi: 10.1007/s10616-022-00557-9. Epub 2022 Nov 10.
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.
胚胎干细胞(ESCs)具有无限增殖能力,且能够分化为多种细胞类型,这使其成为研究调控自我更新及从多能状态转变的分子机制的极具吸引力的候选对象。尽管已对6-磷酸果糖-2-激酶/果糖-2,6-二磷酸酶家族(PFKFB1-4)在肿瘤细胞的细胞存活、增殖和分化中的作用进行了研究,但其在小鼠胚胎干细胞(mESC)生物学中的作用目前尚不清楚。在本研究中,分析了在有和没有白血病抑制因子(LIF)存在的情况下培养的R1和J1 mESC中Pfkfb同工酶的表达。我们报告称,当去除LIF促使mESC分化时,Pfkfb3同工酶的表达显著增加。然后我们证明,Pfkfb3沉默诱导了分化标志物Brachyury,这表明Pfkfb3可能是调控mESC中胚层分化所必需的。此外,我们表明,Pfkfb3表达的增加是早期分化的mESC生长所必需的。尽管这些结果为mESC早期分化过程中Pfkfb表达提供了重要见解,但仍需要进一步的机制研究来了解通过Pfkfb3调控mESC增殖和早期分化所涉及的途径和机制。