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引用本文的文献

1
Expression of Pfkfb isoenzymes during in vitro differentiation of mouse embryonic stem cells into insulin-producing cells.在体外将小鼠胚胎干细胞分化为胰岛素生成细胞过程中 Pfkfb 同工酶的表达。
Turk J Med Sci. 2023 Aug 11;53(6):1565-1573. doi: 10.55730/1300-0144.5725. eCollection 2023.

本文引用的文献

1
PFKFB3-dependent glucose metabolism regulates 3T3-L1 adipocyte development.PFKFB3 依赖性糖代谢调节 3T3-L1 脂肪细胞发育。
FASEB J. 2021 Jul;35(7):e21728. doi: 10.1096/fj.202100381RR.
2
Energy Metabolism Regulates Stem Cell Pluripotency.能量代谢调节干细胞多能性。
Front Cell Dev Biol. 2020 Feb 28;8:87. doi: 10.3389/fcell.2020.00087. eCollection 2020.
3
Stem cells: past, present, and future.干细胞:过去、现在和未来。
Stem Cell Res Ther. 2019 Feb 26;10(1):68. doi: 10.1186/s13287-019-1165-5.
4
PFKFB3 is involved in breast cancer proliferation, migration, invasion and angiogenesis.PFKFB3 参与乳腺癌的增殖、迁移、浸润和血管生成。
Int J Oncol. 2018 Mar;52(3):945-954. doi: 10.3892/ijo.2018.4257. Epub 2018 Jan 30.
5
Metabolic control of primed human pluripotent stem cell fate and function by the miR-200c-SIRT2 axis.通过miR-200c-SIRT2轴对预激活的人类多能干细胞命运和功能的代谢控制
Nat Cell Biol. 2017 May;19(5):445-456. doi: 10.1038/ncb3517. Epub 2017 Apr 24.
6
The metabolic programming of stem cells.干细胞的代谢编程
Genes Dev. 2017 Feb 15;31(4):336-346. doi: 10.1101/gad.293167.116. Epub 2017 Mar 17.
7
Metabolic remodeling during the loss and acquisition of pluripotency.多能性丧失与获得过程中的代谢重塑。
Development. 2017 Feb 15;144(4):541-551. doi: 10.1242/dev.128389.
8
PFKFB3, a Direct Target of p63, Is Required for Proliferation and Inhibits Differentiation in Epidermal Keratinocytes.PFKFB3是p63的直接靶点,对表皮角质形成细胞的增殖是必需的,并抑制其分化。
J Invest Dermatol. 2017 Jun;137(6):1267-1276. doi: 10.1016/j.jid.2016.12.020. Epub 2017 Jan 17.
9
Dynamic Heterogeneity of Brachyury in Mouse Epiblast Stem Cells Mediates Distinct Response to Extrinsic Bone Morphogenetic Protein (BMP) Signaling.小鼠上胚层干细胞中 Brachyury 的动态异质性介导了对外源性骨形态发生蛋白(BMP)信号的不同反应。
J Biol Chem. 2016 Jul 15;291(29):15212-25. doi: 10.1074/jbc.M115.705418. Epub 2016 May 16.
10
Putative oncogene Brachyury (T) is essential to specify cell fate but dispensable for notochord progenitor proliferation and EMT.推定癌基因短尾(T)对于确定细胞命运至关重要,但对于脊索祖细胞增殖和上皮-间质转化并非必需。
Proc Natl Acad Sci U S A. 2016 Apr 5;113(14):3820-5. doi: 10.1073/pnas.1601252113. Epub 2016 Mar 22.

正在经历分化的小鼠胚胎干细胞生长需要6-磷酸果糖-2-激酶/果糖-2,6-二磷酸酶-3的表达增加。

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.

作者信息

Guzel Saime, Gurpinar Yunus, Altunok Tugba Hazal, Yalcin Abdullah

机构信息

Department of Biochemistry, School of Veterinary Medicine, Bursa Uludag University, Bursa, Turkey.

Research Center for Translational Medicine, Koc University, 34010 Istanbul, Turkey.

出版信息

Cytotechnology. 2023 Feb;75(1):27-38. doi: 10.1007/s10616-022-00557-9. Epub 2022 Nov 10.

DOI:10.1007/s10616-022-00557-9
PMID:36713065
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9880118/
Abstract

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.

摘要

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。