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本文引用的文献

1
Small molecule antagonists of cell-surface heparan sulfate and heparin-protein interactions.细胞表面硫酸乙酰肝素及肝素-蛋白质相互作用的小分子拮抗剂
Chem Sci. 2015 Oct 1;6(10):5984-5993. doi: 10.1039/c5sc01208b. Epub 2015 Jul 29.
2
Genomic Instability of iPSCs: Challenges Towards Their Clinical Applications.iPS 细胞的基因组不稳定性:其临床应用面临的挑战。
Stem Cell Rev Rep. 2017 Feb;13(1):7-16. doi: 10.1007/s12015-016-9680-6.
3
Glycosyltransferase ST6GAL1 contributes to the regulation of pluripotency in human pluripotent stem cells.糖基转移酶ST6GAL1有助于调控人类多能干细胞的多能性。
Sci Rep. 2015 Aug 25;5:13317. doi: 10.1038/srep13317.
4
Leukemia inhibitory factor (LIF).白血病抑制因子(LIF)。
Cytokine Growth Factor Rev. 2015 Oct;26(5):533-44. doi: 10.1016/j.cytogfr.2015.07.001. Epub 2015 Jul 4.
5
A common sugar-nucleotide-mediated mechanism of inhibition of (glycosamino)glycan biosynthesis, as evidenced by 6F-GalNAc (Ac3).一种常见的糖核苷酸介导的(糖胺)聚糖生物合成抑制机制,如6F-GalNAc(Ac3)所示。
FASEB J. 2015 Jul;29(7):2993-3002. doi: 10.1096/fj.14-264226. Epub 2015 Apr 13.
6
Chondroitin sulfate is indispensable for pluripotency and differentiation of mouse embryonic stem cells.硫酸软骨素对于小鼠胚胎干细胞的多能性和分化是不可或缺的。
Sci Rep. 2014 Jan 15;4:3701. doi: 10.1038/srep03701.
7
Murine T cell activation is regulated by surfen (bis-2-methyl-4-amino-quinolyl-6-carbamide).鼠 T 细胞的激活受 surfen(双-2-甲基-4-氨基喹啉-6-甲酰胺)调节。
Biochem Biophys Res Commun. 2014 Jan 10;443(2):524-30. doi: 10.1016/j.bbrc.2013.11.119. Epub 2013 Dec 6.
8
Chemical approaches to stem cell biology and therapeutics.化学方法在干细胞生物学和治疗学中的应用。
Cell Stem Cell. 2013 Sep 5;13(3):270-83. doi: 10.1016/j.stem.2013.08.002.
9
Quantitative phosphoproteomics analysis reveals broad regulatory role of heparan sulfate on endothelial signaling.定量磷酸化蛋白质组学分析揭示了硫酸乙酰肝素对血管内皮信号的广泛调节作用。
Mol Cell Proteomics. 2013 Aug;12(8):2160-73. doi: 10.1074/mcp.M112.026609. Epub 2013 May 6.
10
Small molecules, big roles -- the chemical manipulation of stem cell fate and somatic cell reprogramming.小分子,大作用——化学操纵干细胞命运和体细胞重编程。
J Cell Sci. 2012 Dec 1;125(Pt 23):5609-20. doi: 10.1242/jcs.096032.

小分子细胞表面糖胺聚糖拮抗剂限制小鼠胚胎干细胞的多能状态。

Small Molecule Antagonist of Cell Surface Glycosaminoglycans Restricts Mouse Embryonic Stem Cells in a Pluripotent State.

机构信息

Department of Chemistry and Biochemistry, University of California San Diego, La Jolla, California, USA.

出版信息

Stem Cells. 2018 Jan;36(1):45-54. doi: 10.1002/stem.2714. Epub 2017 Oct 27.

DOI:10.1002/stem.2714
PMID:28984039
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6237099/
Abstract

Recently, the field of stem cell-based regeneration has turned its attention toward chemical approaches for controlling the pluripotency and differentiation of embryonic stem cells (ESCs) using drug-like small molecule modulators. Growth factor receptors or their associated downstream kinases that regulate intracellular signaling pathways during differentiation are typically the targets for these molecules. The glycocalyx, which plays an essential role in actuating responses to growth factors at the cellular boundary, offers an underexplored opportunity for intervention using small molecules to influence differentiation. Here, we show that surfen, an antagonist of cell-surface glycosaminoglycans required for growth factor association with cognate receptors, acts as a potent and general inhibitor of differentiation and promoter of pluripotency in mouse ESCs. This finding shows that drugging the stem cell Glycome with small molecules to silence differentiation cues can provide a powerful new alternative to existing techniques for controlling stem cell fate. Stem Cells 2018;36:45-54.

摘要

最近,基于干细胞的再生领域将注意力转向了化学方法,使用类似药物的小分子调节剂来控制胚胎干细胞(ESCs)的多能性和分化。在分化过程中调节细胞内信号通路的生长因子受体或其相关下游激酶通常是这些分子的靶标。糖萼在触发细胞边界处对生长因子的反应中起着至关重要的作用,为使用小分子进行干预以影响分化提供了一个未被充分探索的机会。在这里,我们表明,surfen 是一种细胞表面糖胺聚糖的拮抗剂,这种糖胺聚糖对于生长因子与同源受体的结合是必需的,它在小鼠 ESCs 中作为一种有效的、普遍的分化抑制剂和多能性促进剂发挥作用。这一发现表明,用小分子对干细胞糖萼进行药物处理以沉默分化信号可以为控制干细胞命运提供一种强大的新选择,这种方法与现有的技术不同。Stem Cells 2018;36:45-54.