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本文引用的文献

1
Chronic endometritis modifies decidualization in human endometrial stromal cells.慢性子宫内膜炎会改变人子宫内膜基质细胞的蜕膜化过程。
Reprod Biol Endocrinol. 2017 Mar 4;15(1):16. doi: 10.1186/s12958-017-0233-x.
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Epigenetic mechanisms in endometrial cancer.子宫内膜癌中的表观遗传机制。
J BUON. 2016 Mar-Apr;21(2):301-6.
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The Multifaceted Actions of Leukaemia Inhibitory Factor in Mediating Uterine Receptivity and Embryo Implantation.白血病抑制因子在介导子宫容受性和胚胎着床中的多方面作用
Am J Reprod Immunol. 2016 Mar;75(3):246-55. doi: 10.1111/aji.12474. Epub 2016 Jan 28.
4
The Histone Methyltransferase Inhibitor BIX01294 Inhibits HIF-1α Stability and Angiogenesis.组蛋白甲基转移酶抑制剂BIX01294抑制缺氧诱导因子-1α稳定性及血管生成。
Mol Cells. 2015 Jun;38(6):528-34. doi: 10.14348/molcells.2015.0026. Epub 2015 May 27.
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Endometrial stromal cells and decidualized stromal cells: origins, transformation and functions.子宫内膜基质细胞与蜕膜化基质细胞:起源、转化及功能
Gene. 2014 Nov 1;551(1):1-14. doi: 10.1016/j.gene.2014.08.047. Epub 2014 Aug 26.
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BIX-01294 induces autophagy-associated cell death via EHMT2/G9a dysfunction and intracellular reactive oxygen species production.BIX-01294 通过 EHMT2/G9a 功能障碍和细胞内活性氧产生诱导自噬相关细胞死亡。
Autophagy. 2013 Dec;9(12):2126-39. doi: 10.4161/auto.26308.
7
Histone-lysine methyltransferase EHMT2 is involved in proliferation, apoptosis, cell invasion, and DNA methylation of human neuroblastoma cells.组蛋白赖氨酸甲基转移酶 EHMT2 参与人神经母细胞瘤细胞的增殖、凋亡、细胞侵袭和 DNA 甲基化。
Anticancer Drugs. 2013 Jun;24(5):484-93. doi: 10.1097/CAD.0b013e32835ffdbb.
8
Distinct spatiotemporal expression of serine proteases Prss23 and Prss35 in periimplantation mouse uterus and dispensable function of Prss35 in fertility.丝氨酸蛋白酶 Prss23 和 Prss35 在着床期小鼠子宫中的时空特异性表达及 Prss35 在生育中的非必需功能。
PLoS One. 2013;8(2):e56757. doi: 10.1371/journal.pone.0056757. Epub 2013 Feb 22.
9
Decidual-secreted factors alter invasive trophoblast membrane and secreted proteins implying a role for decidual cell regulation of placentation.蜕膜分泌因子改变侵袭性滋养层细胞膜和分泌蛋白,提示蜕膜细胞在胎盘形成中的调节作用。
PLoS One. 2012;7(2):e31418. doi: 10.1371/journal.pone.0031418. Epub 2012 Feb 16.
10
Successful preimplantation genetic aneuploidy screening in Turkish patients.土耳其患者成功进行植入前基因非整倍体筛查
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[甲基转移酶抑制剂BIX01294促进小鼠子宫基质细胞体外迁移并抑制其蜕膜化]

[Methyltransferase inhibitor BIX01294 promotes the migration and inhibits decidualization of mouse uterine stromal cells in vitro].

作者信息

Liao Hui-Qi, Tian Liu, Yang Hui, Ma Ni, Zhang Chang-Jun, Diao Hong-Lu

机构信息

1Reproductive Medicine Center, People's Hospital Affiliated to Hubei University of Medicine, 2School of Biomedical Engineering, Hubei University of Medicine, Shiyan 442000, China. E-mail:

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2017 Jun 20;37(6):730-736. doi: 10.3969/j.issn.1673-4254.2017.06.03.

DOI:10.3969/j.issn.1673-4254.2017.06.03
PMID:28669944
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6744149/
Abstract

OBJECTIVE

To investigate the effect of BIX01294 (BIX), a methyltransferase inhibitor, on the migration and decidualization of the stromal cells in mouse uterus.

METHODS

Mouse endometrial stromal cells were isolated and cultured from the uterus of pregnant mice on day 3.5 of gestation. The migration and decidualization of mouse endometrial stromal cells treated with BIX at different concentrations were observed with wound healing assay and real-time PCR.

RESULTS

The migration distance of mouse endometrial stromal cells increased as the BIX concentration increased within the range below 15 µmol/L. Compared with the control cells, the cells treated with BIX (15 µmol/L) showed significantly increased migration distances, but increasing BIX concentration to 20 µmol/L did not further increase the cell migration distance and began to cause cell death. Compared with the control cells, the BIX-treated stromal cells exhibited significantly down-regulated expression of Ehmt2 mRNA, and 15 µmol/L BIX caused inhibition of decidualization in the stromal cells.

CONCLUSION

Within a defined concentration range, BIX promotes the migration and inhibits decidualization of mouse uterine stromal cells by inhibiting the expression of Ehmt2 mRNA.

摘要

目的

研究甲基转移酶抑制剂BIX01294(BIX)对小鼠子宫基质细胞迁移和蜕膜化的影响。

方法

从妊娠第3.5天的孕鼠子宫中分离并培养小鼠子宫内膜基质细胞。采用划痕愈合试验和实时定量PCR观察不同浓度BIX处理的小鼠子宫内膜基质细胞的迁移和蜕膜化情况。

结果

在低于15 μmol/L的范围内,小鼠子宫内膜基质细胞的迁移距离随BIX浓度的增加而增加。与对照细胞相比,用BIX(15 μmol/L)处理的细胞迁移距离显著增加,但将BIX浓度提高到20 μmol/L并未进一步增加细胞迁移距离,且开始导致细胞死亡。与对照细胞相比,BIX处理的基质细胞中Ehmt2 mRNA表达显著下调,15 μmol/L BIX可抑制基质细胞的蜕膜化。

结论

在一定浓度范围内,BIX通过抑制Ehmt2 mRNA的表达促进小鼠子宫基质细胞的迁移并抑制其蜕膜化。