• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

一氯胺诱导 K562 红白血病细胞向红系和巨核系分化。

Erythroid and megakaryocytic differentiation of K562 erythroleukemic cells by monochloramine.

机构信息

Department of Nursing Science, Faculty of Health and Welfare, Okayama Prefectural University , Soja , Japan.

出版信息

Free Radic Res. 2014 Mar;48(3):292-302. doi: 10.3109/10715762.2013.865840. Epub 2014 Jan 7.

DOI:10.3109/10715762.2013.865840
PMID:24237253
Abstract

The induction of leukemic cell differentiation is a hopeful therapeutic modality. We studied the effects of monochloramine (NH2Cl) on erythroleukemic K562 cell differentiation, and compared the effects observed with those of U0126 and staurosporine, which are known inducers of erythroid and megakaryocytic differentiation, respectively. CD235 (glycophorin) expression, a marker of erythroid differentiation, was significantly increased by NH2Cl and U0126, along with an increase in cd235 mRNA levels. Other erythroid markers such as γ-globin and CD71 (transferrin receptor) were also increased by NH2Cl and U0126. In contrast, CD61 (integrin β3) and CD42b (GP1bα) expression, markers of megakaryocytic differentiation, was increased by staurosporine, but did not change significantly by NH2Cl and U0126. NH2Cl retarded cell proliferation without a marked loss of viability. When ERK phosphorylation (T202/Y204) and CD235 expression were compared using various chemicals, a strong negative correlation was observed (r = -0.76). Paradoxically, NH2Cl and staurosporine, but not U0126, induced large cells with multiple or lobulated nuclei, which was characteristic to megakaryocytes. NH2Cl increased the mRNA levels of gata1 and scl, decreased that of gata2, and did not change those of pu.1 and klf1. The changes observed in mRNA expression were different from those of U0126 or staurosporine. These results suggest that NH2Cl induces the bidirectional differentiation of K562. Oxidative stress may be effective in inducing leukemic cell differentiation.

摘要

诱导白血病细胞分化是一种有前途的治疗方法。我们研究了单氯胺(NH2Cl)对红白血病 K562 细胞分化的影响,并将观察到的效果与 U0126 和 staurosporine 的效果进行了比较,这两种药物分别是红细胞生成和巨核细胞分化的已知诱导剂。CD235(糖蛋白)表达,红细胞分化的标志物,明显增加了 NH2Cl 和 U0126,同时 CD235mRNA 水平也增加了。其他红细胞标志物,如γ-球蛋白和 CD71(转铁蛋白受体),也被 NH2Cl 和 U0126 增加。相比之下,CD61(整合素β3)和 CD42b(GP1bα)的表达,巨核细胞分化的标志物,是由 staurosporine 增加,但没有明显变化由 NH2Cl 和 U0126。NH2Cl 延缓细胞增殖,而不会显著降低细胞活力。当使用各种化学物质比较 ERK 磷酸化(T202/Y204)和 CD235 表达时,观察到强烈的负相关(r = -0.76)。矛盾的是,NH2Cl 和 staurosporine,但不是 U0126,诱导具有多个或叶状核的大细胞,这是巨核细胞的特征。NH2Cl 增加了 gata1 和 scl 的 mRNA 水平,降低了 gata2 的水平,而 pu.1 和 klf1 的水平没有变化。mRNA 表达的变化与 U0126 或 staurosporine 的变化不同。这些结果表明 NH2Cl 诱导 K562 的双向分化。氧化应激可能有效诱导白血病细胞分化。

相似文献

1
Erythroid and megakaryocytic differentiation of K562 erythroleukemic cells by monochloramine.一氯胺诱导 K562 红白血病细胞向红系和巨核系分化。
Free Radic Res. 2014 Mar;48(3):292-302. doi: 10.3109/10715762.2013.865840. Epub 2014 Jan 7.
2
Effects of chebulinic acid on differentiation of human leukemia K562 cells.诃子林檎酸对人白血病K562细胞分化的影响。
Acta Pharmacol Sin. 2004 Feb;25(2):231-8.
3
CDDO-Im is a stimulator of megakaryocytic differentiation.CDDO-Im 是巨核细胞分化的刺激剂。
Leuk Res. 2011 Apr;35(4):534-44. doi: 10.1016/j.leukres.2010.09.013. Epub 2010 Oct 29.
4
The alpha1-adrenergic receptor antagonists, benoxathian and prazosin, induce apoptosis and a switch towards megakaryocytic differentiation in human erythroleukemia cells.α1-肾上腺素能受体拮抗剂贝诺沙硫和哌唑嗪可诱导人红白血病细胞凋亡并向巨核细胞分化转变。
Ann Hematol. 2009 Oct;88(10):989-97. doi: 10.1007/s00277-009-0704-z. Epub 2009 Feb 25.
5
Levels of Smad7 regulate Smad and mitogen activated kinases (MAPKs) signaling and controls erythroid and megakaryocytic differentiation of erythroleukemia cells.Smad7的水平调节Smad和丝裂原活化蛋白激酶(MAPK)信号传导,并控制红白血病细胞的红系和巨核系分化。
Platelets. 2007 Dec;18(8):566-78. doi: 10.1080/09537100701549546.
6
A screen for Fli-1 transcriptional modulators identifies PKC agonists that induce erythroid to megakaryocytic differentiation and suppress leukemogenesis.一项针对Fli-1转录调节因子的筛选鉴定出了能诱导红系向巨核系分化并抑制白血病发生的蛋白激酶C激动剂。
Oncotarget. 2017 Mar 7;8(10):16728-16743. doi: 10.18632/oncotarget.14377.
7
A multifunctional 5-aminolevulinic acid derivative induces erythroid differentiation of K562 human erythroleukemic cells.一种多功能 5-氨基酮戊酸衍生物可诱导 K562 人红白血病细胞向红系分化。
Eur J Pharm Sci. 2012 Aug 30;47(1):206-14. doi: 10.1016/j.ejps.2012.05.017. Epub 2012 Jun 13.
8
Induced myeloid differentiation of K562 cells with downregulation of erythroid and megakaryocytic transcription factors: a novel experimental model for hemopoietic lineage restriction.
Exp Hematol. 1993 Apr;21(4):525-31.
9
Expression of megakaryocytic and erythroid properties in human leukemic cells.人类白血病细胞中巨核细胞和红细胞特性的表达。
Exp Hematol. 1996 Feb;24(2):158-68.
10
Erk pathway inhibitor U0126 induces gamma-globin expression in erythroid cells.细胞外信号调节激酶(Erk)通路抑制剂U0126可诱导红系细胞中γ-珠蛋白的表达。
Cell Mol Biol (Noisy-le-grand). 2005 Sep 5;51(2):215-27.

引用本文的文献

1
Utilization of Dairy By-Products as a Source of Functional and Health Compounds-The Role of Ovine Colostrum and Milk Whey on Chronic Myeloid Leukemia Cells.利用乳制品副产品作为功能性和健康化合物的来源——绵羊初乳和乳清对慢性粒细胞白血病细胞的作用
Foods. 2023 Apr 23;12(9):1752. doi: 10.3390/foods12091752.
2
Polycomb Factor PHF19 Controls Cell Growth and Differentiation Toward Erythroid Pathway in Chronic Myeloid Leukemia Cells.多梳因子PHF19调控慢性粒细胞白血病细胞向红系途径的细胞生长和分化。
Front Cell Dev Biol. 2021 Apr 29;9:655201. doi: 10.3389/fcell.2021.655201. eCollection 2021.
3
H3K27me3-rich genomic regions can function as silencers to repress gene expression via chromatin interactions.
富含 H3K27me3 的基因组区域可以通过染色质相互作用作为抑制子发挥作用,从而抑制基因表达。
Nat Commun. 2021 Jan 29;12(1):719. doi: 10.1038/s41467-021-20940-y.
4
Cancer Stem Cells: Emergent Nature of Tumor Emergency.癌症干细胞:肿瘤急症的新特性
Front Genet. 2018 Nov 16;9:544. doi: 10.3389/fgene.2018.00544. eCollection 2018.