Suppr超能文献

烟酰胺及相关化合物诱导小鼠红白血病细胞向红系分化

Induction of erythroid differentiation of murine erythroleukemia cells by nicotinamide and related compounds.

作者信息

Terada M, Fujiki H, Marks P A, Sugimura T

出版信息

Proc Natl Acad Sci U S A. 1979 Dec;76(12):6411-4. doi: 10.1073/pnas.76.12.6411.

Abstract

Nicotinamide and its analogues were evaluated for their activity as inducers of differentiation of murine erythroleukemia cells in culture. N'-Methylnicotinamide was the most effective of the compounds tested; at its optimal concentration it was more effective than dimethyl sulfoxide. With 8-10 mM N'-methylnicotinamide, almost all the cells contained hemoglobin (benzidine-reactive) after a 60-hr culture. Commitment to differentiate, assayed by transfer of the cells to semisolid medium without inducers, occurred much earlier and was more extensive with N'-methylnicotinamide than that with dimethyl sulfoxide or nicotinamide. Increase in globin mRNA was greater in the cells cultured with N'-methylnicotinamide than in cells cultured with dimethyl sulfoxide or nicotinamide. The relationship between the inducing activities of nicotinamide analogues and their effect on poly(ADP-ribose) polymerase in vitro was studied. All the compounds studied that had strong inhibitory effects on poly(ADP-ribose) polymerase in vitro induced differentiation of erythroleukemia cells in culture. This property is not a prerequisite of inducers; N'-methylnicotinamide did not inhibit the enzyme in vitro.

摘要

对烟酰胺及其类似物作为培养的小鼠红白血病细胞分化诱导剂的活性进行了评估。N'-甲基烟酰胺是所测试化合物中最有效的;在其最佳浓度下,它比二甲亚砜更有效。用8-10 mM的N'-甲基烟酰胺培养60小时后,几乎所有细胞都含有血红蛋白(联苯胺反应阳性)。通过将细胞转移到无诱导剂的半固体培养基中来检测分化的起始情况,结果显示,与二甲亚砜或烟酰胺相比,N'-甲基烟酰胺诱导分化发生得更早且更广泛。用N'-甲基烟酰胺培养的细胞中珠蛋白mRNA的增加量比用二甲亚砜或烟酰胺培养的细胞更大。研究了烟酰胺类似物的诱导活性与其体外对聚(ADP-核糖)聚合酶的影响之间的关系。所有在体外对聚(ADP-核糖)聚合酶有强烈抑制作用的研究化合物都能在培养中诱导红白血病细胞分化。这种特性不是诱导剂的先决条件;N'-甲基烟酰胺在体外不抑制该酶。

相似文献

2
1-Methylnicotinamide stimulates cell growth and inhibits hemoglobin synthesis in differentiating murine erythroleukemia cells.
Toxicol In Vitro. 2007 Dec;21(8):1656-62. doi: 10.1016/j.tiv.2007.05.017. Epub 2007 Jul 18.

引用本文的文献

4
Poly(ADP-Ribosyl) Code Functions.聚(ADP-核糖基)编码功能
Acta Naturae. 2021 Apr-Jun;13(2):58-69. doi: 10.32607/actanaturae.11089.
5
7
Advances and perspectives of PARP inhibitors.聚(ADP - 核糖)聚合酶抑制剂的进展与前景
Exp Hematol Oncol. 2019 Nov 11;8:29. doi: 10.1186/s40164-019-0154-9. eCollection 2019.
8
Poly-ADP ribosylation in DNA damage response and cancer therapy.聚腺苷二磷酸核糖基化在 DNA 损伤反应和癌症治疗中的作用。
Mutat Res Rev Mutat Res. 2019 Apr-Jun;780:82-91. doi: 10.1016/j.mrrev.2017.09.004. Epub 2017 Sep 20.
10
PARP inhibitors: Synthetic lethality in the clinic.聚(ADP-核糖)聚合酶抑制剂:临床中的合成致死性
Science. 2017 Mar 17;355(6330):1152-1158. doi: 10.1126/science.aam7344. Epub 2017 Mar 16.

本文引用的文献

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