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抑制二甲基亚砜诱导培养的小鼠红白血病细胞的红细胞生成分化。

Inhibition of dimethyl sulfoxide induced erythropoietic differentiation of murine erythroleukemia cells in culture.

作者信息

Foresti M, Gaudio L, Geraci G, Manduca P

出版信息

Cancer Res. 1986 Dec;46(12 Pt 1):6260-3.

PMID:3096558
Abstract

The dimethyl sulfoxide induced erythropoietic differentiation of murine erythroleukemia cells, as determined by scoring benzidine positive cells, is inhibited by mitomycin C at concentrations that have no effect on cell proliferation. The inhibition occurs only when cells are treated with mitomycin C during induction and has a limit value of about 50%, independent of mitomycin C concentration. This limit value does not depend on cell heterogeneity since genetically homogeneous subclones, derived from DS19 clone, show levels of mitomycin C inhibition between 16 and 50%. Treatment with mitomycin C at different times after dimethyl sulfoxide addition shows that cell sensitivity to inhibition is not homogeneous during the induction period; it is maximal between 18 and 24 h from the start of induction and is observed with a concentration of mitomycin C as low as 25 fM. The inhibition of the benzidine positive phenotypic expression appears irreversible since this effect is observed on cells even several generations after those which were actually treated.

摘要

通过对联苯胺阳性细胞进行计数来确定,二甲基亚砜诱导的小鼠红白血病细胞的红细胞生成分化受到丝裂霉素C的抑制,而丝裂霉素C的浓度对细胞增殖没有影响。这种抑制仅在诱导过程中用丝裂霉素C处理细胞时才会发生,并且具有约50%的极限值,与丝裂霉素C的浓度无关。该极限值不依赖于细胞异质性,因为源自DS19克隆的基因同质亚克隆显示丝裂霉素C的抑制水平在16%至50%之间。在添加二甲基亚砜后的不同时间用丝裂霉素C处理表明,在诱导期细胞对抑制的敏感性是不均匀的;在诱导开始后的18至24小时之间敏感性最高,并且在低至25 fM的丝裂霉素C浓度下也可观察到。联苯胺阳性表型表达的抑制似乎是不可逆的,因为即使在实际处理后的几代细胞中也能观察到这种效应。

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