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一种对佛波酯耐药的单核细胞白血病细胞系缺乏蛋白激酶C。

A phorbol diester resistant monocytic leukemia cell line is PKC deficient.

作者信息

Ansari N A, Wu M C

机构信息

Division of Biochemistry, University of North Texas/Texas College of Osteopathic Medicine, Denton 76203.

出版信息

Int J Cell Cloning. 1992 Jan;10(1):47-53. doi: 10.1002/stem.5530100108.

Abstract

MIA C51 is a rat monocytic leukemia cell line which exhibits undifferentiated monocytic phenotype in culture. The proliferation of MIA C51 cells was not inhibited by the addition of 12-O-tetradecanoyl-phorbol-13-acetate (TPA, 1 microgram/ml) or phorbol 12, 13 dibutyrate (PDBu, 10 micrograms/ml). Comparison of MIA C51 cells to a phorbol diester-sensitive human monoblastoid U-937 cell line demonstrated that MIA C51 cells contained significantly lower number of PDBu receptors, protein kinase C (PKC) activity, and PKC protein level. Further experiments demonstrated that addition of TPA to MIA C51 cells did not induce the expression of c-fos proto-oncogene; whereas incubation of MIA C51 cells with N6, O2-dibutyryl cyclic adenosine 3',5' monophosphate (Bt2cAMP) resulted in a rapid increase of c-fos mRNA level. Thus, this cell line provides a new system for studying the signal transduction mechanisms in induced monocytic differentiation.

摘要

MIA C51是一种大鼠单核细胞白血病细胞系,在培养中表现出未分化的单核细胞表型。添加12-O-十四酰佛波醇-13-乙酸酯(TPA,1微克/毫升)或佛波醇12,13-二丁酸酯(PDBu,10微克/毫升)不会抑制MIA C51细胞的增殖。将MIA C51细胞与对佛波醇二酯敏感的人单核母细胞样U-937细胞系进行比较,结果表明MIA C51细胞中PDBu受体数量、蛋白激酶C(PKC)活性和PKC蛋白水平显著更低。进一步实验表明,向MIA C51细胞中添加TPA不会诱导原癌基因c-fos的表达;而用N6,O2-二丁酰环腺苷3',5'-单磷酸(Bt2cAMP)孵育MIA C51细胞会导致c-fos mRNA水平迅速升高。因此,该细胞系为研究诱导单核细胞分化中的信号转导机制提供了一个新系统。

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