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TPA或二甲基亚砜诱导HL60细胞分化过程中G2相关基因的不同反应。

Differing responses of G2-related genes during differentiation of HL60 cells induced by TPA or DMSO.

作者信息

Horiguchi-Yamada J, Yamada H

机构信息

Department of Internal Medicine, Aoto Hospital, Jikei University School of Medicine, Tokyo, Japan.

出版信息

Mol Cell Biochem. 1993 Feb 17;119(1-2):29-34. doi: 10.1007/BF00926850.

DOI:10.1007/BF00926850
PMID:8455582
Abstract

Differentiation leads to the cessation of cellular proliferation, but little is known about the molecular mechanisms of growth arrest. We compared the effect of two differentiation inducers, 12-o-tetradecanoyl 13-acetate (TPA) and dimethyl sulfoxide (DMSO) on both the cell-cycle and the modulation of G2-related genes in synchronized HL60 cells. TPA treatment of HL60 cells resulted in G1 arrest within 24 h. In contrast, the cell cycling of DMSO-treated cells was initially accelerated and they progressed to the second cycle before accumulating in the G1 phase. Expression of cyclin B, cdc25, wee1 and cdc2 was studied during cell cycle arrest by Northern blot hybridization. Expression of cyclin B, cdc25 and cdc2 fluctuated in association with cell cycle progression towards the G2/M phase, while wee1 expression remained constant in untreated cells. These four genes were highly expressed in TPA-treated cells for the first 12 h, but drastic down-regulation was seen at 18 h and expression became undetectable after 24 h. In contrast, no remarked changes of gene expression were seen in DMSO-treated cells. These findings suggest that cell cycle progression along with the initial process of differentiation in response to TPA differs from the response to DMSO and that the down-regulation of cdc2 expression by TPA-treated HL60 cells contributes to endorsement of G1 arrest.

摘要

分化导致细胞增殖停止,但对于生长停滞的分子机制却知之甚少。我们比较了两种分化诱导剂,即12-O-十四烷酰佛波醇-13-乙酸酯(TPA)和二甲基亚砜(DMSO)对同步化的HL60细胞的细胞周期以及G2相关基因调控的影响。用TPA处理HL60细胞会在24小时内导致G1期停滞。相反,用DMSO处理的细胞的细胞周期最初会加速,并且它们在进入G1期积累之前会进入第二个周期。通过Northern印迹杂交研究了细胞周期停滞期间细胞周期蛋白B、细胞分裂周期蛋白25(cdc25)、wee1和细胞周期蛋白依赖性激酶2(cdc2)的表达。细胞周期蛋白B、cdc25和cdc2的表达随着细胞周期向G2/M期的进展而波动,而wee1的表达在未处理的细胞中保持恒定。这四个基因在TPA处理的细胞中最初12小时高表达,但在18小时时出现急剧下调,24小时后表达变得不可检测。相反,在DMSO处理的细胞中未观察到基因表达的明显变化。这些发现表明,响应TPA的细胞周期进展以及分化的初始过程与对DMSO的反应不同,并且TPA处理的HL60细胞中cdc2表达的下调有助于维持G1期停滞。

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