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COUP-TFI 在视黄酸诱导 P19 细胞向内胚层细胞分化中的作用。

Role of COUP-TFI during retinoic acid-induced differentiation of P19 cells to endodermal cells.

机构信息

Departments of Biochemistry, Temple University School of Medicine, Philadelphia, Pennsylvania 19140, USA.

出版信息

J Cell Physiol. 2013 Apr;228(4):791-800. doi: 10.1002/jcp.24228.

Abstract

Retinoic acid (RA) is a positive regulator of P19 cell differentiation. Silencing of pre-B cell leukemia transcription factors (PBXs) expression in P19 cells (AS cells) results in a failure of these cells to differentiate to endodermal cells upon RA treatment. Chicken Ovalbumin Upstream Promoter Transcription Factor I (COUP-TFI) is an orphan member of the steroid-thyroid hormone superfamily. RA treatment of wild type P19 cells results in a dramatic increase in the expression of COUP-TFI; however, COUP-TFI mRNA levels fail to be elevated upon RA treatment of AS cells indicating that PBX expression is required for elevation in COUP-TFI expression. To study the role of COUP-TFI during RA-dependent differentiation of P19 cells, AS cells that inducibly express various levels of COUP-TFI were prepared. Exogenous expression of COUP-TFI in AS cells, in a dose-dependent fashion, leads to growth inhibition, modest cell cycle disruption, and early apoptosis. Furthermore, AS cells can overcome the blockage in RA-dependent differentiation to endodermal cells when either pharmacological levels of COUP-TFI are expressed or a combination of both the expression of physiological levels of COUP-TFI and RA treatment. Additionally, the mRNA level of several pluripotency associated genes including OCT-4, DAX-1, and SF-1 in the COUP-TFI expressing AS cells are reduced. Moreover, analysis of the expression of primary RA response genes indicates that COUP-TFI is involved in the regulatory modulation of the expression of at least two genes, CYP26A1 and HoxA1. These studies demonstrate that COUP-TFI functions as a physiologically relevant regulator during RA-mediated endodermal differentiation of P19 cells.

摘要

视黄酸(RA)是 P19 细胞分化的正调节剂。沉默 P19 细胞(AS 细胞)中的前 B 细胞白血病转录因子(PBXs)表达导致这些细胞在 RA 处理后不能分化为内胚层细胞。鸡卵清蛋白上游启动子转录因子 I(COUP-TFI)是类固醇-甲状腺激素超家族的孤儿成员。RA 处理野生型 P19 细胞导致 COUP-TFI 的表达显著增加;然而,AS 细胞中 RA 处理未能提高 COUP-TFI mRNA 水平,表明 PBX 表达是 COUP-TFI 表达升高所必需的。为了研究 COUP-TFI 在 RA 依赖性 P19 细胞分化过程中的作用,制备了可诱导表达不同水平 COUP-TFI 的 AS 细胞。AS 细胞中 COUP-TFI 的外源表达以剂量依赖性方式导致生长抑制、适度的细胞周期破坏和早期凋亡。此外,当表达药理学水平的 COUP-TFI 或同时表达生理水平的 COUP-TFI 和 RA 处理时,AS 细胞可以克服 RA 依赖性分化为内胚层细胞的阻断。此外,在表达 COUP-TFI 的 AS 细胞中,几种多能性相关基因(包括 OCT-4、DAX-1 和 SF-1)的 mRNA 水平降低。此外,对初级 RA 反应基因表达的分析表明,COUP-TFI 参与至少两个基因(CYP26A1 和 HoxA1)表达的调节调节。这些研究表明,COUP-TFI 在 RA 介导的 P19 细胞内胚层分化过程中作为一种生理相关的调节剂发挥作用。

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