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类视黄醇受体RARα和RXRα的激活分别诱导HL-60细胞分化和凋亡。

Activation of retinoid receptors RAR alpha and RXR alpha induces differentiation and apoptosis, respectively, in HL-60 cells.

作者信息

Mehta K, McQueen T, Neamati N, Collins S, Andreeff M

机构信息

Department of Bioimmunotherapy, University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.

出版信息

Cell Growth Differ. 1996 Feb;7(2):179-86.

PMID:8822201
Abstract

Induction of granulocytic differentiation in HL-60 myeloid leukemia cells by retinoids is followed by their death via apoptosis. Retinoids are known to mediate their biological effects through at least two distinct types of nuclear receptors, the retinoic acid receptors and retinoid X receptors. We undertook to characterize the potential role of these receptors in inducing differentiation and apoptosis by retinoids. For this, we used a previously described variant of an HL-60 cell line (HL-60R) in which retinoid receptor function has been abrogated due to a trans-dominant negative mutation. Retroviral vector-mediated gene transfer was used to introduce the normal retinoic acid receptor (RAR alpha) or retinoid X receptor (RXR alpha) into HL-60R cells. Our results suggest that ligand-induced activation of RAR alpha is sufficient to induce differentiation in HL-60 cells, whereas activation of RXR alpha can induce direct apoptosis of these cells without their prior commitment to differentiate.

摘要

维甲酸可诱导HL-60髓系白血病细胞向粒细胞分化,随后这些细胞通过凋亡死亡。已知维甲酸通过至少两种不同类型的核受体介导其生物学效应,即维甲酸受体和维甲酸X受体。我们试图确定这些受体在维甲酸诱导分化和凋亡中的潜在作用。为此,我们使用了先前描述的HL-60细胞系变体(HL-60R),其中由于反式显性负突变,维甲酸受体功能已被废除。利用逆转录病毒载体介导的基因转移将正常的维甲酸受体(RARα)或维甲酸X受体(RXRα)导入HL-60R细胞。我们的结果表明,配体诱导的RARα激活足以诱导HL-60细胞分化,而RXRα的激活可诱导这些细胞直接凋亡,而无需它们事先承诺分化。

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