首页> 美国卫生研究院文献>Molecular and Cellular Biology >Identification of a cis-regulatory element and putative trans-acting factors responsible for 12-O-tetradecanoylphorbol-13-acetate (TPA)-mediated induction of heme oxygenase expression in myelomonocytic cell lines.
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Identification of a cis-regulatory element and putative trans-acting factors responsible for 12-O-tetradecanoylphorbol-13-acetate (TPA)-mediated induction of heme oxygenase expression in myelomonocytic cell lines.

机译:负责顺式调控元件和推定的反式作用因子的鉴定所述顺式调控元件和推定的反式作用因子负责骨髓单核细胞系中12-O-十四烷酰phorbol-13-乙酸盐(TPA)介导的血红素加氧酶表达诱导。

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摘要

The human monocytic leukemia cell line THP-1 differentiates into macrophage-like cells when treated with a variety of agents, including 12-O-tetradecanoylphorbol-13-acetate (TPA). We show here that during this process, the expression of heme oxygenase, a rate-limiting enzyme in heme catabolism, is induced. Treatment with TPA increases heme oxygenase mRNA in other myelomonocytic cell lines also, but not in cell lines of other lineages, such as HeLa cells. Increased heme oxygenase activity may represent one of the functions of activated macrophages, which sequestrate senescent erythrocytes and degrade heme derived from hemoglobin. This cell-type-specific induction by TPA treatment further investigated with respect to transcriptional regulation. We defined a cis-regulatory element, 5'-GTCATATGAC-3', located in the 5'-flanking region (positions -156 to -147) of the human heme oxygenase gene, which confers inducibility by TPA in THP-1 cells but not in HeLa cells. Nuclear proteins that bind to this element, which may be responsible for the cell specificity, were identified in THP-1 nuclear extracts. This element contains the consensus motif CANNTG, to which a large family of basic helix-loop-helix proteins binds. Our results suggest a novel mechanism of TPA-mediated transcriptional regulation in myelomonocytic cell lines.
机译:人单核细胞白血病细胞系THP-1经过多种试剂(包括12-O-十四烷酰佛波醇13-乙酸酯(TPA))处理后,分化为巨噬细胞样细胞。我们在这里显示,在此过程中,血红素加氧酶的表达,一种在血红素分解代谢中的限速酶被诱导。用TPA处理也会增加其他骨髓单核细胞系中的血红素加氧酶mRNA,但不会增加其他谱系(例如HeLa细胞)中的血红素加氧酶mRNA。血红素加氧酶活性的提高可能代表了活化的巨噬细胞的功能之一,该巨噬细胞螯合衰老的红细胞并降解源自血红蛋白的血红素。 TPA处理的这种细胞类型特异性诱导作用在转录调控方面作了进一步研究。我们定义了一个顺式调控元件5'-GTCATATGAC-3',位于人类血红素加氧酶基因的5'侧翼区域(-156至-147位),赋予TPA在THP-1细胞中诱导性,但不在HeLa细胞中。在THP-1核提取物中鉴定出与该元素结合的核蛋白,这可能是造成细胞特异性的原因。该元素包含共有基序CANNTG,大家族的基本螺旋-环-螺旋蛋白与之结合。我们的结果表明TPA介导的骨髓单核细胞系中的转录调控的新机制。

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