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鉴定负责12-氧十四烷酰佛波醇-13-乙酸酯(TPA)介导的髓单核细胞系中血红素加氧酶表达诱导的顺式调节元件和假定的反式作用因子。

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.

作者信息

Muraosa Y, Shibahara S

机构信息

Department of Applied Physiology and Molecular Biology, Tohoku University School of Medicine, Miyagi, Japan.

出版信息

Mol Cell Biol. 1993 Dec;13(12):7881-91. doi: 10.1128/mcb.13.12.7881-7891.1993.

Abstract

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.

摘要

人单核细胞白血病细胞系THP-1在用包括12-O-十四烷酰佛波醇-13-乙酸酯(TPA)在内的多种试剂处理时会分化为巨噬细胞样细胞。我们在此表明,在此过程中,血红素加氧酶(血红素分解代谢中的一种限速酶)的表达被诱导。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,但在其他谱系的细胞系(如HeLa细胞)中则不会。血红素加氧酶活性的增加可能代表活化巨噬细胞的功能之一,活化巨噬细胞会隔离衰老红细胞并降解源自血红蛋白的血红素。通过TPA处理的这种细胞类型特异性诱导作用,针对转录调控进行了进一步研究。我们确定了一个顺式调控元件5'-GTCATATGAC-3',它位于人血红素加氧酶基因的5'-侧翼区域(位置-156至-147),该元件赋予TPA在THP-1细胞中的诱导性,但在HeLa细胞中则没有。在THP-1核提取物中鉴定出与该元件结合的核蛋白,该元件可能是细胞特异性的原因。该元件包含共有基序CANNTG,一大类碱性螺旋-环-螺旋蛋白与之结合。我们的结果提示了TPA介导的骨髓单核细胞系转录调控的新机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f80b/364860/d1f07926e878/molcellb00024-0696-a.jpg

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