首页> 外文期刊>Infection and immunity >Ehrlichia chaffeensis and E. sennetsu, but Not the Human Granulocytic Ehrlichiosis Agent, Colocalize with Transferrin Receptor and Up-Regulate Transferrin Receptor mRNA by Activating Iron-Responsive Protein 1
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Ehrlichia chaffeensis and E. sennetsu, but Not the Human Granulocytic Ehrlichiosis Agent, Colocalize with Transferrin Receptor and Up-Regulate Transferrin Receptor mRNA by Activating Iron-Responsive Protein 1

机译:Chaffeensis和E.sennetsu,但不是人类粒细胞埃希氏病病原体,与转铁蛋白受体共定位,并通过激活铁反应蛋白1上调转铁蛋白受体mRNA。

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Ehrlichia chaffeensis and E. sennetsu are genetically divergent obligatory intracellular bacteria of human monocytes and macrophages, and the human granulocytic ehrlichiosis (HGE) agent is an obligatory intracellular bacterium of granulocytes. Infection with both E. chaffeensis and E. sennetsu, but not HGE agent, in the acute monocytic leukemia cell line THP-1 almost completely inhibited by treatment with deferoxamine, a cell-permeable iron chelator. Transferrin receptors (TfRs) accumulated on both E. chaffeensis and E. sennetsu, but not HGE agent, inclusions in THP-1 cells or the cells of the promyelocytic leukemia cell line HL-60. Reverse transcription-PCR showed an increase in the level of TfR mRNA 6 h postinfection which peaked at 24 h postinfection with bothE. chaffeensis and E. sennetsu infection in THP-1 or HL-60 cells. In contrast, HGE agent in THP-1 or HL-60 cells induced no increase in TfR mRNA levels. Heat treatment of E. chaffeensis or the addition of monodansylcadaverine, a transglutaminase inhibitor, 3 h prior to infection inhibited the up-regulation of TfR mRNA. The addition of oxytetracycline 6 h after E. chaffeensis infection caused a decrease in TfR mRNA which returned to the basal level by 24 h postinfection. These results indicate that both internalization and continuous proliferation of ehrlichial organisms or the production of ehrlichial proteins are required for the up-regulation of TfR mRNA. Results of electrophoretic mobility shift assays showed that both E. chaffeensis and E. sennetsu infection increased the binding activity of iron-responsive protein 1 (IRP-1) to the iron-responsive element at 6 h postinfection and remained elevated at 24 h postinfection. However, HGE agent infection had no effect on IRP-1 binding activity. This result suggests that activation of IRP-1 and subsequent stabilization of TfR mRNA comprise the mechanism of TfR mRNA up-regulation by E. chaffeensis and E. sennetsu infection.
机译:恰菲埃里希氏菌 E。 sennetsu 是人类单核细胞和巨噬细胞的遗传异质性必需细胞内细菌,而人类粒细胞性埃希氏菌病(HGE)剂是粒状细胞的必需细胞内细菌。都感染了 E。 chaffeensis E。 sennetsu ,而不是HGE试剂,在急性单核细胞白血病细胞THP-1中几乎可以通过细胞可渗透的铁螯合剂去铁胺处理而完全抑制。两个E上都积累了转铁蛋白受体(TfRs)。 chaffeensis E。在THP-1细胞或早幼粒细胞白血病细胞系HL-60的细胞中包含但不包含HGE试剂。逆转录PCR显示感染后6小时TfR mRNA的水平增加,在两种E均感染后24小时达到峰值。 chaffeensis E。 THP-1或HL-60细胞感染sennetsu 。相比之下,THP-1或HL-60细胞中的HGE剂不会诱导TfR mRNA水平增加。 E的热处理。 Chaffeensis 或转谷氨酰胺酶抑制剂monodansylcadaverine的添加,在感染前3小时抑制了TfR mRNA的上调。 E后6小时加入土霉素。 Chaffeensis 感染引起TfR mRNA的下降,并在感染后24小时恢复到基础水平。这些结果表明,TfR mRNA的上调既需要内在微生物的内在化和持续增殖,又需要生产蛋白质。电泳迁移率变动分析的结果表明,两个E。 chaffeensis E。 sennetsu 感染在感染后6 h增加了铁反应蛋白1(IRP-1)与铁反应元件的结合活性,并在感染后24 h保持升高。但是,HGE试剂感染对IRP-1结合活性没有影响。该结果表明IRP-1的激活和随后TfR mRNA的稳定化构成了由 E上调TfR mRNA的机制。 chaffeensis E。 sennetsu 感染。

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