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镉诱导的血红素加氧酶-1 基因表达与 Medicago sativa 根中谷胱甘肽的耗竭有关。

Cadmium-induced heme oxygenase-1 gene expression is associated with the depletion of glutathione in the roots of Medicago sativa.

机构信息

College of Life Sciences, Cooperative Demonstration Laboratory of Centrifuge Technique, Nanjing Agricultural University, Nanjing 210095, People's Republic of China.

出版信息

Biometals. 2011 Feb;24(1):93-103. doi: 10.1007/s10534-010-9377-2. Epub 2010 Sep 16.

DOI:10.1007/s10534-010-9377-2
PMID:20844928
Abstract

Following previous findings that cadmium (Cd) induces heme oxygenase-1 (HO1) gene expression in alfalfa seedling roots, we now show that the decreased glutathione (GSH) and ascorbic acid (AsA) contents, induction of HO-1 gene expression and its protein level by Cd was mimicked by a GSH depletor diethylmaleate (DEM). Meanwhile, above Cd- or DEM-induced decreased GSH content followed by HO-1 up-regulation could be strengthened or reversed differentially by the application of a selective inhibitor of GSH biosynthesis L: -buthionine-sulfoximine (BSO), or exogenous GSH and AsA, respectively. The antioxidative behavior of HO-1 induction was further confirmed by histochemical staining for the detection of loss of membrane integrity in a short period of treatment time. Additionally, the induction of HO-1 transcript was inhibited by the transcriptional inhibitor actinomycin D (ActD) or protein synthesis inhibitor cycloheximide (CX, especially). In contrast, the level of HO-2 transcript did not change upon various treatments. Together, above results suggested that Cd-induced up-regulation of HO-1 gene expression is associated with GSH depletion, which is at least existing transcriptional regulation level, thus leading to enhanced antioxidative capability transiently.

摘要

在先前的研究发现镉 (Cd) 诱导紫花苜蓿幼苗根中血红素加氧酶-1 (HO1) 基因表达后,我们现在表明,谷胱甘肽 (GSH) 和抗坏血酸 (AsA) 含量的降低、HO-1 基因表达的诱导及其蛋白水平由 Cd 模拟 GSH 耗竭剂马来酸二乙酯 (DEM)。同时,Cd 或 DEM 诱导的 GSH 含量降低后 HO-1 的上调可以通过 GSH 生物合成的选择性抑制剂 L: - 丁硫氨酸亚砜 (BSO) 、外源性 GSH 和 AsA 的应用分别得到增强或逆转。HO-1 诱导的抗氧化作用通过在短时间处理过程中检测膜完整性丧失的组织化学染色进一步得到证实。此外,转录抑制剂放线菌素 D (ActD) 或蛋白合成抑制剂环己酰亚胺 (CX,特别是) 抑制 HO-1 转录物的诱导。相比之下,各种处理对 HO-2 转录物的水平没有影响。综上所述,以上结果表明,Cd 诱导的 HO-1 基因表达上调与 GSH 耗竭有关,至少存在转录调控水平,从而导致短暂增强抗氧化能力。

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