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自发性突变频率在哈林顿氏小丑(hq)/Big Blue 老鼠的皮肤中升高。

Spontaneous mutation frequency is elevated in skin of harlequin (hq)/Big Blue mice.

机构信息

Department of Biology, The University of Western Ontario, Biological and Geological Sciences Building, 1151 Richmond Street North, London, Ontario, Canada.

出版信息

Mutagenesis. 2010 May;25(3):235-42. doi: 10.1093/mutage/gep069. Epub 2010 Jan 20.

Abstract

The harlequin (hq)/Big Blue mouse is a novel model of premature ageing distinguished by a patchy coat, early-onset neurodegeneration, stress-induced heart disease and a mutation detection assay applicable to individual tissues. The hq mutation causes down-regulation of apoptosis-inducing factor and an elevation of reactive oxygen species (ROS). Neural tissues have elevated mutant frequency and early-onset degeneration. This is the first examination of mutations and histology in the skin of hq disease mice. The frequency and pattern of cII mutations in skin from adult hq disease and wild-type (WT) mice 15 days after a single intraperitoneal (i.p.) injection of paraquat (PQ; 10 mg/kg) or vehicle control (VC) were determined to assess spontaneous mutagenesis and sensitivity to an exogenous ROS-inducing mutagen. Skin of hq disease mice shows elevated levels of ROS (P < 0.001) and reduced numbers of hair follicles and associated epidermal cells (P < 0.001) compared to WT control. Acute PQ exposure did not produce detectable skin histopathology. Spontaneous and PQ-induced mutation frequency is elevated in hq skin (P = 0.03 and P = 0.01, respectively) compared to VC-treated WT mice. Despite elevated mutation frequency, mutation patterns were unaltered. Acute PQ exposure resulted in a 1.6-fold increase in mutation frequency in WT mice compared to the level of spontaneous mutations but no significant impact on mutation frequency in hq disease mice. Increased mutation frequency in skin of hq disease mice may be relevant to mechanisms underlying the patchy coat and useful as a biomarker in tests of antioxidant efficacy in preventing the hq disease phenotype. Unaltered mutation patterns with hq disease are consistent with the multiple mutation types associated with ROS. Acute PQ exposure had only subtle effects in WT mice and reduced mitochondrial complex I activity and elevated antioxidant enzyme activity in hq disease mice may lead to PQ resistance.

摘要

花斑(hq)/大蓝鼠是一种新型的早衰模型,其特征为斑驳的被毛、早发性神经退行性变、应激诱导的心脏病以及适用于个体组织的突变检测分析。hq 突变导致凋亡诱导因子下调和活性氧(ROS)升高。神经组织的突变频率升高且早发性退化。这是首次对 hq 疾病小鼠皮肤中的突变和组织学进行检查。在单次腹腔内(i.p.)注射百草枯(PQ;10mg/kg)或载体对照(VC)后 15 天,测定 hq 疾病和野生型(WT)小鼠皮肤中 cII 突变的频率和模式,以评估自发突变和对外源 ROS 诱导诱变剂的敏感性。与 WT 对照相比,hq 疾病小鼠的皮肤显示出升高的 ROS 水平(P < 0.001)和减少的毛囊和相关表皮细胞数量(P < 0.001)。急性 PQ 暴露未产生可检测的皮肤组织病理学变化。与 VC 处理的 WT 小鼠相比,hq 皮肤中的自发和 PQ 诱导突变频率升高(分别为 P = 0.03 和 P = 0.01)。尽管突变频率升高,但突变模式未改变。与自发突变相比,急性 PQ 暴露使 WT 小鼠的突变频率增加了 1.6 倍,但对 hq 疾病小鼠的突变频率没有显著影响。hq 疾病小鼠皮肤中的突变频率增加可能与斑驳的被毛有关,并且可以作为测试抗氧化剂功效以预防 hq 疾病表型的生物标志物。hq 疾病的突变模式不变与 ROS 相关的多种突变类型一致。急性 PQ 暴露对 WT 小鼠仅有轻微影响,而 hq 疾病小鼠中减少的线粒体复合物 I 活性和升高的抗氧化酶活性可能导致 PQ 耐药性。

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