...
首页> 外文期刊>Animal Cells and Systems >Phenotypic differences between Drosophila Alzheimer’s disease models expressing human Aβ42 in the developing eye and brain
【24h】

Phenotypic differences between Drosophila Alzheimer’s disease models expressing human Aβ42 in the developing eye and brain

机译:果蝇阿尔茨海默氏病模型在发育中的眼睛和大脑中表达人类Aβ42的表型差异

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Drosophila melanogaster expressing amyloid-β42 (Aβ42 ) transgenes have been used as models to study Alzheimer’s disease. Various Aβ42 transgenes with different structures induce different phenotypes, which make it difficult to compare data among studies which use different transgenic lines. In this study, we compared the phenotypes of four frequently used Aβ42 transgenic lines, UAS-Aβ42~(2X) , UAS-Aβ42~(BL33770) , UAS-Aβ42~(11C39) , and UAS-Aβ42~(H29.3) . Among the four transgenic lines, only UAS-Aβ42~(2X) has two copies of the upstream activation sequence-amyloid-β42 (UAS-Aβ42 ) transgene, while remaining three have one copy. UAS-Aβ42~(BL33770) has the 3′ untranslated region of Drosophila α-tubulin , while the others have that of SV40. UAS-Aβ42~(11C39) and UAS-Aβ42~(H29.3) have the rat pre-proenkephalin signal peptide, while UAS-Aβ42~(2X) and UAS-Aβ42~(BL33770) have that of the fly argos protein. When the transgenes were expressed ectopically in the developing eyes of the flies, UAS-Aβ42~(2X) transgene resulted in a strongly reduced and rough eye phenotype, while UAS-Aβ42~(BL33770) only showed a strong rough eye phenotype; UAS-Aβ42~(H29.3) and UAS-Aβ42~(11C39) had mild rough eyes. The levels of cell death and reactive oxygen species (ROS) in the eye imaginal discs were consistently the highest in UAS-Aβ42~(2X) , followed by UAS-Aβ42~(BL33770) , UAS-Aβ42~(11C39) , and UAS-Aβ42~(H29.3) . Surprisingly, the reduction in survival during the development of these lines did not correlate with cell death or ROS levels. The flies which expressed UAS-Aβ42~(11C39) or UAS-Aβ42~(H29.3) experienced greatly reduced survival rates, although low levels of ROS or cell death were detected. Collectively, our results demonstrated that different Drosophila AD models show different phenotypic severity, and suggested that different transgenes may have different modes of cytotoxicity.Abbreviations: Aβ42: amyloid-β42; AD: Alzheimer’s disease; UAS: upstream activation sequence.
机译:表达淀粉样蛋白-β42(Aβ42)转基因的果蝇已被用作研究阿尔茨海默氏病的模型。具有不同结构的各种Aβ42转基因诱导不同的表型,这使得在使用不同转基因系的研究之间难以比较数据。在这项研究中,我们比较了四种常用的Aβ42转基因系,UAS-Aβ42〜(2X),UAS-Aβ42〜(BL33770),UAS-Aβ42〜(11C39)的表型)和UAS-Aβ42〜(H29.3)。在这四个转基因品系中,仅UAS-Aβ42〜(2X)具有两个拷贝的上游激活序列-淀粉样-β42(UAS-Aβ42)转基因,而其余三个具有一个拷贝。 UAS-Aβ42〜(BL33770)具有果蝇α-微管蛋白的3'非翻译区,而其他具有SV40。 UAS-Aβ42〜(11C39)和UAS-Aβ42〜(H29.3)具有大鼠前脑啡肽原信号肽,而UAS-Aβ42〜(2X)和UAS-Aβ42 〜(BL33770)具有蝇果糖蛋白。当转基因在果蝇发育的眼睛中异位表达时,UAS-Aβ42〜(2X)转基因导致强烈的眼表型降低和粗糙,而UAS-Aβ42〜(BL33770)仅表现出强的眼表型眼表粗糙UAS-Aβ42〜(H29.3)和UAS-Aβ42〜(11C39)眼睛温和粗糙。眼部视盘中的细胞死亡和活性氧水平(ROS)在UAS-Aβ42〜(2X)中始终是最高的,其次是UAS-Aβ42〜(BL33770), UAS -Aβ42〜(11C39)和UAS-Aβ42〜(H29.3)。出人意料的是,这些细胞系发育过程中存活率的降低与细胞死亡或ROS水平无关。尽管检测到低水平的ROS或细胞死亡,但表达UAS-Aβ42〜(11C39)或UAS-Aβ42〜(H29.3)的果蝇的存活率大大降低。总体而言,我们的结果表明,不同的果蝇AD模型表现出不同的表型严重性,并表明不同的转基因可能具有不同的细胞毒性模式。广告:阿尔茨海默氏病; UAS:上游激活序列。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号