Suppr超能文献

14 月龄雌性 TAU58/2 转基因小鼠的行为表型。

The behavioural phenotype of 14-month-old female TAU58/2 transgenic mice.

机构信息

School of Medicine, Western Sydney University, NSW 2560, Australia.

School of Medicine, Western Sydney University, NSW 2560, Australia; Faculty of Medical and Life Sciences, Hochschule Furtwangen University, 78054 Villingen-Schwenningen, Germany.

出版信息

Behav Brain Res. 2021 Jan 15;397:112943. doi: 10.1016/j.bbr.2020.112943. Epub 2020 Oct 2.

Abstract

Frontotemporal dementia (FTD) and Alzheimer's disease (AD) exhibit intracellular inclusions [neurofibrillary tangles (NFT's)] of microtubule-associated protein tau that contributes to neuronal dysfunction and death. Mutations in the microtubule-associated protein tau (MAPT) gene leads to tau hyperphosphorylation and promotes NFT formation. The TAU58/2 transgenic mouse model expresses mutant human tau (P301S mutation) and exhibits behavioural abnormalities relevant to dementia in early adulthood. Here we comprehensively determined the behavioural phenotype of TAU58/2 transgenic female mice at 14 months of age using test paradigms relevant to FTD and AD. TAU58/2 females showed a significant motor deficit and lower bodyweight compared to WT littermates. Transgenic females failed to habituate to the test arena in the light-dark test. Interestingly, transgenics did not exhibit an anxiolytic-like phenotype and intermediate-term spatial learning in the cheeseboard test was intact. However, a significant learning deficit was detected in the 1st trial across test days indicating impaired long-term spatial memory. In addition, the preference for a previously rewarded location was absent in transgenic females during probe trial testing. Finally, TAU58/2 mice had a defective acoustic startle response and impaired sensorimotor gating. In conclusion TAU58/2 mice exhibit several behavioural deficits that resemble those observed in human FTD and AD. Additionally, we observed a novel startle response deficit in these mice. At 14 months of age, TAU58/2 females represent a later disease stage and are therefore a potentially useful model to test efficacy of therapeutics to reverse or ameliorate behavioural deficits in post-onset tauopapthy-related neurodegenerative disorders.

摘要

额颞叶痴呆(FTD)和阿尔茨海默病(AD)表现为微管相关蛋白 tau 的细胞内包涵体[神经原纤维缠结(NFT)],导致神经元功能障碍和死亡。微管相关蛋白 tau(MAPT)基因突变导致 tau 过度磷酸化并促进 NFT 形成。TAU58/2 转基因小鼠模型表达突变型人 tau(P301S 突变),并表现出与成年早期痴呆相关的行为异常。在这里,我们使用与 FTD 和 AD 相关的测试范式,全面确定了 14 月龄 TAU58/2 转基因雌性小鼠的行为表型。与 WT 同窝仔相比,TAU58/2 雌性小鼠表现出明显的运动缺陷和体重下降。转基因雌性在明暗测试中未能适应测试场地。有趣的是,转基因小鼠没有表现出抗焦虑样表型,在奶酪板测试中也没有中间期空间学习能力受损。然而,在第 1 次试验中,在整个测试日中检测到明显的学习缺陷,表明长期空间记忆受损。此外,在探针试验测试中,转基因雌性对以前奖励位置的偏好消失。最后,TAU58/2 小鼠的听觉惊跳反应和感觉运动门控受损。总之,TAU58/2 小鼠表现出几种类似于人类 FTD 和 AD 观察到的行为缺陷。此外,我们在这些小鼠中观察到一种新的惊跳反应缺陷。在 14 月龄时,TAU58/2 雌性代表更晚期的疾病阶段,因此是测试治疗逆转或改善与 tau 相关的神经退行性疾病发病后行为缺陷疗效的潜在有用模型。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验