幼年 Tg2576 小鼠的实验性结肠炎会加速阿尔茨海默氏症样临床表型的出现。

IF 7.9 1区 医学 Q1 CLINICAL NEUROLOGY
Luca Lorenzini, Lorenzo Zanella, Michele Sannia, Vito Antonio Baldassarro, Marzia Moretti, Maura Cescatti, Corinne Quadalti, Simone Baldi, Gianluca Bartolucci, Leandro Di Gloria, Matteo Ramazzotti, Paolo Clavenzani, Anna Costanzini, Roberto De Giorgio, Amedeo Amedei, Laura Calzà, Luciana Giardino
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引用次数: 0

摘要

流行病学和临床前数据表明,全身炎症和神经炎症会影响散发性阿尔茨海默病(AD)的自然病程,而一些流行病学研究表明,患有炎症性肠病的患者AD发病率更高。在这项研究中,我们探讨了右旋糖酐硫酸钠(DSS)诱导的年轻无症状/斑前小鼠结肠炎是否会加重和/或预示 Tg2576(一种广泛使用的老年痴呆症小鼠模型)的年龄依赖性认知障碍。我们证实,在年轻的 Tg2576 小鼠中诱导 DSS 结肠炎会提前 Morris 水迷宫测试中学习和记忆缺陷的发病年龄。为了探索DSS结肠炎加速Tg2576小鼠认知能力下降的潜在机制,我们重点研究了肠道微生物群、全身炎症和神经炎症标志物。我们观察到,Tg2576 DSS动物的固着菌/类杆菌比例变化与老年Tg2576小鼠相当,这表明Tg2576 DSS小鼠的微生物群加速老化,而C57BL6 DSS小鼠没有观察到这种变化。我们还观察到,Tg2576 和 WT 小鼠早在 3 个月大时,即斑块沉积之前,就在几种炎症和神经炎症相关参数上存在显著差异,与未接受 DSS 治疗的 Tg2576 和 WT 小鼠相比,这种差异发展迅速(3 到 5.5 个月大)。具体而言,在诱导DSS结肠炎后,WT和Tg2576小鼠海马中炎症诱发的星形胶质细胞相关基因的表达水平呈现出截然不同的特征。实验组之间海马中的小胶质细胞特征没有发生变化,但在Tg2576与WT小鼠之间观察到胶质纤维酸性蛋白免疫活性降低。这一发现可能反映了一种萎缩性的 "功能丧失 "特征,DSS 进一步加剧了这一特征,因为在 DSS 中检测到 GFAP mRNA 表达水平下降。总之,我们认为,由 DSS 结肠炎诱发并涉及肠道-大脑轴的尚未确定的外周介质强调了年轻 Tg2576 小鼠中星形胶质细胞的 "功能缺失 "特征,从而导致突触形态和功能完整性受损,这是 AD 的早期征兆。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Experimental colitis in young Tg2576 mice accelerates the onset of an Alzheimer's-like clinical phenotype.

Systemic inflammation and neuroinflammation affect the natural course of the sporadic form of Alzheimer's disease (AD), as supported by epidemiological and preclinical data, and several epidemiological studies indicate a higher prevalence of AD in patients with inflammatory bowel disease. In this study, we explored whether colitis induced by dextran sulfate sodium (DSS) in young, presymptomatic/preplaque mice worsens and/or anticipates age-dependent cognitive impairment in Tg2576, a widely used mouse model of AD. We demonstrated that DSS colitis induced in young Tg2576 mice anticipates the onset age of learning and memory deficit in the Morris water maze test. To explore potential mechanisms behind the acceleration of cognitive decline in Tg2576 mice by DSS colitis, we focused on gut microbiota, systemic inflammation and neuroinflammation markers. We observed a Firmicutes/Bacteroidetes ratio change in Tg2576 DSS animals comparable to that of elderly Tg2576 mice, suggesting accelerated microbiota aging in Tg2576 DSS mice, a change not observed in C57BL6 DSS mice. We also observed substantial differences between Tg2576 and WT mice in several inflammation and neuroinflammation-related parameters as early as 3 months of age, well before plaque deposition, a picture which evolved rapidly (between 3 and 5.5 months of age) in contrast to Tg2576 and WT littermates not treated with DSS. In detail, following induction of DSS colitis, WT and Tg2576 mice exhibited contrasting features in the expression level of inflammation-evoked astrocyte-associated genes in the hippocampus. No changes in microglial features occurred in the hippocampus between the experimental groups, whereas a reduced glial fibrillary acidic protein immunoreactivity was observed in Tg2576 vs. WT mice. This finding may reflect an atrophic, "loss-of-function" profile, further exacerbated by DSS where a decreased of GFAP mRNA expression level was detected. In conclusion, we suggest that as-yet unidentified peripheral mediators evoked by DSS colitis and involving the gut-brain axis emphasize an astrocyte "loss-of-function" profile present in young Tg2576 mice, leading to impaired synaptic morphological and functional integrity as a very early sign of AD.

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来源期刊
Alzheimer's Research & Therapy
Alzheimer's Research & Therapy 医学-神经病学
CiteScore
13.10
自引率
3.30%
发文量
172
审稿时长
>12 weeks
期刊介绍: Alzheimer's Research & Therapy is an international peer-reviewed journal that focuses on translational research into Alzheimer's disease and other neurodegenerative diseases. It publishes open-access basic research, clinical trials, drug discovery and development studies, and epidemiologic studies. The journal also includes reviews, viewpoints, commentaries, debates, and reports. All articles published in Alzheimer's Research & Therapy are included in several reputable databases such as CAS, Current contents, DOAJ, Embase, Journal Citation Reports/Science Edition, MEDLINE, PubMed, PubMed Central, Science Citation Index Expanded (Web of Science) and Scopus.
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