Do Bacterial Outer Membrane Vesicles Contribute to Chronic Inflammation in Parkinson's Disease?

IF 4 3区 医学 Q2 NEUROSCIENCES
Tiana F Koukoulis, Leah C Beauchamp, Maria Kaparakis-Liaskos, Rachel M McQuade, Adityas Purnianto, David I Finkelstein, Kevin J Barnham, Laura J Vella
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Abstract

Parkinson's disease (PD) is an increasingly common neurodegenerative disease. It has been suggested that the etiology of idiopathic PD is complex and multifactorial involving environmental contributions, such as viral or bacterial infections and microbial dysbiosis, in genetically predisposed individuals. With advances in our understanding of the gut-brain axis, there is increasing evidence that the intestinal microbiota and the mammalian immune system functionally interact. Recent findings suggest that a shift in the gut microbiome to a pro-inflammatory phenotype may play a role in PD onset and progression. While there are links between gut bacteria, inflammation, and PD, the bacterial products involved and how they traverse the gut lumen and distribute systemically to trigger inflammation are ill-defined. Mechanisms emerging in other research fields point to a role for small, inherently stable vesicles released by Gram-negative bacteria, called outer membrane vesicles in disease pathogenesis. These vesicles facilitate communication between bacteria and the host and can shuttle bacterial toxins and virulence factors around the body to elicit an immune response in local and distant organs. In this perspective article, we hypothesize a role for bacterial outer membrane vesicles in PD pathogenesis. We present evidence suggesting that these outer membrane vesicles specifically from Gram-negative bacteria could potentially contribute to PD by traversing the gut lumen to trigger local, systemic, and neuroinflammation. This perspective aims to facilitate a discussion on outer membrane vesicles in PD and encourage research in the area, with the goal of developing strategies for the prevention and treatment of the disease.

细菌外膜小泡是帕金森病慢性炎症的诱因吗?
帕金森病(PD)是一种日益常见的神经退行性疾病。有观点认为,特发性帕金森病的病因复杂且多因素,涉及环境因素,如病毒或细菌感染以及遗传易感个体的微生物菌群失调。随着我们对肠道-大脑轴的认识不断深入,越来越多的证据表明,肠道微生物群和哺乳动物免疫系统在功能上是相互影响的。最近的研究结果表明,肠道微生物群向促炎表型的转变可能在帕金森病的发病和进展中起作用。虽然肠道细菌、炎症和帕金森病之间存在联系,但所涉及的细菌产物及其如何穿过肠腔并分布到全身以引发炎症的机制尚不明确。其他研究领域出现的机制表明,革兰氏阴性细菌释放的固有稳定的小囊泡(称为外膜囊泡)在疾病发病机制中发挥作用。这些囊泡能促进细菌与宿主之间的交流,并能将细菌毒素和毒力因子穿梭于身体各处,从而引起局部和远处器官的免疫反应。在这篇透视文章中,我们假设细菌外膜囊泡在脓毒症发病机制中的作用。我们提出的证据表明,这些专门来自革兰氏阴性细菌的外膜囊泡有可能通过穿越肠腔引发局部、全身和神经炎症,从而导致帕金森病。这一观点旨在促进对帕金森病外膜囊泡的讨论,并鼓励该领域的研究,从而制定预防和治疗该疾病的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.40
自引率
5.80%
发文量
338
审稿时长
>12 weeks
期刊介绍: The Journal of Parkinson''s Disease (JPD) publishes original research in basic science, translational research and clinical medicine in Parkinson’s disease in cooperation with the Journal of Alzheimer''s Disease. It features a first class Editorial Board and provides rigorous peer review and rapid online publication.
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