Impact of Mast Cell Activation on Neurodegeneration: A Potential Role for Gut-Brain Axis and Helicobacter pylori Infection.

IF 3.2 Q2 CLINICAL NEUROLOGY Neurology International Pub Date : 2024-12-06 DOI:10.3390/neurolint16060127
Marina Boziki, Paschalis Theotokis, Evangelia Kesidou, Maria Nella, Christos Bakirtzis, Eleni Karafoulidou, Maria Tzitiridou-Chatzopoulou, Michael Doulberis, Evangelos Kazakos, Georgia Deretzi, Nikolaos Grigoriadis, Jannis Kountouras
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Abstract

Background: The innate immune response aims to prevent pathogens from entering the organism and/or to facilitate pathogen clearance. Innate immune cells, such as macrophages, mast cells (MCs), natural killer cells and neutrophils, bear pattern recognition receptors and are thus able to recognize common molecular patterns, such as pathogen-associated molecular patterns (PAMPs), and damage-associated molecular patterns (DAMPs), the later occurring in the context of neuroinflammation. An inflammatory component in the pathology of otherwise "primary cerebrovascular and neurodegenerative" disease has recently been recognized and targeted as a means of therapeutic intervention. Activated MCs are multifunctional effector cells generated from hematopoietic stem cells that, together with dendritic cells, represent first-line immune defense mechanisms against pathogens and/or tissue destruction.

Methods: This review aims to summarize evidence of MC implication in the pathogenesis of neurodegenerative diseases, namely, Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, Huntington's disease, and multiple sclerosis.

Results: In view of recent evidence that the gut-brain axis may be implicated in the pathogenesis of neurodegenerative diseases and the characterization of the neuroinflammatory component in the pathology of these diseases, this review also focuses on MCs as potential mediators in the gut-brain axis bi-directional communication and the possible role of Helicobacter pylori, a gastric pathogen known to alter the gut-brain axis homeostasis towards local and systemic pro-inflammatory responses.

Conclusion: As MCs and Helicobacter pylori infection may offer targets of intervention with potential therapeutic implications for neurodegenerative disease, more clinical and translational evidence is needed to elucidate this field.

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肥大细胞活化对神经退行性变的影响:肠脑轴和幽门螺杆菌感染的潜在作用。
背景:先天免疫反应旨在阻止病原体进入机体和/或促进病原体清除。先天免疫细胞,如巨噬细胞、肥大细胞(MCs)、自然杀伤细胞和中性粒细胞,具有模式识别受体,因此能够识别常见的分子模式,如病原体相关分子模式(PAMPs)和损伤相关分子模式(DAMPs),后者发生在神经炎症的背景下。在“原发性脑血管和神经退行性”疾病的病理中,炎症成分最近被认识到并作为治疗干预的一种手段。活化的MCs是由造血干细胞产生的多功能效应细胞,与树突状细胞一起,代表了对抗病原体和/或组织破坏的一线免疫防御机制。方法:本综述旨在总结MC在神经退行性疾病,即阿尔茨海默病、帕金森病、肌萎缩侧索硬化症、亨廷顿病和多发性硬化症发病机制中的作用。结果:鉴于最近有证据表明肠-脑轴可能参与神经退行性疾病的发病机制以及这些疾病病理中神经炎症成分的表征,本文还将重点介绍MCs作为肠-脑轴双向通讯的潜在介质,以及幽门螺杆菌的可能作用,幽门螺杆菌是一种已知可以改变肠-脑轴稳态的胃病原体,导致局部和全身的促炎反应。结论:MCs和幽门螺杆菌感染可能是神经退行性疾病的干预靶点,具有潜在的治疗意义,需要更多的临床和转化证据来阐明这一领域。
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来源期刊
Neurology International
Neurology International CLINICAL NEUROLOGY-
CiteScore
3.70
自引率
3.30%
发文量
69
审稿时长
11 weeks
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