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Myeloid Dendritic Cells are Potential Players in Human Neurodegenerative Diseases

机译:髓样树突状细胞是人类神经退行性疾病的潜在参与者

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摘要

Alzheimer’s diseases (AD) and Parkinson’s diseases (PD) are devastating neurodegenerative disturbances, wherein neuroinflammation is a chronic pathogenic process with high therapeutic potential. Major mediators of AD/PD neuroimmune processes are resident immune cells, but immune cells derived from periphery may also participate and to some extent modify neuroinflammation. Specifically, blood borne myeloid cells emerge as crucial components of AD/PD progression and susceptibility. Among these, dendritic cells (DCs) are key immune orchestrators and players of brain immune surveillance; we candidate them as potential mediators of both AD and PD and as relevant cell model for unraveling myeloid cell role in neurodegeneration. Hence, we recapitulate and discuss emerging data suggesting that blood-derived DCs play a role in experimental and human neurodegenerative diseases. In humans, in particular, DCs are modified by in vitro culture with neurodegeneration-associated pathogenic factors and dysregulated in AD patients, while the levels of DC precursors are decreased in AD and PD patients’ blood, possibly as an index of their recruitment to the brain. Overall, we emphasize the need to explore the impact of DCs on neurodegeneration to uncover peripheral immune mechanisms of pathogenic importance, recognize potential biomarkers, and improve therapeutic approaches for neurodegenerative diseases.
机译:阿尔茨海默氏病(AD)和帕金森氏病(PD)是毁灭性的神经退行性疾病,其中神经炎症是具有高治疗潜力的慢性致病过程。 AD / PD神经免疫过程的主要介质是驻留的免疫细胞,但来源于外周的免疫细胞也可能参与并在一定程度上改变神经炎症。具体而言,血源性骨髓细胞是AD / PD进展和易感性的重要组成部分。其中,树突状细胞(DC)是关键的免疫协调器和脑部免疫监视的参与者。我们选择它们作为AD和PD的潜在介体,并作为揭示神经变性中髓样细胞作用的相关细胞模型。因此,我们总结并讨论了新兴数据,这些数据表明血液来源的DC在实验性和人类神经退行性疾病中起作用。特别是在人类中,DC通过与神经退行性疾病相关的致病因素的体外培养而被修饰,并在AD患者中失调,而AD和PD患者血液中DC前体的水平降低,这可能是其招募到DC的指标。脑。总体而言,我们强调需要探索DC对神经退行性疾病的影响,以发现具有致病性的外周免疫机制,识别潜在的生物标志物,并改善神经退行性疾病的治疗方法。

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