在黑质突触核蛋白病大鼠模型中,调节大麻素受体2可改变神经炎症并减少α-突触核蛋白聚集体的形成。

IF 9.3 1区 医学 Q1 IMMUNOLOGY
Valerie Joers, Benjamin C Murray, Caroline McLaughlin, Danielle Oliver, Hannah E Staley, Jazmyn Coronado, Cindy Achat-Mendes, Sanam Golshani, Sean D Kelly, Matthew Goodson, Danica Lee, Fredric P Manfredsson, Bob M Moore Ii, Malú Gámez Tansey
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引用次数: 0

摘要

对小胶质细胞表型失衡的研究已成为神经退行性疾病领域的一个焦点,因为它是导致帕金森病(PD)中慢性神经炎症和神经元丢失的潜在机制。越来越多的证据表明,神经炎症伴随并可能促进α-突触核蛋白(Asyn)诱导的黑质多巴胺能(DA)变性的进展。从治疗的角度来看,开发免疫调节策略,抑制长期激活的免疫细胞过度产生促炎细胞因子,并诱导促吞噬表型,有望促进Asyn的清除,保护脆弱的神经元。大麻素受体-2(CB2)在活化的小胶质细胞和外周免疫细胞上高度表达,在帕金森病患者的黑质和黑质变性小鼠模型中上调。此外,对 CB2 的调节可防止鱼藤酮诱导的黑质变性;然而,CB2 还没有在帕金森病的 Asyn 模型中被药理学选择性地靶向。我们在此报告,与药物治疗相比,外周给药 7 周的 CB2 逆激动剂 SMM-189 可减少黑质中磷酸化(pSer129)的 Asyn。此外,通过流式细胞术测定,SMM-189 还能延缓 Asyn 诱导的免疫细胞向大脑浸润,增加 CD68 蛋白表达,并提高伤口愈合免疫介导基因的表达。此外,外周免疫细胞增加了伤口愈合非典型单核细胞,减少了促炎性典型单核细胞。用脂多糖(LPS)和 SMM-189 处理 RAW264.7 巨噬细胞的体外分析表明,通过摄取 pHrodo 大肠杆菌生物颗粒的荧光测定,吞噬作用增强。这些结果表明,用 SMM-189 靶向 CB2 可使免疫细胞功能偏向吞噬表型,并减少 Asyn 的毒性聚集物种。我们的新发现表明,CB2 可能是调节蛋白病中炎症和免疫反应的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modulation of cannabinoid receptor 2 alters neuroinflammation and reduces formation of alpha-synuclein aggregates in a rat model of nigral synucleinopathy.

Research into the disequilibrium of microglial phenotypes has become an area of intense focus in neurodegenerative disease as a potential mechanism that contributes to chronic neuroinflammation and neuronal loss in Parkinson's disease (PD). There is growing evidence that neuroinflammation accompanies and may promote progression of alpha-synuclein (Asyn)-induced nigral dopaminergic (DA) degeneration. From a therapeutic perspective, development of immunomodulatory strategies that dampen overproduction of pro-inflammatory cytokines from chronically activated immune cells and induce a pro-phagocytic phenotype is expected to promote Asyn removal and protect vulnerable neurons. Cannabinoid receptor-2 (CB2) is highly expressed on activated microglia and peripheral immune cells, is upregulated in the substantia nigra of individuals with PD and in mouse models of nigral degeneration. Furthermore, modulation of CB2 protects against rotenone-induced nigral degeneration; however, CB2 has not been pharmacologically and selectively targeted in an Asyn model of PD. Here, we report that 7 weeks of peripheral administration of CB2 inverse agonist SMM-189 reduced phosphorylated (pSer129) Asyn in the substantia nigra compared to vehicle treatment. Additionally, SMM-189 delayed Asyn-induced immune cell infiltration into the brain as determined by flow cytometry, increased CD68 protein expression, and elevated wound-healing-immune-mediator gene expression. Additionally, peripheral immune cells increased wound-healing non-classical monocytes and decreased pro-inflammatory classical monocytes. In vitro analysis of RAW264.7 macrophages treated with lipopolysaccharide (LPS) and SMM-189 revealed increased phagocytosis as measured by the uptake of fluorescence of pHrodo E. coli bioparticles. Together, results suggest that targeting CB2 with SMM-189 skews immune cell function toward a phagocytic phenotype and reduces toxic aggregated species of Asyn. Our novel findings demonstrate that CB2 may be a target to modulate inflammatory and immune responses in proteinopathies.

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来源期刊
Journal of Neuroinflammation
Journal of Neuroinflammation 医学-神经科学
CiteScore
15.90
自引率
3.20%
发文量
276
审稿时长
1 months
期刊介绍: The Journal of Neuroinflammation is a peer-reviewed, open access publication that emphasizes the interaction between the immune system, particularly the innate immune system, and the nervous system. It covers various aspects, including the involvement of CNS immune mediators like microglia and astrocytes, the cytokines and chemokines they produce, and the influence of peripheral neuro-immune interactions, T cells, monocytes, complement proteins, acute phase proteins, oxidative injury, and related molecular processes. Neuroinflammation is a rapidly expanding field that has significantly enhanced our knowledge of chronic neurological diseases. It attracts researchers from diverse disciplines such as pathology, biochemistry, molecular biology, genetics, clinical medicine, and epidemiology. Substantial contributions to this field have been made through studies involving populations, patients, postmortem tissues, animal models, and in vitro systems. The Journal of Neuroinflammation consolidates research that centers around common pathogenic processes. It serves as a platform for integrative reviews and commentaries in this field.
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