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RGS10减轻慢性炎症应激诱导的全身免疫失调。

RGS10 Attenuates Systemic Immune Dysregulation Induced by Chronic Inflammatory Stress.

作者信息

Jernigan Janna E, Staley Hannah A, Baty Zachary, Bolen MacKenzie L, Gomes Beatriz Nuñes, Holt Jenny, Cole Cassandra L, Neighbarger Noelle K, Dheeravath Kruthika, Merchak Andrea R, Menees Kelly B, Coombes Stephen A, Tansey Malú Gámez

机构信息

Center for Translational Research in Neurodegenerative Disease, College of Medicine, University of Florida, Gainesville, FL, USA.

Department of Neuroscience, College of Medicine, University of Florida, Gainesville, FL, USA.

出版信息

bioRxiv. 2024 Oct 29:2024.10.24.620078. doi: 10.1101/2024.10.24.620078.

Abstract

Regulator of G-protein signaling 10 (RGS10), a key homeostatic regulator of immune cells, has been implicated in multiple diseases associated with aging and chronic inflammation including Parkinson's Disease (PD). Interestingly, subjects with idiopathic PD display reduced levels of RGS10 in subsets of peripheral immune cells. Additionally, individuals with PD have been shown to have increased activated peripheral immune cells in cerebral spinal fluid (CSF) compared to age-matched healthy controls. However, it is unknown whether CSF-resident peripheral immune cells in individuals with PD also exhibit decreased levels of RGS10. Therefore, we performed an analysis of RGS10 levels in the proteomic database of the CSF from the Michael J. Fox Foundation Parkinson's Progression Markers Initiative (PPMI) study. We found that RGS10 levels are decreased in the CSF of individuals with PD compared to healthy controls and prodromal individuals. Moreover, we find that RGS10 levels decrease with age but not PD progression and that males have less RGS10 than females in PD. Importantly, studies have established an association between chronic systemic inflammation (CSI) and neurodegenerative diseases, such as PD, and known sources of CSI have been identified as risk factors for developing PD; however, the role of peripheral immune cell dysregulation in this process has been underexplored. As RGS10 levels are decreased in the CSF and circulating peripheral immune cells of individuals with PD, we hypothesized that RGS10 regulates peripheral immune cell responses to CSI prior to the onset of neurodegeneration. To test this, we induced CSI for 6 weeks in C57BL6/J mice and RGS10 KO mice to assess circulating and CNS-associated peripheral immune cell responses. We found that RGS10 deficiency synergizes with CSI to induce a bias for inflammatory and cytotoxic cell populations, a reduction in antigen presentation in peripheral blood immune cells, as well as in and around the brain that is most notable in males. These results highlight RGS10 as an important regulator of the systemic immune response to CSI and implicate RGS10 as a potential contributor to the development of immune dysregulation in PD.

摘要

G蛋白信号调节因子10(RGS10)是免疫细胞的关键稳态调节因子,与包括帕金森病(PD)在内的多种与衰老和慢性炎症相关的疾病有关。有趣的是,特发性PD患者外周免疫细胞亚群中的RGS10水平降低。此外,与年龄匹配的健康对照相比,PD患者脑脊液(CSF)中活化的外周免疫细胞增加。然而,PD患者脑脊液中驻留的外周免疫细胞RGS10水平是否也降低尚不清楚。因此,我们对迈克尔·J·福克斯基金会帕金森病进展标志物倡议(PPMI)研究的脑脊液蛋白质组数据库中的RGS10水平进行了分析。我们发现,与健康对照和前驱个体相比,PD患者脑脊液中的RGS10水平降低。此外,我们发现RGS10水平随年龄降低,但不随PD进展而降低,且PD男性患者的RGS10低于女性。重要的是,研究已证实慢性全身炎症(CSI)与神经退行性疾病如PD之间存在关联,且已知的CSI来源已被确定为PD发病的危险因素;然而,外周免疫细胞失调在这一过程中的作用尚未得到充分研究。由于PD患者脑脊液和循环外周免疫细胞中的RGS10水平降低,我们推测RGS10在神经退行性变发生之前调节外周免疫细胞对CSI的反应。为了验证这一点,我们在C57BL6/J小鼠和RGS10基因敲除小鼠中诱导CSI 6周,以评估循环和中枢神经系统相关外周免疫细胞的反应。我们发现,RGS10缺乏与CSI协同作用,诱导炎症和细胞毒性细胞群体偏向,外周血免疫细胞以及大脑内外的抗原呈递减少,这在男性中最为明显。这些结果突出了RGS10作为对CSI全身免疫反应的重要调节因子,并表明RGS10可能是PD免疫失调发展的一个促成因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb4/11566001/2f9ef88500cb/nihpp-2024.10.24.620078v1-f0001.jpg

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