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人脐带间充质干细胞通过中枢和外周抑制 NLRP3 炎性小体介导体的炎性反应对 PD 小鼠发挥神经保护作用。

Neuroprotective effects of human umbilical cord mesenchymal stromal cells in PD mice via centrally and peripherally suppressing NLRP3 inflammasome-mediated inflammatory responses.

机构信息

Cell Therapy Center, Beijing Institute of Geriatrics, Xuanwu Hospital Capital Medical University, National Clinical Research Center for Geriatric Diseases, and Key Laboratory of Neurodegenerative Diseases, Ministry of Education, Beijing, China.

Cell Therapy Center, Beijing Institute of Geriatrics, Xuanwu Hospital Capital Medical University, National Clinical Research Center for Geriatric Diseases, and Key Laboratory of Neurodegenerative Diseases, Ministry of Education, Beijing, China; Center of Neural Injury and Repair, Beijing Institute for Brain Disorders, Beijing 100069, China; Center of Parkinson's Disease, Beijing Institute for Brain Disorders, Beijing 100069, China.

出版信息

Biomed Pharmacother. 2022 Sep;153:113535. doi: 10.1016/j.biopha.2022.113535. Epub 2022 Aug 12.

Abstract

Mesenchymal stromal cells (MSCs) exhibit beneficial anti-inflammatory effects against Parkinson's disease (PD) via immunomodulatory actions. However, the underlying molecular mechanism remains unclear. This study aimed to investigate the potential neuroprotective effects of MSCs and the possible mechanisms involved by infusing human umbilical cord MSCs (hMSCs) in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-treated mature male C57BL/6 mice. Subsequently, the striatal content of dopamine (DA) and its metabolites, tyrosine hydroxylase (TH)-positive neurons and activated microglia, circulating inflammatory cytokines, gene expression of cytokines, and NOD-like receptor protein 3 (NLRP3) inflammasome molecules were measured using high-performance liquid chromatography, flow cytometry, immunohistochemistry, immunofluorescent staining, and real-time polymerase chain reaction assays, respectively. Infused hMSCs markedly ameliorated the reduction in striatal DA and loss of TH-positive neurons in the substantia nigra of PD mice. The MPTP-induced activation of microglia and increase in tumor necrosis factor-α and interleukin-1β mRNA expression in the striatum were also attenuated by hMSCs. Furthermore, hMSCs completely reversed the elevated pro-inflammatory cytokine levels in the serum and mRNA expression of cytokines in the peripheral organs of PD mice. Moreover, hMSCs significantly inhibited the expression of caspase-1 and NLRP3 of the NLRP3 inflammasome in both the central and peripheral organs at mRNA level. These data suggest that hMSCs protect dopaminergic neurons in PD mice by suppressing both the central and peripheral inflammatory responses, probably by inhibiting the NLRP3 inflammasome. However, the animals in our study only received several MSC infusions, and the effects of infused MSCs over extended periods on the NLRP3 inflammasome need to be investigated in future studies.

摘要

间充质基质细胞 (MSCs) 通过免疫调节作用对帕金森病 (PD) 表现出有益的抗炎作用。然而,其潜在的分子机制尚不清楚。本研究旨在通过向 1-甲基-4-苯基-1,2,3,6-四氢吡啶 (MPTP) 处理的成熟雄性 C57BL/6 小鼠中输注人脐带 MSCs (hMSCs) 来研究 MSCs 的潜在神经保护作用及其可能涉及的机制。随后,使用高效液相色谱法、流式细胞术、免疫组织化学、免疫荧光染色和实时聚合酶链反应分别测定纹状体多巴胺 (DA) 及其代谢物、酪氨酸羟化酶 (TH)-阳性神经元和激活的小胶质细胞、循环炎症细胞因子、细胞因子的基因表达和 NOD 样受体蛋白 3 (NLRP3) 炎性体分子的含量。输注的 hMSCs 显著改善了 PD 小鼠纹状体 DA 的减少和黑质中 TH-阳性神经元的丢失。MPTP 诱导的小胶质细胞活化和纹状体中肿瘤坏死因子-α和白细胞介素-1β mRNA 表达的增加也被 hMSCs 减弱。此外,hMSCs 完全逆转了 PD 小鼠血清中促炎细胞因子水平和外周器官中细胞因子的 mRNA 表达的升高。此外,hMSCs 还显著抑制了中央和外周器官中 NLRP3 炎性体的 caspase-1 和 NLRP3 的 mRNA 表达。这些数据表明,hMSCs 通过抑制中枢和外周炎症反应来保护 PD 小鼠中的多巴胺能神经元,可能通过抑制 NLRP3 炎性体。然而,我们研究中的动物仅接受了几次 MSC 输注,需要在未来的研究中进一步探讨输注的 MSCs 在延长时间内对 NLRP3 炎性体的影响。

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