工程益生菌乳酸乳球菌MG1363-pMG36e-GLP-1调节帕金森病转基因小鼠模型中的小胶质细胞极化和肠道生态失调。

IF 6.7 2区 医学 Q2 CELL BIOLOGY
Neural Regeneration Research Pub Date : 2026-03-01 Epub Date: 2025-01-13 DOI:10.4103/NRR.NRR-D-24-00702
Mengyun Yue, Tingtao Chen, Wenjie Chen, Jing Wei, Bin Liao, Jie Zhang, Fangjun Li, Daojun Hong, Xin Fang
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引用次数: 0

摘要

帕金森病以突触核蛋白病相关神经退行性变为特征。先前的研究表明胰高血糖素样肽-1 (GLP-1)对1-甲基-4-苯基-1,2,3,6-四氢吡啶诱导的帕金森病小鼠模型有有益作用。然而,GLP-1对内在突触核蛋白功能障碍的影响尚不清楚。在本研究中,我们研究了乳酸乳球菌MG1363-pMG36e-GLP-1对SncaA53T转基因小鼠帕金森病的影响,并探讨其潜在机制。我们的数据显示,在SncaA53T转基因小鼠中,乳酸乳球菌MG1363-pMG36e-GLP-1抑制多巴胺能神经元死亡,减少α-突触核蛋白的病理性聚集,减少运动障碍。此外,乳酸乳球菌MG1363-pMG36e-GLP-1下调脂多糖相关炎症,降低大脑小胶质细胞和星形胶质细胞的激活,并通过黑质中GLP-1受体/PI3K/Akt通路促进细胞存活。此外,乳酸乳球菌MG1363-pMG36e-GLP-1降低血清中促炎分子的水平,包括脂多糖、脂多糖结合蛋白、白细胞介素-1β和白细胞介素-6。肠道组织病理学和western blotting进一步显示,乳酸乳球菌MG1363-pMG36e-GLP-1通过逆转SncaA53T转基因小鼠的肠道生态失调,增加肠道完整性相关蛋白的表达,减少脂多糖相关炎症。我们的研究结果表明,乳酸乳球菌MG1363-pMG36e-GLP-1对SncaA53T转基因小鼠帕金森病性状的有益作用是通过小胶质细胞极化和生态失调的逆转介导的。总之,我们的研究结果表明,乳酸乳球菌MG1363-pMG36e-GLP-1是治疗帕金森病的一种有前景的治疗剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The engineered probiotic strain Lactococcus lactis MG1363-pMG36e-GLP-1 regulates microglial polarization and gut dysbiosis in a transgenic mouse model of Parkinson's disease.

JOURNAL/nrgr/04.03/01300535-202603000-00044/figure1/v/2025-06-16T082406Z/r/image-tiff Parkinson's disease is characterized by synucleinopathy-associated neurodegeneration. Previous studies have shown that glucagon-like peptide-1 (GLP-1) has beneficial effects in a mouse model of Parkinson's disease induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine. However, the effect of GLP-1 on intrinsic synuclein malfunction remains unclear. In this study, we investigated the effect of Lactococcus lactis MG1363-pMG36e-GLP-1 on parkinsonism in SncaA53T transgenic mice and explored the underlying mechanisms. Our data showed that Lactococcus lactis MG1363-pMG36e-GLP-1 inhibited dopaminergic neuronal death, reduced pathological aggregation of α-synuclein, and decreased movement disorders in SncaA53T transgenic mice. Furthermore, Lactococcus lactis MG1363-pMG36e-GLP-1 downregulated lipopolysaccharide-related inflammation, reduced cerebral activation of microglia and astrocytes, and promoted cell survival via the GLP-1 receptor/PI3K/Akt pathway in the substantia nigra. Additionally, Lactococcus lactis MG1363-pMG36e-GLP-1 decreased serum levels of pro-inflammatory molecules including lipopolysaccharide, lipopolysaccharide binding protein, interleukin-1β, and interleukin-6. Gut histopathology and western blotting further revealed that Lactococcus lactis MG1363-pMG36e-GLP-1 increased the expression of gut integrity-related proteins and reduced lipopolysaccharide-related inflammation by reversing gut dysbiosis in SncaA53T transgenic mice. Our findings showed that the beneficial effect of Lactococcus lactis MG1363-pMG36e-GLP-1 on parkinsonism traits in SncaA53T transgenic mice is mediated by microglial polarization and the reversal of dysbiosis. Collectively, our findings suggest that Lactococcus lactis MG1363-pMG36e-GLP-1 is a promising therapeutic agent for the treatment of Parkinson's disease.

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来源期刊
Neural Regeneration Research
Neural Regeneration Research CELL BIOLOGY-NEUROSCIENCES
CiteScore
8.00
自引率
9.80%
发文量
515
审稿时长
1.0 months
期刊介绍: Neural Regeneration Research (NRR) is the Open Access journal specializing in neural regeneration and indexed by SCI-E and PubMed. The journal is committed to publishing articles on basic pathobiology of injury, repair and protection to the nervous system, while considering preclinical and clinical trials targeted at improving traumatically injuried patients and patients with neurodegenerative diseases.
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