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工程益生菌乳酸乳球菌MG1363-pMG36e-GLP-1在帕金森病转基因小鼠模型中调节小胶质细胞极化和肠道菌群失调。

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.

作者信息

Yue Mengyun, Chen Tingtao, Chen Wenjie, Wei Jing, Liao Bin, Zhang Jie, Li Fangjun, Hong Daojun, Fang Xin

机构信息

Department of Neurology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi Province, China.

National Engineering Research Center of Bioengineering Drugs and Technologies, Institute of Translational Medicine, Nanchang University, Nanchang, Jiangxi Province, China.

出版信息

Neural Regen Res. 2026 Mar 1;21(3):1211-1221. doi: 10.4103/NRR.NRR-D-24-00702. Epub 2025 Jan 13.

Abstract

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.

摘要

《期刊》/nrgr/04.03/01300535 - 202603000 - 00044/图1/v/2025 - 06 - 16T082406Z/图像 - tiff格式 帕金森病的特征是与突触核蛋白病相关的神经退行性变。先前的研究表明,胰高血糖素样肽 - 1(GLP - 1)在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中具有有益作用。然而,GLP - 1对内在突触核蛋白功能障碍的影响仍不清楚。在本研究中,我们研究了乳酸乳球菌MG1363 - pMG36e - GLP - 1对SncaA53T转基因小鼠帕金森症的影响,并探索其潜在机制。我们的数据表明,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,并减轻SncaA53T转基因小鼠的运动障碍。此外,乳酸乳球菌MG1363 - pMG36e - GLP - 1下调脂多糖相关炎症,减少黑质中小胶质细胞和星形胶质细胞的脑内激活,并通过GLP - 1受体/PI3K/Akt途径促进细胞存活。另外,乳酸乳球菌MG1363 - pMG36e - GLP - 1降低血清中包括脂多糖、脂多糖结合蛋白、白细胞介素 - 1β和白细胞介素 - 6在内的促炎分子水平。肠道组织病理学和蛋白质印迹进一步显示,乳酸乳球菌MG1363 - pMG36e - GLP - 1通过逆转SncaA53T转基因小鼠的肠道菌群失调增加肠道完整性相关蛋白的表达并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转基因小鼠帕金森症特征的有益作用是由小胶质细胞极化和菌群失调的逆转介导的。总体而言,我们的研究结果表明乳酸乳球菌MG1363 - pMG36e - GLP - 1是一种有前途的治疗帕金森病的药物。

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