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口腔病原菌诱导人神经细胞平台中的神经退行性小胶质细胞激活

Oral Pathogenic Bacteria-Inducing Neurodegenerative Microgliosis in Human Neural Cell Platform.

机构信息

Department of Biophysics, Institute of Quantum Biophysics, Sungkyunkwan University, Suwon 16419, Korea.

Department of Intelligent Precision Healthcare Convergence, Institute of Quantum Biophysics, Sungkyunkwan University, Suwon 16419, Korea.

出版信息

Int J Mol Sci. 2021 Jun 28;22(13):6925. doi: 10.3390/ijms22136925.

Abstract

is a gram-negative bacterium found in the human oral cavity and is responsible for the development of chronic periodontitis as well as neurological diseases, including Alzheimer's disease (AD). Given the significance of the roles of in AD pathogenesis, it is critical to understand the underlying mechanisms of -driven neuroinflammation and their contribution to neurodegeneration. Herein, we hypothesize that produces secondary metabolites that may cause neurodegeneration through direct or indirect pathways mediated by microglia. To test our hypothesis, we treated human neural cells with bacterial conditioned media on our brain platforms and assessed microgliosis, astrogliosis and neurodegeneration. We found that bacteria-mediated microgliosis induced the production of nitric oxide, which causes neurodegeneration assessed with high pTau level. Our study demonstrated the elevation of detrimental protein mediators, CD86 and iNOS and the production of several pro-inflammatory markers from stimulated microglia. Through inhibition of LPS and succinate dehydrogenase in a bacterial conditioned medium, we showed a decrease in neurodegenerative microgliosis. In addition, we demonstrated the bidirectional effect of microgliosis and astrogliosis on each other exacerbating neurodegeneration. Overall, our study suggests that the mouth-brain axis may contribute to the pathogenesis of AD.

摘要

牙龈卟啉单胞菌是一种存在于人类口腔中的革兰氏阴性菌,它是导致慢性牙周炎和包括阿尔茨海默病(AD)在内的神经退行性疾病的罪魁祸首。鉴于在 AD 发病机制中发挥的重要作用,了解牙龈卟啉单胞菌驱动的神经炎症的潜在机制及其对神经退行性变的贡献至关重要。在此,我们假设牙龈卟啉单胞菌会产生可能通过小胶质细胞介导的直接或间接途径导致神经退行性变的次生代谢物。为了验证我们的假设,我们在脑平台上用人神经细胞的细菌条件培养基进行处理,并评估小胶质细胞增生、星形胶质细胞增生和神经退行性变。我们发现,细菌介导的小胶质细胞增生诱导了一氧化氮的产生,而高水平的 pTau 则表明其会导致神经退行性变。我们的研究表明,从受刺激的小胶质细胞中产生了有害的蛋白介质 CD86 和 iNOS 以及几种促炎标志物。通过抑制细菌条件培养基中的 LPS 和琥珀酸脱氢酶,我们发现神经退行性小胶质细胞增生减少。此外,我们还证明了小胶质细胞增生和星形胶质细胞增生之间的相互作用对神经退行性变具有双向影响。总的来说,我们的研究表明,口腔-大脑轴可能有助于 AD 的发病机制。

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