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个人简介

教育背景 2012.10-2016.3 九州大学,齿学研究院,老年医学与药理,博士 2010.9-2012.7 北京理工大学,生命学院,神经生物学,硕士 2006.9-2010.7 青岛大学,医学院, 生物技术,学士 工作经历 2019.11-至今,北京理工大学,生命学院, 特别研究员 2016.3-2019.10 九州大学,齿学研究院,老年医学与药理,助理教授 主持及参与项目 国家自然科学基金委员会,面上项目,32070954,小胶质细胞及神经元的组织蛋白酶B参与阿尔兹海默病的发病机制研究,2021-1至2024-12, 58万元,在研,主持 北京市科学技术委员会,面上项目,7212066,组织蛋白酶B调节神经元功能在阿尔兹海默症中的作用及机制,2021-1至2023-12, 20万元,在研,主持 北京理工大学,科技创新计划,2020CX04166,组织蛋白酶E调节小胶质细胞功能在阿尔兹海默症中的作用及机制,2020-1至2022-12, 60万元,在研,主持 日本学术振兴会,青年学者科研基金,JP17K17093,The role of cathepsins in Aβ degradation in Alzheimer’s-like disease, 2017-4至2019-3, 416万日元(27.4万元),已结题,主持 日本学术振兴会,挑战萌芽基金,JP18K19650,The effects of gingipain on the pathogenesis of Alzheimer’s disease,2018-6至2021-3,637万日元(39万元),已结题,参与 国家自然科学基金委员会,面上项目,81171206, 早衰因子对β-分泌酶(BACE1)的调控与阿尔兹海默症致病机理的研究, 2012-01至2015-12,60万元,已结题,参与

研究领域

衰老及神经退行性疾病的分子机制 组织蛋白酶家族的病理学功能研究 小胶质细胞在生理及病理条件下的免疫特性研究 口腔疾病与脑认知功能的关系及机制研究

近期论文

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Ni, J.* & Wu, Z.* (2021) Inflammation Spreading: Negative Spiral Linking Systemic Inflammatory Disorders and Alzheimer's Disease, Front Cell Neurosci. 15, 638686. Zeng, F., Liu, Y., Huang, W., Qing, H., Kadowaki, T., Kashiwazaki, H., Ni, J.*& Wu, Z.* (2020) Receptor for advanced glycation end products up-regulation in cerebral endothelial cells mediates cerebrovascular-related amyloid beta accumulation after Porphyromonas gingivalis infection, J Neurochem. Meng, J., Liu, Y., Xie, Z., Qing, H.,*Lei, P.,*&Ni, J.* (2020) Nucleus distribution of cathepsin B in senescent microglia promotes brain aging through degradation of sirtuins, Neurobiol Aging. 96, 255-266. Jiang, M., Meng, J., Zeng, F., Qing, H., Hook, G., Hook, V., Wu, Z. * & Ni, J.* (2020) Cathepsin B inhibition blocks neurite outgrowth in cultured neurons by regulating lysosomal trafficking and remodeling, J Neurochem. 155, 300-312. Gu, Y., Wu, Z.*, Zeng, F., Jiang, M., Teeling, J. L., Ni, J.* & Takahashi, I.* (2020) Systemic Exposure to Lipopolysaccharide from Porphyromonas gingivalis Induces Bone Loss-Correlated Alzheimer's Disease-Like Pathologies in Middle-Aged Mice, J Alzheimers Dis. 78, 61-74. Nie, R., Wu, Z*., Ni, J., * Zeng, F., Yu, W., Zhang, Y., Kadowaki, T., Kashiwazaki, H., Teeling, J. L. & Zhou, Y*. (2019) Porphyromonas gingivalis Infection Induces Amyloid-beta Accumulation in Monocytes/Macrophages, J Alzheimers Dis. 72, 479-494. Ni, J., Wu, Z., Stoka, V., Meng, J., Hayashi, Y., Peters, C., Qing, H., Turk, V. & Nakanishi, H. (2019) Increased expression and altered subcellular distribution of cathepsin B in microglia induce cognitive impairment through oxidative stress and inflammatory response in mice, Aging Cell. 18, e12856. Ni, J., Wu, Z., Meng, J., Saito, T., Saido, T. C., Qing, H. & Nakanishi, H. (2019) An impaired intrinsic microglial clock system induces neuroinflammatory alterations in the early stage of amyloid precursor protein knock-in mouse brain, J Neuroinflammation. 16, 173. Wu, Z#., Ni, J#., Liu, Y., Teeling, J. L., Takayama, F., Collcutt, A., Ibbett, P. & Nakanishi, H. (2017) Cathepsin B plays a critical role in inducing Alzheimer's disease-like phenotypes following chronic systemic exposure to lipopolysaccharide from Porphyromonas gingivalis in mice, Brain Behav Immun. 65, 350-361. Ni, J#., Wu, Z#., Meng, J., Zhu, A., Zhong, X., Wu, S. & Nakanishi, H. (2017) The Neuroprotective Effects of Brazilian Green Propolis on Neurodegenerative Damage in Human Neuronal SH-SY5Y Cells, Oxid Med Cell Longev. 2017, 7984327. Dekita, M#., Wu, Z#., Ni, J#., Zhang, X., Liu, Y., Yan, X., Nakanishi, H. & Takahashi, I. (2017) Cathepsin S Is Involved in Th17 Differentiation Through the Upregulation of IL-6 by Activating PAR-2 after Systemic Exposure to Lipopolysaccharide from Porphyromonas gingivalis, Front Pharmacol. 8, 470. Ni, J., Wu, Z., Peterts, C., Yamamoto, K., Qing, H. & Nakanishi, H. (2015) The Critical Role of Proteolytic Relay through Cathepsins B and E in the Phenotypic Change of Microglia/Macrophage, J Neurosci. 35, 12488-501.

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