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多肽靶向嵌合体通过促进tau蛋白特异性去磷酸化治疗阿尔茨海默病和其他tau蛋白病(英文)

Generation of tau dephosphorylation-targeting chimeras for the treatment of Alzheimer’s disease and related tauopathies

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【作者】 苏静芬肖越魏林郁雷慧杨孙飞王围霞尹君熊瑞李师宏张配周颖王小川郑杰王建枝

【Author】 Jingfen Su;Yue Xiao;Linyu Wei;Huiyang Lei;Fei Sun;Weixia Wang;Jun Yin;Rui Xiong;Shihong Li;Pei Zhang;Ying Zhou;Xiaochuan Wang;Jie Zheng;Jian-Zhi Wang;Department of Pathophysiology, School of Basic Medicine, Key Laboratory of Education Ministry of China/Hubei Province for Neurological Disorders, Tongji Medical College, Huazhong University of Science and Technology;School of Artificial Intelligence and Automation, Huazhong University of Science and Technology;Sino-UK Joint Laboratory of Brain Function and Injury of Henan Province, Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Xinxiang Medical University;Department of Pathophysiology, School of Basic Medical Sciences, Wuhan University;Department of Anesthesiology, The First Affiliated Hospital of Gannan Medical University;The Core Facility and Technical Support, Wuhan Institute of Virology, Chinese Academy of Sciences;Research Center for Medicine and Structural Biology, Wuhan University;Neuroscience Research Institute and Department of Neurobiology, School of Basic Medical Sciences, Peking University, Key Laboratory for Neuroscience, Ministry of Education/National Health Commission;Co-innovation Center of Neuroregeneration, Nantong University;

【通讯作者】 王小川;郑杰;王建枝;

【机构】 Department of Pathophysiology, School of Basic Medicine, Key Laboratory of Education Ministry of China/Hubei Province for Neurological Disorders, Tongji Medical College, Huazhong University of Science and TechnologySchool of Artificial Intelligence and Automation, Huazhong University of Science and TechnologySino-UK Joint Laboratory of Brain Function and Injury of Henan Province, Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Xinxiang Medical UniversityDepartment of Pathophysiology, School of Basic Medical Sciences, Wuhan UniversityDepartment of Anesthesiology, The First Affiliated Hospital of Gannan Medical UniversityThe Core Facility and Technical Support, Wuhan Institute of Virology, Chinese Academy of SciencesResearch Center for Medicine and Structural Biology, Wuhan UniversityNeuroscience Research Institute and Department of Neurobiology, School of Basic Medical Sciences, Peking University, Key Laboratory for Neuroscience, Ministry of Education/National Health CommissionCo-innovation Center of Neuroregeneration, Nantong University

【摘要】 Abnormal hyperphosphorylation and accumulation of tau protein play a pivotal role in neurodegeneration in Alzheimer’s disease(AD) and many other tauopathies.Selective elimination of hyperphosphorylated tau is promising for the therapy of these diseases.We have conceptualized a strategy,named dephosphorylation-targeting chimeras(DEPTACs),for specifically hijacking phosphatases to tau to debilitate its hyperphosphorylation.Here,we conducted the step-by-step optimization of each constituent motif to generate DEPTACs with reasonable effectiveness in facilitating the dephosphorylation and subsequent clearance of pathological tau.Specifically,for one of the selected chimeras,D16,we demonstrated its significant efficiency in rescuing the neurodegeneration caused by neurotoxic K18-tau seeds in vitro.Moreover,intravenous administration of D16 also alleviated tau pathologies in the brain and improved memory deficits in AD mice.These results suggested DEPTACs as targeted modulators of tau phosphorylation,which hold therapeutic potential for AD and other tauopathies.

【Abstract】 Abnormal hyperphosphorylation and accumulation of tau protein play a pivotal role in neurodegeneration in Alzheimer’s disease(AD) and many other tauopathies.Selective elimination of hyperphosphorylated tau is promising for the therapy of these diseases.We have conceptualized a strategy,named dephosphorylation-targeting chimeras(DEPTACs),for specifically hijacking phosphatases to tau to debilitate its hyperphosphorylation.Here,we conducted the step-by-step optimization of each constituent motif to generate DEPTACs with reasonable effectiveness in facilitating the dephosphorylation and subsequent clearance of pathological tau.Specifically,for one of the selected chimeras,D16,we demonstrated its significant efficiency in rescuing the neurodegeneration caused by neurotoxic K18-tau seeds in vitro.Moreover,intravenous administration of D16 also alleviated tau pathologies in the brain and improved memory deficits in AD mice.These results suggested DEPTACs as targeted modulators of tau phosphorylation,which hold therapeutic potential for AD and other tauopathies.

【基金】 supported by the National Natural Science Foundation of China (82230041,91949205,31730035,81721005);the National Key R&D Program of China (2016YFC1305800);the Guangdong Provincial Key S&T Program (018B030336001)
  • 【文献出处】 Science Bulletin ,科学通报(英文) , 编辑部邮箱 ,2024年08期
  • 【分类号】R749.16
  • 【下载频次】76
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