Novel monoclonal antibodies targeting the microtubule-binding domain of human tau

被引:11
作者
Craft, Cara L. [1 ,2 ]
Moore, Brenda D. [1 ,2 ]
Ran, Yong [1 ,2 ]
Chakrabarty, Paramita [1 ,2 ,3 ]
Levites, Yona [1 ,2 ,3 ]
Golde, Todd E. [1 ,2 ,3 ]
Giasson, Benoit I. [1 ,2 ,3 ]
机构
[1] Univ Florida, Coll Med, Dept Neurosci, Gainesville, FL 32610 USA
[2] Univ Florida, Coll Med, Ctr Translat Res Neurodegenerat Dis, Gainesville, FL 32611 USA
[3] Univ Florida, Coll Med, McKnight Brain Inst, Gainesville, FL 32611 USA
关键词
PAIRED HELICAL FILAMENTS; PROGRESSIVE SUPRANUCLEAR PALSY; ALZHEIMERS-DISEASE; NEUROFIBRILLARY TANGLES; CORTICOBASAL DEGENERATION; PICKS-DISEASE; MOUSE MODEL; PROTEIN-TAU; HUMAN-BRAIN; ISOFORMS;
D O I
10.1371/journal.pone.0195211
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Tauopathies including Alzheimer's disease and Progressive Supranuclear Palsy are a diverse group of progressive neurodegenerative disorders pathologically defined by inclusions containing aberrantly aggregated, post-translationally modified tau. The tau pathology burden correlates with neurodegeneration and dementia observed in these diseases. The microtubule binding domain of tau is essential for its physiological functions in promoting neuronal cytoskeletal stability, however it is also required for tau to assemble into an amyloid structure that comprises pathological inclusions. A series of novel monoclonal antibodies were generated which recognize the second and fourth microtubule-binding repeat domain of tau, thus enabling the identification specifically of 4-repeat tau versus 3-/4-repeat tau, respectively. These antibodies are highly specific for tau and recognize pathological tau inclusions in human tauopathies including Alzheimer's disease and Progressive Supranuclear Palsy and in transgenic mouse models of tauopathies. These new antibodies will be useful for identifying and characterizing different tauopathies and as tools to target tau pathology in these diseases.
引用
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页数:13
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