Pharmacological Modulators of Tau Aggregation and Spreading

被引:23
|
作者
Dominguez-Meijide, Antonio [1 ,2 ]
Vasili, Eftychia [1 ]
Outeiro, Tiago Fleming [1 ,3 ,4 ]
机构
[1] Univ Med Ctr Goettingen, Ctr Biostruct Imaging Neurodegenerat, Dept Expt Neurodegenerat, D-37073 Gottingen, Germany
[2] Univ Santiago de Compostela, Dept Morphol Sci, Lab Neuroanat & Expt Neurol, IDIS,CIMUS, Santiago De Compostela 15782, Spain
[3] Max Planck Inst Expt Med, D-37075 Gottingen, Germany
[4] Newcastle Univ, Fac Med Sci, Translat & Clin Res Inst, Framlington Pl, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
关键词
tau; tauopathies; Alzheimer's disease; therapies; MICROTUBULE-ASSOCIATED PROTEIN; PAIRED HELICAL FILAMENTS; TRANSGENIC MOUSE MODEL; CSF BIOMARKERS PREDICT; ALZHEIMERS-DISEASE; METHYLENE-BLUE; ALPHA-SYNUCLEIN; ENDOGENOUS TAU; AMYLOID-BETA; CEREBROSPINAL-FLUID;
D O I
10.3390/brainsci10110858
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Tauopathies are neurodegenerative disorders characterized by the deposition of aggregates composed of abnormal tau protein in the brain. Additionally, misfolded forms of tau can propagate from cell to cell and throughout the brain. This process is thought to lead to the templated misfolding of the native forms of tau, and thereby, to the formation of newer toxic aggregates, thereby propagating the disease. Therefore, modulation of the processes that lead to tau aggregation and spreading is of utmost importance in the fight against tauopathies. In recent years, several molecules have been developed for the modulation of tau aggregation and spreading. In this review, we discuss the processes of tau aggregation and spreading and highlight selected chemicals developed for the modulation of these processes, their usefulness, and putative mechanisms of action. Ultimately, a stronger understanding of the molecular mechanisms involved, and the properties of the substances developed to modulate them, will lead to the development of safer and better strategies for the treatment of tauopathies.
引用
收藏
页码:1 / 29
页数:29
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