Therapeutic Targeting of Rab GTPases: Relevance for Alzheimer's Disease

被引:12
|
作者
Jordan, Kate L. [1 ]
Koss, David J. [2 ]
Outeiro, Tiago F. [2 ,3 ,4 ,5 ]
Giorgini, Flaviano [1 ]
机构
[1] Univ Leicester, Dept Genet & Genome Biol, Univ Rd, Leicester LE1 7RH, Leics, England
[2] Newcastle Univ, Fac Med Sci, Translat & Clin Res Inst, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[3] Univ Med Ctr Gottingen, Ctr Biostruct Imaging Neurodegenerat, Dept Expt Neurodegenerat, D-37075 Gottingen, Germany
[4] Max Planck Inst Nat Sci, D-37075 Gottingen, Germany
[5] Deutsch Zentrum Neurodegenerat Erkrankungen DZNE, D-37075 Gottingen, Germany
基金
英国医学研究理事会;
关键词
Rab GTPases; Alzheimer's; neurodegeneration; AMYLOID PRECURSOR PROTEIN; GTP-BINDING PROTEIN; MILD COGNITIVE IMPAIRMENT; TRANS-GOLGI NETWORK; MEMBRANE TRAFFICKING; UP-REGULATION; GERANYLGERANYL TRANSFERASE; ENDOPLASMIC-RETICULUM; MUTANT HUNTINGTIN; SYNAPTIC PROTEINS;
D O I
10.3390/biomedicines10051141
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Rab GTPases (Rabs) are small proteins that play crucial roles in vesicle transport and membrane trafficking. Owing to their widespread functions in several steps of vesicle trafficking, Rabs have been implicated in the pathogenesis of several disorders, including cancer, diabetes, and multiple neurodegenerative diseases. As treatments for neurodegenerative conditions are currently rather limited, the identification and validation of novel therapeutic targets, such as Rabs, is of great importance. This review summarises proof-of-concept studies, demonstrating that modulation of Rab GTPases in the context of Alzheimer's disease (AD) can ameliorate disease-related phenotypes, and provides an overview of the current state of the art for the pharmacological targeting of Rabs. Finally, we also discuss the barriers and challenges of therapeutically targeting these small proteins in humans, especially in the context of AD.
引用
收藏
页数:25
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