Regulation of Small GTPase Prenylation in the Nervous System

被引:19
|
作者
Reddy, Jairus M. [1 ]
Raut, Namrata G. R. [2 ]
Seifert, Jennifer L. [3 ]
Hynds, DiAnna L. [2 ,4 ]
机构
[1] Amer Inst Toxicol, Denton, TX USA
[2] Texas Womans Univ, Denton, TX 76204 USA
[3] TissueGen, North Richardson, TX USA
[4] Texas Womans Univ, Woodcock Inst Adv Neurocognit Res & Appl Practice, POB 4525799, Denton, TX 76204 USA
基金
美国国家科学基金会;
关键词
Farnesylation; Geranylgeranylation; Mevalonate pathway inhibitors; Prenyl transferases; Ras superfamily; Rho; Ras; Rab subfamilies; GERANYLGERANYL TRANSFERASE-I; BRAIN ISOPRENOIDS FARNESYL; PROTEIN PRENYLATION; ALZHEIMERS-DISEASE; PERILLYL ALCOHOL; SYNAPTIC-TRANSMISSION; MEVALONATE CASCADE; BETA-SECRETASE; INHIBITION; STATINS;
D O I
10.1007/s12035-020-01870-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Mevalonate pathway inhibitors have been extensively studied for their roles in cholesterol depletion and for inhibiting the prenylation and activation of various proteins. Inhibition of protein prenylation has potential therapeutic uses against neurological disorders, like neural cancers, neurodegeneration, and neurotramatic lesions. Protection against neurodegeneration and promotion of neuronal regeneration is regulated in large part by Ras superfamily small guanosine triphosphatases (GTPases), particularly the Ras, Rho, and Rab subfamilies. These proteins are prenylated to target them to cellular membranes. Prenylation can be specifically inhibited through altering the function of enzymes of the mevalonate pathway necessary for isoprenoid production and attachment to target proteins to elicit a variety of effects on neural cells. However, this approach does not address how prenylation affects a specific protein. This review focuses on the regulation of small GTPase prenylation, the different techniques to inhibit prenylation, and how this inhibition has affected neural cell processes.
引用
收藏
页码:2220 / 2231
页数:12
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