神经胶质细胞炎症反应的RNA 调控及其作为中枢神经系统疾病治疗靶点的潜力

RNA Regulation of Inflammatory Responses in Glia and Its Potential as a Therapeutic Target in Central Nervous System Disorders

Abhishek Guha1,Mohammed Amir Husain1,Ying Si1,2,L Burt Nabors1,Natalia Filippova1,Grace Promer1,Reed Smith1,Peter H King1,2,3,4

1.Department Neurology,The University of Alabama at Birmingham,Birmingham,Alabama,USA.

2.Department Cell, Developmental, and Integrative Biology, The University of Alabama at Birmingham,Birmingham,Alabama,USA.

3.Birmingham Department of Veterans Health Care System,Birmingham,Alabama,USA.

4.Center for Neurodegeneration and Experimental Therapeutics, The University of Alabama at Birmingham,Birmingham,USA.

AbstractA major hallmark of neuroinflammation is the activation of microglia and astrocytes with the induction of inflammatory mediators such as IL-1β, TNF-α, iNOS, and IL-6.Neuroinflammation contributes to disease progression in a plethora of neurological disorders ranging from acute CNS trauma to chronic neurodegenerative disease.Posttranscriptional pathways of mRNA stability and translational efficiency are major drivers for the expression of these inflammatory mediators.A common element in this level of regulation centers around the adenine-and uridine-rich element(ARE)which is present in the 3’untranslated region(UTR)of the mRNAs encoding these inflammatory mediators.(ARE)-binding proteins(AUBPs)such as Human antigen R(HuR),Tristetraprolin (TTP) and KH- type splicing regulatory protein (KSRP) are key nodes for directing these posttranscriptional pathways and either promote(HuR)or suppress(TTP and KSRP)glial production of inflammatory mediators.This review will discuss basic concepts of ARE-mediated RNA regulation and its impact on glial-driven neuroinflammatory diseases.We will discuss strategies to target this novel level of gene regulation for therapeutic effect and review exciting preliminary studies that underscore its potential for treating neurological disorders.

KeywordsAU-rich element; HuR; chemokines; cytokines; glial cells; neuroinflammation; posttranscriptional regulation