Regulation of ABC efflux transporters at blood-brain barrier in health and neurological disorders

被引:171
|
作者
Qosa, Hisham [1 ]
Miller, David S. [2 ]
Pasinelli, Piera [1 ]
Trotti, Davide [1 ]
机构
[1] Thomas Jefferson Univ, Dept Neurosci, Farber Inst Neurosci, Weinberg Unit ALS Res, Philadelphia, PA 19107 USA
[2] NIEHS, Lab Signal Transduct, NIH, Res Triangle Pk, NC 27709 USA
关键词
ABC efflux transporters; Blood-brain barrier; Neuroprotection; Pharmacoresistance; P-GLYCOPROTEIN EXPRESSION; CANCER RESISTANCE PROTEIN; BINDING CASSETTE TRANSPORTERS; MEDIATED UP-REGULATION; TUMOR-NECROSIS-FACTOR; DIESEL EXHAUST PARTICLES; CULTURED RAT ASTROCYTES; AMYLOID-BETA CLEARANCE; NF-KAPPA-B; MULTIDRUG-RESISTANCE;
D O I
10.1016/j.brainres.2015.07.005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The strength of the blood-brain barrier (BBB) in providing protection to the central nervous system from exposure to circulating chemicals is maintained by tight junctions between endothelial cells and by a broad range of transporter proteins that regulate exchange between CNS and blood. The most important transporters that restrict the permeability of large number of toxins as well as therapeutic agents are the ABC transporters. Among them, P-gp, BCRP, MRP1 and MRP2 are the utmost studied. These efflux transporters are neuroprotective, limiting the brain entry of neurotoxins; however, they could also restrict the entry of many therapeutics and contribute to CNS pharmacoresistance. Characterization of several regulatory pathways that govem expression and activity of ABC efflux transporters in the endothelium of brain capillaries have led to an emerging consensus that these processes are complex and contain several cellular and molecular elements. Alterations in ABC efflux transporters expression and/or activity occur in several neurological diseases. Here, we review the signaling pathways that regulate expression and transport activity of P-gp, BCRP, MRP1 and MRP2 as well as how their expression/activity changes in neurological diseases. This article is part of a Special Issue entitled SI: Neuroprotection. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:298 / 316
页数:19
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