Critical role of actin in modulating BBB permeability

被引:105
作者
Lai, CH
Kuo, KH
Leo, JM
机构
[1] Adv Peptide Med & Drug Delivery Res Lab, Chester Springs, PA 19425 USA
[2] Univ No British Columbia, No Med Program, Prince George, BC V2N 4Z9, Canada
[3] Univ British Columbia, Dept Anesthesiol Pharmacol & Therapeut, Vancouver, BC V6T 1Z3, Canada
[4] Univ British Columbia, St Pauls Hosp, James Hogg CAPTURE Ctr Cardiovasc & Pulm Res, Vancouver, BC V5Z 1M9, Canada
关键词
blood-brain barrier; tight junction; actin; cytoskeleton; cytochalasin;
D O I
10.1016/j.brainresrev.2005.03.007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A major obstacle in the treatment of degenerative manifestations and debilitating diseases in the central nervous system (CNS) ties in the impediment of drug delivery into these tissues. The impediment is due to a membrane barrier referred to as the blood-brain barrier (BBB). It is known that the BBB is a unique membranous structure in brain capillaries that tightly segregates the brain from systemic blood circulation. It is imperative to have a thorough understanding of the molecular components and their integrated function of this barrier to develop effective therapeutics for CNS disorders and diseases. Although there are other cell and biochemical properties that underlie this barrier function, it is well established that the barrier is mainly made up of the physical elements of tight junction (TJ) complex. The major constituents of TJ, such as occludin, claudins, zonula occludens (ZOs) and junctional adhesion molecule (JAM) have been subjects of intensive studies and reviews. However, after examining currently proposed models, we have come to believe that a cytoskeletal component-actin may play a. critical role in interacting TJ molecular constituents and modulating functional TJ complex. In this review, we will discuss the correlation of temporal and spatial distribution and remodeling of actin filaments with altering integrity of TJ complexes in various systems and present a hypothesis to depict its potential role in modulating BBB permeability. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:7 / 13
页数:7
相关论文
共 74 条
[1]   TIGHT JUNCTIONS AND THE MOLECULAR-BASIS FOR REGULATION OF PARACELLULAR PERMEABILITY [J].
ANDERSON, JM ;
VANITALLIE, CM .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1995, 269 (04) :G467-G475
[2]  
Aurrand-Lions MA, 2000, CURR TOP MICROBIOL, V251, P91
[3]   Transmembrane proteins of tight junctions [J].
Balda, MS ;
Matter, K .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2000, 11 (04) :281-289
[4]   Functional dissociation of paracellular permeability and transepithelial electrical resistance and disruption of the apical-basolateral intramembrane diffusion barrier by expression of a mutant tight junction membrane protein [J].
Balda, MS ;
Whitney, JA ;
Flores, C ;
Gonzalez, S ;
Cereijido, M ;
Matter, K .
JOURNAL OF CELL BIOLOGY, 1996, 134 (04) :1031-1049
[5]   The blood-brain barrier: an overview - Structure, regulation, and clinical implications [J].
Ballabh, P ;
Braun, A ;
Nedergaard, M .
NEUROBIOLOGY OF DISEASE, 2004, 16 (01) :1-13
[6]   Interaction of junctional adhesion molecule with the tight junction components ZO-1, cingulin, and occludin [J].
Bazzoni, G ;
Martínez-Estrada, OM ;
Orsenigo, F ;
Cordenonsi, M ;
Citi, S ;
Dejana, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (27) :20520-20526
[7]   EFFECT OF PLANT CYTOKININS ON MICROFILAMENTS AND TIGHT JUNCTION PERMEABILITY [J].
BENTZEL, CJ ;
HAINAU, B ;
EDELMAN, A ;
ANAGNOSTOPOULOS, T ;
BENEDETTI, EL .
NATURE, 1976, 264 (5587) :666-668
[8]   Involvement of RhoA and Rho kinase in neutrophil-stimulated endothelial hyperpermeability [J].
Breslin, JW ;
Yuan, SY .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2004, 286 (03) :H1057-H1062
[9]   Isolation and characterization of a novel oligodendrocyte-specific protein [J].
Bronstein, JM ;
Popper, P ;
Micevych, PE ;
Farber, DB .
NEUROLOGY, 1996, 47 (03) :772-778
[10]   Hypoxia/aglycemia alters expression of occludin and actin in brain endothelial cells [J].
Brown, RC ;
Davis, TP .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 327 (04) :1114-1123