The critical component to establish in vitro BBB model: Pericyte

被引:131
作者
Lai, CH
Kuo, KH
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 iCAPTURE Ctr Cardiovasc & Pulm Res, Vancouver, BC V6Z 1Y6, Canada
关键词
BBB; blood-brain barriers; pericyte; TGF-beta1; Rho GTPase; actin;
D O I
10.1016/j.brainresrev.2005.07.004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The blood-brain barrier (BBB), a highly regulated membranous barrier of brain capillaries, consists of an intricate network of tight junctions (TJs) that segregate the central nervous system (CNS) from systemic blood circulation and maintain a delicate homeostasis of the CNS environment. While endothelial cells (ECs) of brain capillaries are clearly the principal cellular element of BBB, the formation and regulation of intact BBB structure appear to require the interactions of endothelial cells with other cellular components. Astrocytes, one of the major non-neural cells in the brain, associate closely and interact with capillary endothelial cells during the angiogenesis and BBB development. Current in vitro Cellular models for the study of BBB functions often incorporate astrocytes with endothelial cells. However, another foremost cell type, CNS pericyte, which intimately embraces brain capillary endothelium, attracts relatively little attention for its role in developing the in vitro BBB system. This review will analyze the critical functions of pericytes in angiogenesis in various systems and discuss the relevance of these functions in mediating the development, maintenance, and regulation of BBB. The author will also discuss the functional role of actin in both ECs and pericytes, and further elaborate the molecular mechanisms of BBB permeability regulation that involves the transduction pathway-mediated actin remodeling process. Finally, the rationale of incorporating pericytes for establishing a better in vitro BBB model will be emphasized. (c) 2005 Elsevier B.V All rights reserved.
引用
收藏
页码:258 / 265
页数:8
相关论文
共 71 条
[1]   Astrocyte-endothelial interactions and blood-brain barrier permeability [J].
Abbott, NJ .
JOURNAL OF ANATOMY, 2002, 200 (06) :629-638
[2]  
Ahmad SA, 2001, CANCER RES, V61, P1255
[3]   Pericytes: Cell biology and pathology [J].
Allt, G ;
Lawrenson, JG .
CELLS TISSUES ORGANS, 2001, 169 (01) :1-11
[4]   AN ACTIVATED FORM OF TRANSFORMING GROWTH FACTOR-BETA IS PRODUCED BY COCULTURES OF ENDOTHELIAL-CELLS AND PERICYTES [J].
ANTONELLIORLIDGE, A ;
SAUNDERS, KB ;
SMITH, SR ;
DAMORE, PA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (12) :4544-4548
[5]   Contractile proteins in pericytes at the blood-brain and blood-retinal barriers [J].
Bandopadhyay, R ;
Orte, C ;
Lawrenson, JG ;
Reid, AR ;
De Silva, S ;
Allt, G .
JOURNAL OF NEUROCYTOLOGY, 2001, 30 (01) :35-44
[6]   Protein kinase A attenuates endothelial cell barrier dysfunction induced by microtubule disassembly [J].
Birukova, AA ;
Liu, F ;
Garcia, JGN ;
Verin, AD .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2004, 287 (01) :L86-L93
[7]  
BIRUKOVA AA, 2005, J CELL PHYSL
[8]   Transcription profiling of platelet-derived growth factor-B-deficient mouse embryos identifies RGS5 as a novel marker for pericytes and vascular smooth muscle cells [J].
Bondjers, C ;
Kalén, M ;
Hellström, M ;
Scheidl, SJ ;
Abramsson, A ;
Renner, O ;
Lindahl, P ;
Cho, HS ;
Kehrl, J ;
Betsholtz, C .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 162 (03) :721-729
[9]   RhoA and Rho-kinase dependent and independent signals mediate TGF-β-induced pulmonary endothelial cytoskeletal reorganization and permeability [J].
Clements, RT ;
Minnear, FL ;
Singer, HA ;
Keller, RS ;
Vincent, PA .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2005, 288 (02) :L294-L306
[10]   Superoxide mediated actin response in post-hypoxic endothelial cells [J].
Crawford, LE ;
Milliken, EE ;
Irani, K ;
Zweier, JL ;
Becker, LC ;
Johnson, TM ;
Eissa, NT ;
Crystal, RG ;
Finkel, T ;
GoldschmidtClermont, PJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (43) :26863-26867