Journal
BRAIN RESEARCH
Volume 1038, Issue 2, Pages 208-215Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.brainres.2005.01.027
Keywords
blood-brain barrier; pericyte; transforming growth factor-beta; P-glycoprotein; permeability; mouse brain endothelial cell
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The blood-brain barrier (BBB) is a highly organized multicellular complex consisting of an endothelium, brain pericytes and astrocytes. The present study was aimed at evaluating the role of brain pericytes in the induction and maintenance of BBB functions and involvement of transforming growth factor-beta (TGF-beta) in the functional properties of pericytes. We used an in vitro BBB model established by coculturing immortalized mouse brain capillary endothelial (MBEC4) cells with a primary culture of rat brain pericytes. The coculture with rat pericytes significantly decreased the permeability to sodium fluorescein and the accumulation of rhodamine 123 in MBEC4 cells, suggesting that brain pericytes induce and up-regulate the BBB functions. Rat brain pericytes expressed TGF-beta 1 mRNA. The pericyte-induced enhancement of BBB functions was significantly inhibited when cells were treated with anti-TGF-beta l antibody (10 mu g/ml) or a TGF-beta type I receptor antagonist (SB431542) (10 mu M) for 12 h. In MBEC4 monolayers, a 12 h exposure to TGF-beta 1 (1 ng/ml) significantly facilitated the BBB functions, this facilitation being blocked by SB431542. These findings suggest that brain pericytes contribute to the up-regulation of BBB functions through continuous TGF-beta production. (c) 2005 Elsevier B.V. All rights reserved.
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