Astrocyte–endothelial interactions and blood–brain barrier permeability

NJ Abbott - Journal of anatomy, 2002 - Wiley Online Library
NJ Abbott
Journal of anatomy, 2002Wiley Online Library
The blood–brain barrier (BBB) is formed by brain endothelial cells lining the cerebral
microvasculature, and is an important mechanism for protecting the brain from fluctuations in
plasma composition, and from circulating agents such as neurotransmitters and xenobiotics
capable of disturbing neural function. The barrier also plays an important role in the
homeostatic regulation of the brain microenvironment necessary for the stable and
coordinated activity of neurons. The BBB phenotype develops under the influence of …
The blood–brain barrier (BBB) is formed by brain endothelial cells lining the cerebral microvasculature, and is an important mechanism for protecting the brain from fluctuations in plasma composition, and from circulating agents such as neurotransmitters and xenobiotics capable of disturbing neural function. The barrier also plays an important role in the homeostatic regulation of the brain microenvironment necessary for the stable and coordinated activity of neurons. The BBB phenotype develops under the influence of associated brain cells, especially astrocytic glia, and consists of more complex tight junctions than in other capillary endothelia, and a number of specific transport and enzyme systems which regulate molecular traffic across the endothelial cells (Abbott & Romero, Mol. Medical Today2, 1996). Transporters characteristic of the BBB phenotype include both uptake mechanisms (e.g. GLUT‐1 glucose carrier, L1 amino acid transporter) and efflux transporters (e.g. P‐glycoprotein, MRP). In addition to their role in long‐term barrier induction and maintenance, astrocytes and other cells can release chemical factors that modulate endothelial permeability over a timescale of seconds to minutes.
Cell culture models, both primary and cell lines, have been used to investigate aspects of barrier induction and modulation. Conditioned medium taken from growing glial cells can reproduce some of the inductive effects, evidence for involvement of diffusible factors. However for some features of endothelial differentiation and induction the extracellular matrix plays an important role. Several candidate molecules have been identified capable of mimicking aspects of glial–mediated barrier induction of brain endothelium; these include TGF(GDNF, bFGF, IL‐6 and steroids. In addition factors secreted by brain endothelial cells including leukaemia inhibitory factor (LIF) have been shown to induce astrocytic differentiation. Thus endothelium and astrocytes are involved in 2‐way mutual induction. Short‐term modulation of brain endothelial permeability has been shown for a number of small chemical mediators produced by astrocytes and other nearby cell types. Thus endothelial cells are involved in both long and short‐term chemical communication with neighbouring cells, with the perivascular end feet of astrocytes being of particular importance. The role of barrier induction and modulation in normal physiology and in pathology will be discussed.
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