A beta 1-42-RAGE Interaction Disrupts Tight Junctions of the Blood-Brain Barrier Via Ca2+-Calcineurin Signaling
The blood-brain barrier (BBB), which is formed by adherens and tight junctions (TJs) of endothelial cells, maintains homeostasis of the brain. Disrupted intracellular Ca2+ homeostasis and breakdown of the BBB have been implicated in the pathogenesis of Alzheimer's disease (AD). The receptor for...
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Published in | The Journal of neuroscience Vol. 32; no. 26; pp. 8845 - 8854 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
27.06.2012
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Online Access | Get full text |
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Summary: | The blood-brain barrier (BBB), which is formed by adherens and tight junctions (TJs) of endothelial cells, maintains homeostasis of the brain. Disrupted intracellular Ca2+ homeostasis and breakdown of the BBB have been implicated in the pathogenesis of Alzheimer's disease (AD). The receptor for advanced glycation end products (RAGE) is known to interact with amyloid beta -peptide (A beta ) and mediate A beta transport across the BBB, contributing to the deposition of A beta in the brain. However, molecular mechanisms underlying A beta -RAGE interaction-induced alterations in the BBB have not been identified. We found that A beta 1-42 induces enhanced permeability, disruption of zonula occludin-1 (ZO-1) expression in the plasma membrane, and increased intracellular calcium and matrix metalloproteinase (MMP) secretion in cultured endothelial cells. Neutralizing antibodies against RAGE and inhibitors of calcineurin and MMPs prevented A beta 1-42-induced changes in ZO-1, suggesting that A beta -RAGE interactions alter TJ proteins through the Ca2+-calcineurin pathway. Consistent with these in vitro findings, we found disrupted microvessels near A beta plaque-deposited areas, elevated RAGE expression, and enhanced MMP secretion in microvessels of the brains of 5XFAD mice, an animal model for AD. We have identified a potential molecular pathway underlying A beta -RAGE interaction-induced breakage of BBB integrity. This pathway might play an important role in the pathogenesis of AD. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Feature-2 |
ISSN: | 1529-2401 |
DOI: | 10.1523/JNEUROSCI.6102-11.2012 |