Protection against hypoxia-induced increase in blood-brain barrier permeability: role of tight junction proteins and NFκB

RC Brown, KS Mark, RD Egleton… - Journal of Cell …, 2003 - journals.biologists.com
RC Brown, KS Mark, RD Egleton, JD Huber, AR Burroughs, TP Davis
Journal of Cell Science, 2003journals.biologists.com
Co-culture with glial cells and glia-conditioned media can induce blood-brain barrier
properties in microvessel endothelial cells and protect against hypoxia-induced blood-brain
barrier breakdown. We examined the effect of two types of glia-conditioned media on brain
microvessel endothelial cell permeability and tight junction protein expression, and studied
potential mechanisms of action. We found that C6-glioma-conditioned media, but not rat
astrocyte-conditioned media, protected against an increase in permeability induced by …
Co-culture with glial cells and glia-conditioned media can induce blood-brain barrier properties in microvessel endothelial cells and protect against hypoxia-induced blood-brain barrier breakdown. We examined the effect of two types of glia-conditioned media on brain microvessel endothelial cell permeability and tight junction protein expression, and studied potential mechanisms of action. We found that C6-glioma-conditioned media, but not rat astrocyte-conditioned media, protected against an increase in permeability induced by exposure to 1% oxygen for 24 hours. This hypoxic stress caused an increase in the expression of tight junction proteins claudin-1 and actin,particularly in cells treated with C6-conditioned media. We found that C6-conditioned media has a significantly higher level of both basic fibroblast growth factor and vascular endothelial growth factor. Treatment with C6-conditioned media for 1 or 3 days protects against hypoxia-induced permeability increases, and this protective effect may be mediated by signal transduction pathways terminating at the transcription factor NFκB.
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