Disruption of the tight junctions (TJs) of the blood-brain barrier (BBB) is
a hallmark of many CNS pathologies, including stroke, HIV encephalitis, Al
zheimer's disease, multiple sclerosis and bacterial meningitis. Furthermore
, systemic-derived inflammation has recently been shown to cause BBB tight
junctional disruption and increased paracellular permeability. The BBB is c
apable of rapid modulation in response to physiological stimuli at the cyto
skeletal level, which enables it to protect the brain parenchyma and mainta
in a homeostatic environment. By allowing the 'loosening' of Us and an incr
ease in paracellular permeability, the BBB is able to 'bend without breakin
g'; thereby, maintaining structural integrity.