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Disruption of brain-blood barrier might influence progression of Alzheimer’s

More and more data from preclinical and clinical studies strengthen the hypothesis that immune system-mediated actions contribute to and drive pathogenesis in Alzheimer’s disease. The team of in the (VIB/UGent) combined their knowledge and expertise related to inflammation with the expertise in Alzheimer’s disease present in the (VIB/KU Leuven). This collaboration lead to the insights that A? indeed induces a strong inflammatory response, thereby destroying an important but often neglected brain barrier, called the blood- (CSF) barrier. Disruption of this blood-CSF barrier disturbs brain homeostasis and might negatively affect . Strikingly, these effects could be blocked in the presence of a matrix metalloproteinase (MMP) inhibitor.

Roosmarijn Vandenbroucke: “Although further research is needed, these data suggest that blocking MMP activity or upstream inflammatory signalling, might have therapeutic potential to treat Alzheimer’s disease. It is important we could demonstrate the role of the blood-cerebrospinal fluid barrier, because this would be an easier target to reach in comparison with the targets of current therapies.”

The publication of Vandenbroucke et al. was picked up by Alzforum.org who combined it together with another publication about the Blood-Brain Barrier: Barriers Between Blood and CSF, Brain Yield to A? – Not a Bad Thing? 18 Sep 2015.

The barrier between the blood and central nervous system crumbles in Alzheimer’s disease, but researchers have known little about how this happens, or what it does to brain pathology. Two new papers shed some light on how A? damages the cells that protect the brain parenchyma and cerebrospinal fluid. The studies examine different systems and describe distinct mechanisms, but both add to the picture of what may happen in disease.