Blood-brain barrier (BBB) endothelial cells lining the cerebral microvasculature maintain dynamic equilibrium between soluble amyloid-b (Ab) levels in the brain and plasma. The BBB dysfunction prevalent in Alzheimer disease contributes to the dysregulation of plasma and brain Ab and leads to the perturbation of the ratio between Ab42 and Ab40, the two most prevalent Ab isoforms in patients with Alzheimer disease. We hypothesize that BBB endothelium distinguishes between Ab40 and Ab42, distinctly modulates their trafficking kinetics between plasma and brain, and thereby contributes to the maintenance of healthy Ab42/Ab40 ratios. To test this hypothesis, we investigated Ab40 and Ab42 trafficking kinetics in hCMEC/D3 monolayers (human BBB cell culture model) in vitro as well as in mice in vivo. Although the rates of uptake of fluorescein-labeled Ab40 and Ab42 (F-Ab40 and F-Ab42) were not significantly different on the abluminal side, the luminal uptake rate of F-Ab42 was substantially higher than F-Ab40. Since higher plasma Ab levels were shown to aggravate BBB dysfunction and trigger cerebrovascular disease, we systematically investigated the dynamic interactions of luminal [125I]Ab peptides and their trafficking kinetics at BBB using single-photon emission computed tomography/computed tomography imaging in mice. Quantitative modeling of the dynamic imaging data thus obtained showed that the rate of uptake of toxic [125I]Ab42 and its subsequent BBB transcytosis is significantly higher than [125I]Ab40. It is likely that the molecular mechanisms underlying these kinetic differences are differentially affected in Alzheimer and cerebrovascular diseases, impact plasma and brain levels of Ab40 and Ab42, engender shifts in the Ab42/Ab40 ratio, and unleash downstream toxic effects. SIGNIFICANCE STATEMENT Dissecting the binding and uptake kinetics of Ab40 and Ab42 at the BBB endothelium will facilitate the estimation of Ab40 versus Ab42 exposure to the BBB endothelium and allow assessment of the risk of BBB dysfunction by monitoring Ab42 and Ab40 levels in plasma. This knowledge, in turn, will aid in elucidating the role of these predominant Ab isoforms in aggravating BBB dysfunction and cerebrovascular disease.
|Original language||English (US)|
|Number of pages||9|
|Journal||Journal of Pharmacology and Experimental Therapeutics|
|State||Published - 2021|
ASJC Scopus subject areas
- Molecular Medicine