bioRxiv · 10.1101/2020.05.20.105064
Adenosine triphosphate Binding Cassette subfamily C member 1 (ABCC1) overexpression reduces APP processing and increases alpha- versus beta-secretase activity, in vitro
Abstract
The organic anion transporter Adenosine triphosphate Binding Cassette subfamily C member 1 (ABCC1), also known as MRP1, has been demonstrated in murine models of Alzheimers disease (AD) to export amyloid beta (Abeta) from the endothelial cells of the blood-brain barrier to the periphery, and that pharmaceutical activation of ABCC1 can reduce amyloid plaque deposition in the brain. Here, we show that ABCC1 is not only capable of exporting Abeta from the cytoplasm of human cells, but also that its overexpression significantly reduces Abeta production and increases the ratio of alpha- versus beta-secretase mediated cleavage of the Amyloid Precursor Protein (APP), likely via indirect modulation of alpha-, beta-, and gamma-secretase activity.
Source connections
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Jepsen, W. M., De Both, M., Siniard, A. L., Ramsey, K., Piras, I. S., Naymik, M., Henderson, A., Huentelman, M. J.. 2020-05-21. Adenosine triphosphate Binding Cassette subfamily C member 1 (ABCC1) overexpression reduces APP processing and increases alpha- versus beta-secretase activity, in vitro. https://doi.org/10.1101/2020.05.20.105064
Cite the original work for its findings. Save a collection to share your selection of sources.