Cerebral amyloid-β proteostasis is regulated by the membrane transport protein ABCC1 in mice.

Abstract

In Alzheimer disease (AD), the intracerebral accumulation of amyloid-β (Aβ) peptides is a critical yet poorly understood process. Aβ clearance via the blood-brain barrier is reduced by approximately 30% in AD patients, but the underlying mechanisms remain elusive. ABC transporters have been implicated in the regulation of Aβ levels in the brain. Using a mouse model of AD in which the animals were further genetically modified to lack specific ABC transporters, here we have shown that the transporter ABCC1 has an important role in cerebral Aβ clearance and accumulation. Deficiency of ABCC1 substantially increased cerebral Aβ levels without altering the expression of most enzymes that would favor the production of Aβ from the Aβ precursor protein. In contrast, activation of ABCC1 using thiethylperazine (a drug approved by the FDA to relieve nausea and vomiting) markedly reduced Aβ load in a mouse model of AD expressing ABCC1 but not in such mice lacking ABCC1. Thus, by altering the temporal aggregation profile of Aβ, pharmacological activation of ABC transporters could impede the neurodegenerative cascade that culminates in the dementia of AD.

• Authors: Markus Krohn, Cathleen Lange, Jacqueline Hofrichter, Katja Scheffler, Jan Stenzel, Johannes Steffen, Toni Schumacher, Thomas Brüning, Anne-Sophie Plath, Franziska Alfen, Anke Schmidt, Felix Winter, Katja Rateitschak, Andreas Wree, Jörg Gsponer, Lary C Walker, Jens Pahnke
• Journal: The Journal of clinical investigation (J Clin Invest) Vol. 121 Issue 10 Pg. 3924-31 (Oct 2011) ISSN: 1558-8238 [Electronic] United States
• PMID: 21881209 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Chemical References

• Amyloid beta-Peptides
• Amyloid beta-Protein Precursor
• Multidrug Resistance-Associated Proteins
• multidrug resistance-associated protein 1

Topics

• Alzheimer Disease (etiology, genetics, metabolism)
• Amyloid beta-Peptides (chemistry, metabolism)
• Amyloid beta-Protein Precursor (chemistry, metabolism)
• Animals
• Brain (blood supply, metabolism, pathology)
• Disease Models, Animal
• Humans
• Mice
• Mice, Knockout
• Mice, Transgenic
• Microvessels (metabolism)
• Multidrug Resistance-Associated Proteins (deficiency, genetics, metabolism)
• Protein Multimerization