Amyloid-beta transporter expression at the choroid plexus in normal aging: the possibility of reduced resistance to oxidative stress insults.
- Author:
Chong-Bin LIU
1
,
2
;
Rui WANG
;
Miao-Wu DONG
;
Xi-Ren GAO
;
Feng YU
Author Information
1. Departments of Physiology and Pharmacology, School of Medicine, Huzhou Teachers College, Huzhou 313000, China
2. Department of Physiology, Wenzhou Medical University, Wenzhou 325000, China. liuchongbin1972@126.com.
- Publication Type:Journal Article
- MeSH:
ATP Binding Cassette Transporter, Sub-Family B;
metabolism;
Aging;
Amyloid beta-Peptides;
metabolism;
Animals;
Caspase 3;
metabolism;
Choroid Plexus;
physiology;
Heme Oxygenase (Decyclizing);
metabolism;
LDL-Receptor Related Proteins;
metabolism;
Oxidative Stress;
Peptide Fragments;
metabolism;
Rats;
Receptor for Advanced Glycation End Products;
Receptors, Immunologic;
metabolism
- From:
Acta Physiologica Sinica
2014;66(2):158-168
- CountryChina
- Language:English
-
Abstract:
Accumulation of amyloid-beta peptides (Aβ) results in amyloid burden in normal aging brain. Clearance of this peptide from the brain occurs via active transport at the interfaces separating the central nervous system (CNS) from the peripheral circulation. The present study was to investigate the change of Aβ transporters expression at the choroid plexus (CP) in normal aging. Morphological modifications of CP were observed by transmission electron microscope. Real-time RT-PCR was used to measure mRNA expressions of Aβ(42) and its transporters, which include low density lipoprotein receptor-related protein-1 and 2 (LRP-1 and -2), P-glycoprotein (P-gp) and the receptor for advanced glycation end-products (RAGE), at the CP epithelium in rats at ages of 3, 6, 9, 12, 15, 18, 21, 24, 27, 30, 33 and 36 months. At the same time, the mRNA expressions of oxidative stress-related proteins were also measured. The results showed that a striking deterioration of the CP epithelial cells and increased Aβ(42) mRNA expression were observed in aged rats, and there was a decrease in the transcription of the Aβ efflux transporters, LRP-1 and P-gp, no change in RAGE mRNA expression and an increase in LRP-2, the CP epithelium Aβ influx transporter. Heme oxygenase-1 (HO-1) and caspase-3 expressions at the CP epithelium increased with age at the mRNA level. These results suggest the efficacy of the CP in clearing of Aβ deceases in normal aging, which results in the increase of brain Aβ accumulation. And excess Aβ interferes with oxidative phosphorylation, leads to oxidative stress and morphological structural changes. This in turn induces further pathological cascades of toxicity, inflammation and neurodegeneration process.
