Effects of a Disrupted Blood-Brain Barrier on Cholesterol Homeostasis in the Brain

• Published in: The Journal of biological chemistry 2014-08, Vol.289 (34), p.23712-23722
• Main Authors: Saeed, Ahmed A., Genové, Guillem, Li, Tian, Lütjohann, Dieter, Olin, Maria, Mast, Natalia, Pikuleva, Irina A., Crick, Peter, Wang, Yuqin, Griffiths, William, Betsholtz, Christer, Björkhem, Ingemar
• Format: Article
• Language: English
• Subjects: Animals; Base Sequence; Blood-Brain Barrier; Brain - metabolism; Cholesterol - biosynthesis; Cholesterol - metabolism; DNA Primers; Genes, sis; Homeostasis - genetics; Lipids; Medicin och hälsovetenskap; Mice; Mice, Transgenic; Plants - metabolism; Real-Time Polymerase Chain Reaction; Sterols - metabolism
• ISSN: 0021-9258; 1083-351X; 1083-351X
• DOI: 10.1074/jbc.M114.556159

The presence of the blood-brain barrier (BBB) is critical for cholesterol metabolism in the brain, preventing uptake of lipoprotein-bound cholesterol from the circulation. The metabolic consequences of a leaking BBB for cholesterol metabolism have not been studied previously. Here we used a pericyte-deficient mouse model, Pdgfbret/ret, shown to have increased permeability of the BBB to a range of low-molecular mass and high-molecular mass tracers. There was a significant accumulation of plant sterols in the brains of the Pdgfbret/ret mice. By dietary treatment with 0.3% deuterium-labeled cholesterol, we could demonstrate a significant flux of cholesterol from the circulation into the brains of the mutant mice roughly corresponding to about half of the measured turnover of cholesterol in the brain. We expected the cholesterol flux into the brain to cause a down-regulation of cholesterol synthesis. Instead, cholesterol synthesis was increased by about 60%. The levels of 24(S)-hydroxycholesterol (24S-OHC) were significantly reduced in the brains of the pericyte-deficient mice but increased in the circulation. After treatment with 1% cholesterol in diet, the difference in cholesterol synthesis between mutants and controls disappeared. The findings are consistent with increased leakage of 24S-OHC from the brain into the circulation in the pericyte-deficient mice. This oxysterol is an efficient suppressor of cholesterol synthesis, and the results are consistent with a regulatory role of 24S-OHC in the brain. To our knowledge, this is the first demonstration that a defective BBB may lead to increased flux of a lipophilic compound out from the brain. The relevance of the findings for the human situation is discussed.