| First Author | Choi J | Year | 2015 |
| Journal | Sci Transl Med | Volume | 7 |
| Issue | 314 | Pages | 314ra184 |
| PubMed ID | 26582899 | Mgi Jnum | J:234130 |
| Mgi Id | MGI:5789094 | Doi | 10.1126/scitranslmed.aad1904 |
| Citation | Choi J, et al. (2015) The E3 ubiquitin ligase Idol controls brain LDL receptor expression, ApoE clearance, and Abeta amyloidosis. Sci Transl Med 7(314):314ra184 |
| abstractText | Apolipoprotein E (ApoE) is an important modifier of Alzheimer's disease (AD) pathogenesis, and its abundance has been linked to the clearance of beta-amyloid (Abeta) in the brain. The pathways that control the clearance of ApoE in the brain are incompletely understood. We report that Idol, an E3 ubiquitin ligase that targets the low-density lipoprotein receptor (LDLR) for degradation, is a critical determinant of brain ApoE metabolism and Abeta plaque biogenesis. Previous work has shown that Idol contributes minimally to the regulation of hepatic LDLR expression in mice. By contrast, we demonstrate that Idol is a primary physiological regulator of LDLR protein in the brain, controlling the clearance of both ApoE-containing high-density lipoprotein (HDL) particles and Abeta. We studied the consequences of loss of Idol expression in a transgenic mouse model of Abeta amyloidosis. Idol deficiency increased brain LDLR, decreased ApoE, decreased soluble and insoluble Abeta, reduced amyloid plaque burden, and ameliorated neuroinflammation. These findings identify Idol as a gatekeeper of LDLR-dependent ApoE and Abeta clearance in the brain and a potential enzyme target for therapeutic intervention in AD. |
