| First Author | Huynh TN | Year | 2024 |
| Journal | Int J Mol Sci | Volume | 25 |
| Issue | 24 | PubMed ID | 39769453 |
| Mgi Jnum | J:361222 | Mgi Id | MGI:7854275 |
| Doi | 10.3390/ijms252413690 | Citation | Huynh TN, et al. (2024) Inhibiting the Cholesterol Storage Enzyme ACAT1/SOAT1 in Aging Apolipoprotein E4 Mice Alters Their Brains' Inflammatory Profiles. Int J Mol Sci 25(24) |
| abstractText | Aging and apolipoprotein E4 (APOE4) are the two most significant risk factors for late-onset Alzheimer's disease (LOAD). Compared to APOE3, APOE4 disrupts cholesterol homeostasis, increases cholesteryl esters (CEs), and exacerbates neuroinflammation in brain cells, including microglia. Targeting CEs and neuroinflammation could be a novel strategy to ameliorate APOE4-dependent phenotypes. Toll-like receptor 4 (TLR4) is a key macromolecule in inflammation, and its regulation is associated with the cholesterol content of lipid rafts in cell membranes. We previously demonstrated that in normal microglia expressing APOE3, inhibiting the cholesterol storage enzyme acyl-CoA:cholesterol acyltransferase 1 (ACAT1/SOAT1) reduces CEs, dampened neuroinflammation via modulating the fate of TLR4. We also showed that treating myelin debris-loaded normal microglia with ACAT inhibitor F12511 reduced cellular CEs and activated ABC transporter 1 (ABCA1) for cholesterol efflux. This study found that treating primary microglia expressing APOE4 with F12511 also reduces CEs, activates ABCA1, and dampens LPS-dependent NFkappaB activation. In vivo, two-week injections of nanoparticle F12511, which consists of DSPE-PEG(2000), phosphatidylcholine, and F12511, to aged female APOE4 mice reduced TLR4 protein content and decreased proinflammatory cytokines, including IL-1beta in mice brains. Overall, our work suggests nanoparticle F12511 is a novel agent to ameliorate LOAD. |
