| First Author | Lee SH | Year | 2023 |
| Journal | Int J Mol Sci | Volume | 24 |
| Issue | 23 | PubMed ID | 38069392 |
| Mgi Jnum | J:348460 | Mgi Id | MGI:7566433 |
| Doi | 10.3390/ijms242317058 | Citation | Lee SH, et al. (2023) Second Wave, Late-Stage Neuroinflammation in Cleared Brains of Aged 5xFAD Alzheimer's Mice Detected by Macrolaser Light Sheet Microscopy Imaging. Int J Mol Sci 24(23) |
| abstractText | This study leverages the innovative imaging capabilities of macrolaser light-sheet microscopy to elucidate the 3D spatial visualization of AD-associated neuropathologic networks in the transparent brains of 44-week-old 5xFAD mice. Brain samples from ten AD and seven control mice were prepared through a hydrophilic tissue-clearing pipeline and immunostained with thioflavin S (beta-amyloid), anti-CD11b antibody (microglia), and anti-ACSA-2 antibody (astrocytes). The 5xFAD group exhibited significantly higher average total surface volumes of beta-amyloid accumulation than the control group (AD, 898,634,368 microm(3) [383,355,488-1,324,986,752]; control, 33,320,178 microm(3) [11,156,785-65,390,988], p = 0.0006). Within the AD group, there was significant interindividual and interindividual variability concerning the number and surface volume of individual amyloid particles throughout the entire brain. In the context of neuroinflammation, the 5xFAD group showed significantly higher average total surface volumes of anti-ACSA-2-labeled astrocytes (AD, 59,064,360 microm(3) [27,815,500-222,619,280]; control, 20,272,722 microm(3) [9,317,288-27,223,352], p = 0.0047) and anti-CD11b labeled microglia (AD, 51,210,100 microm(3) [15,309,118-135,532,144]; control, 23,461,593 microm(3) [14,499,170-27,924,110], p = 0.0162) than the control group. Contrary to the long-standing finding that early-stage neuroinflammation precedes the subsequent later-stage of neurodegeneration, our data reveal that the second wave, late-stage active neuroinflammation persists in the aged AD brains, even as they continue to show signs of ongoing neurodegeneration and significant amyloid accumulation. |
