Mesoscopic Mapping of Visual Pathway in a Female 5XFAD Mouse Model of Alzheimer's Diseaseopen accessMesoscopic Mapping of Visual Pathway in a Female 5XFAD Mouse Model of Alzheimer's Disease
- Other Titles
- Mesoscopic Mapping of Visual Pathway in a Female 5XFAD Mouse Model of Alzheimer's Disease
- Authors
- Nam Yunkwon; Kim Sujin; Kim Jieun; Hoe Hyang-Sook; Moon Minho
- Issue Date
- Dec-2022
- Publisher
- Multidisciplinary Digital Publishing Institute (MDPI)
- Keywords
- Alzheimer' s disease; visual pathway; 5XFAD mice; cholera toxin beta subunits
- Citation
- Cells, v.11, no.23
- Journal Title
- Cells
- Volume
- 11
- Number
- 23
- URI
- http://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/171
- DOI
- 10.3390/cells11233901
- ISSN
- 2073-4409
- Abstract
- Amyloid-beta (A beta) deposition and A beta-induced neurodegeneration appear in the retina and retinorecipient areas in the early stages of Alzheimer's disease (AD). Although these A beta-related changes in the retina cause damage to the visual functions, no studies have yet revealed the alterations in the visual pathways of AD. Therefore, we investigated the alterations of visual circuits in the AD mouse model using anterograde tracer cholera toxin beta subunits (CT beta). Moreover, we investigated the A beta accumulation in the retina and retinorecipient areas and the neuronal loss, and synaptic degeneration in retinorecipient areas by immunofluorescent staining of 4- and 12-month-old female 5XFAD transgenic mice. Our results demonstrated that A beta accumulation and neurodegeneration occurred in the retina and retinorecipient regions of early and late stages of the 5XFAD mice. Retinal efferents to the suprachiasmatic nucleus and lateral geniculate nucleus were impaired in the early stage of AD. Moreover, retinal connections to the dorsal lateral geniculate nucleus and superior colliculus were degenerated in the late-stage of AD. These findings reveal the A beta-related pathology induced visual circuit disturbances at the mesoscale level in both the early and late stages of AD and provide anatomical and functional insights into the visual circuitry of AD.
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