Amyloid pathology and cognitive impairment in hAβ-KI and APPSAA-KI mouse models of Alzheimer's disease

The hAβ-KI and APP<sup>SAA</sup>-KI are two amyloid models that harbor mutations in the endogenous mouse App gene. Both hAβ-KI and APP<sup>SAA</sup>-KI mice contain a humanized Aβ sequence, and APP<sup>SAA</sup>-KI mice carry three additional familial AD mutations. We herein report that the Aβ levels and Aβ42/Aβ40 ratio in APP<sup>SAA</sup>-KI homozygotes are dramatically higher than those in hAβ-KI homozygotes at 14 months of age. In addition, APP<sup>SAA</sup>-KI mice display a widespread distribution of amyloid plaques in the brain, whereas the plaques are undetectable in hAβ-KI mice. Moreover, there are no sex differences in amyloid pathology in APP<sup>SAA</sup>-KI mice. Both APP<sup>SAA</sup>-KI and hAβ-KI mice exhibit cognitive impairments, wherein no significant differences are found between these two models, although APP<sup>SAA</sup> KI mice show a trend towards worse cognitive function. Notably, female hAβ-KI and APP<sup>SAA</sup>-KI mice have a more pronounced cognitive impairments compared to their respective males. Our findings suggest that Aβ humanization contributes to cognitive deficits in APP<sup>SAA</sup>-KI mice, and that amyloid deposition might not be closely associated with cognitive impairments in APP<sup>SAA</sup>-KI mice.

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Publication Details

Journal
Neurobiology of Aging
Published
2024-10-19
DOI
https://doi.org/10.1016/j.neurobiolaging.2024.10.005
Citations
6
Primary Topic
Alzheimer's disease research and treatments
Type
article
Field-Weighted Citation Impact
1.96

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article

Amyloid pathology and cognitive impairment in hAβ-KI and APPSAA-KI mouse models of Alzheimer's disease

Wenyan Lü, Guojun Bu, Francis Shue, Jesse R. Macyczko et al.
6 citations
Neurobiology of Aging
Alzheimer's disease research and treatments
1.96
article

Amyloid pathology and cognitive impairment in hAβ-KI and APPSAA-KI mouse models of Alzheimer's disease

Wenyan Lü, Guojun Bu, Francis Shue, Jesse R. Macyczko, Takahisa Kanekiyo, Suren Jeevaratnam, Bhaskar Roy, Ni Wang, Yonghe Li, Aishe Kurti, Taha Izhar
article en
6 citations

Abstract

The hAβ-KI and APP<sup>SAA</sup>-KI are two amyloid models that harbor mutations in the endogenous mouse App gene. Both hAβ-KI and APP<sup>SAA</sup>-KI mice contain a humanized Aβ sequence, and APP<sup>SAA</sup>-KI mice carry three additional familial AD mutations. We herein report that the Aβ levels and Aβ42/Aβ40 ratio in APP<sup>SAA</sup>-KI homozygotes are dramatically higher than those in hAβ-KI homozygotes at 14 months of age. In addition, APP<sup>SAA</sup>-KI mice display a widespread distribution of amyloid plaques in the brain, whereas the plaques are undetectable in hAβ-KI mice. Moreover, there are no sex differences in amyloid pathology in APP<sup>SAA</sup>-KI mice. Both APP<sup>SAA</sup>-KI and hAβ-KI mice exhibit cognitive impairments, wherein no significant differences are found between these two models, although APP<sup>SAA</sup> KI mice show a trend towards worse cognitive function. Notably, female hAβ-KI and APP<sup>SAA</sup>-KI mice have a more pronounced cognitive impairments compared to their respective males. Our findings suggest that Aβ humanization contributes to cognitive deficits in APP<sup>SAA</sup>-KI mice, and that amyloid deposition might not be closely associated with cognitive impairments in APP<sup>SAA</sup>-KI mice.

Neurobiology of AgingVol. 145
Jacksonville College (US), Mayo Clinic in Florida (US)
National Institutes of Health
Openalex Percentile: Top 13%
Alzheimer's disease research and treatments
1.96
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