Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA.
Department of Neuroscience, Mayo Clinic, Jacksonville, FL 32224, USA.
Neurobiol Aging. 2025 Jan;145:13-23. doi: 10.1016/j.neurobiolaging.2024.10.005. Epub 2024 Oct 19.
The hAβ-KI and APP-KI are two amyloid models that harbor mutations in the endogenous mouse App gene. Both hAβ-KI and APP-KI mice contain a humanized Aβ sequence, and APP-KI mice carry three additional familial AD mutations. We herein report that the Aβ levels and Aβ42/Aβ40 ratio in APP-KI homozygotes are dramatically higher than those in hAβ-KI homozygotes at 14 months of age. In addition, APP-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-KI mice. Both APP-KI and hAβ-KI mice exhibit cognitive impairments, wherein no significant differences are found between these two models, although APP KI mice show a trend towards worse cognitive function. Notably, female hAβ-KI and APP-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-KI mice, and that amyloid deposition might not be closely associated with cognitive impairments in APP-KI mice.
hAβ-KI 和 APP-KI 是两种携带有内源性小鼠 App 基因突变的淀粉样蛋白模型。hAβ-KI 和 APP-KI 小鼠均含有人源化 Aβ 序列,APP-KI 小鼠还携带三种额外的家族性 AD 突变。我们在此报告,在 14 月龄时,APP-KI 纯合子小鼠的 Aβ 水平和 Aβ42/Aβ40 比值明显高于 hAβ-KI 纯合子小鼠。此外,APP-KI 小鼠的大脑中存在广泛分布的淀粉样斑块,而 hAβ-KI 小鼠则无法检测到这些斑块。此外,APP-KI 小鼠的淀粉样蛋白病理没有性别差异。APP-KI 和 hAβ-KI 小鼠均表现出认知障碍,尽管 APP KI 小鼠的认知功能有下降趋势,但这两种模型之间没有发现显著差异。值得注意的是,与相应的雄性小鼠相比,雌性 hAβ-KI 和 APP-KI 小鼠的认知障碍更为明显。我们的研究结果表明,Aβ 人源化导致 APP-KI 小鼠的认知缺陷,淀粉样蛋白沉积与 APP-KI 小鼠的认知障碍可能没有密切关联。