Journal Article

Peripheral apoE4 enhances Alzheimer’s pathology and impairs cognition by compromising cerebrovascular function

Fu, Yuan, Liu, Chia-Chen, Wang, Zhen, Bastea, Ligia, Rogers, Justin, Wang, Minghui, Quicksall, Zachary S, Kuchenbecker, Lindsey A, Kanekiyo, Takahisa, Felton, Lindsey, Asmann, Yan W, Rosenberg, Cassandra L, Wang, Xusheng, Bu, Guojun, Chen, Yuanxin, Linares, Cynthia, Jia, Lin, Wang, Na, Yamazaki, Akari, Kong, Dehui, Trottier, Zachary A, Chen, Yixing, Doss, Sydney V, Qiao, Wenhui, Kurti, Aishe, Inoue, Yasuteru, Yamazaki, Yu, Peng, Junmin, Zhao, Na, Kim, Betty Y. S, Shue, Francis, Li, Zonghua, Knight, Joshua, Fryer, John D, Zhao, Jing, Zhang, Bin, Storz, Peter, Ren, Yingxue, Jeevaratnam, Suren, Martens, Yuka A

2022

Overview

The ε4 allele of the apolipoprotein E (APOE) gene, a genetic risk factor for Alzheimer’s disease, is abundantly expressed in both the brain and periphery. Here, we present evidence that peripheral apoE isoforms, separated from those in the brain by the blood–brain barrier, differentially impact Alzheimer’s disease pathogenesis and cognition. To evaluate the function of peripheral apoE, we developed conditional mouse models expressing human APOE3 or APOE4 in the liver with no detectable apoE in the brain. Liver-expressed apoE4 compromised synaptic plasticity and cognition by impairing cerebrovascular functions. Plasma proteome profiling revealed apoE isoform-dependent functional pathways highlighting cell adhesion, lipoprotein metabolism and complement activation. ApoE3 plasma from young mice improved cognition and reduced vessel-associated gliosis when transfused into aged mice, whereas apoE4 compromised the beneficial effects of young plasma. A human induced pluripotent stem cell-derived endothelial cell model recapitulated the plasma apoE isoform-specific effect on endothelial integrity, further supporting a vascular-related mechanism. Upon breeding with amyloid model mice, liver-expressed apoE4 exacerbated brain amyloid pathology, whereas apoE3 reduced it. Our findings demonstrate pathogenic effects of peripheral apoE4, providing a strong rationale for targeting peripheral apoE to treat Alzheimer’s disease.Mouse models expressing liver apoE in the absence of brain apoE reveal detrimental effects of peripheral apoE4 associated with Alzheimer’s risk on cognition and amyloid pathology through compromising vascular integrity and function.

• Publisher: Nature Publishing Group
• Subject: Alzheimer's disease / Animal models / Apolipoprotein E / Apolipoprotein E4 / Blood vessels / Blood-brain barrier / Cell adhesion / Cognition / Cognition & reasoning / Complement activation / Endothelial cells / Functionals / Gliosis / Integrity / Isoforms / Lipid metabolism / Liver / Liver diseases / Neurodegenerative diseases / Pathogenesis / Pathology / Plasma / Pluripotency / Proteomes / Risk analysis / Risk factors / Stem cells / Synaptic plasticity