Endothelial Cell APOE3 Regulates Neurovascular, Neuronal, and Behavioral Function

BACKGROUND: Specialized brain endothelial cells and human APOE3 are independently important for neurovascular function, yet whether APOE3 expression by endothelial cells contributes to brain function is currently unknown. In the present study, we determined whether the loss of endothelial cell APOE3 impacts brain vascular and neural function. METHODS: We developed APOE3(fl/fl)/Cdh5(PAC)-CreERT2(+/-) (APOE3(Cre+/-)) and APOE3(fl/fl)/Cdh5(PAC)-CreERT2(-/-)(APOE3(Cre-/-), control) mice and induced endothelial cell APOE3 knockdown with tamoxifen at approximate to 4 to 5 weeks of age. Neurovascular and neuronal function were evaluated by biochemistry, immunohistochemistry, behavioral testing, and electrophysiology at 9 months of age. RESULTS: We found that the loss of endothelial APOE3 expression was sufficient to cause neurovascular dysfunction including higher permeability and lower vessel coverage in tandem with deficits in spatial memory and fear memory extinction and a disruption of cortical excitatory/inhibitory balance. CONCLUSIONS: Our data collectively support the novel concept that endothelial APOE3 plays a critical role in the regulation of the neurovasculature, neural circuit function, and behavior.

Automated summary

The loss of endothelial cell APOE3 expression leads to neurovascular dysfunction and abnormalities in neural function. This finding supports the importance of endothelial cell APOE3 in neurovascular regulation, neural circuit function, and behavior.