Marottoli Felecia M, Balu Deebika, Flores-Barrera Eden, de la Villarmois Emilce Artur, Zhang Hui, Chaudhary Rohan, Talati Ruju, Tseng Kuei Y, Tai Leon M
Department of Anatomy and Cell Biology University of Illinois at Chicago Chicago IL USA.
J Am Heart Assoc. 2024 Dec 3;13(23):e035080. doi: 10.1161/JAHA.124.035080. Epub 2024 Nov 29.
We recently found that loss of endothelial cell disrupts neurovascular and synaptic function. However, whether endothelial is detrimental or protective for neural function under physiological conditions is unknown. Therefore, the goal of this study was to determine the role of endothelial cell in regulating brain function in vivo.
We developed /Cdh5(PAC)-CreERT2 and /Cdh5(PAC)-CreERT2 (control) mice. Knockdown of endothelial cell was induced at ≈4 to 5 weeks of age. Experiments were conducted at 9 months of age to evaluate neurovascular and neuronal function via biochemistry, immunohistochemistry, behavior tests, and electrophysiology. Endothelial cell knockdown resulted in higher neurovascular permeability, lower claudin-5 vessel coverage, impaired trace fear memory extinction, and disruption of cortical excitatory-inhibitory balance of synaptic activity.
Our data support the novel concept that endothelial cell is protective for brain function when other cell types express .
我们最近发现内皮细胞缺失会破坏神经血管和突触功能。然而,在生理条件下内皮细胞对神经功能是有害还是具有保护作用尚不清楚。因此,本研究的目的是确定内皮细胞在体内调节脑功能中的作用。
我们培育了/Cdh5(PAC)-CreERT2和/Cdh5(PAC)-CreERT2(对照)小鼠。在约4至5周龄时诱导内皮细胞缺失。在9月龄时进行实验,通过生物化学、免疫组织化学、行为测试和电生理学评估神经血管和神经元功能。内皮细胞缺失导致神经血管通透性增加、紧密连接蛋白-5血管覆盖率降低、痕迹恐惧记忆消退受损以及突触活动的皮质兴奋性-抑制性平衡破坏。
我们的数据支持了一个新的概念,即当其他细胞类型表达时,内皮细胞对脑功能具有保护作用。