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内皮细胞调节神经血管、神经元和行为功能。

Endothelial Cell Regulates Neurovascular, Neuronal, and Behavioral Function.

机构信息

Departments of Anatomy and Cell Biology (F.M.M., H.Z., E.F.-B., E.A.d.l.V., A.M.M.M.F., H.V.B., R.C., A.L.N., A.E.N., R.T., A.S.J., K.M., S.E.L., K.Y.T., L.M.T.), University of Illinois at Chicago.

Radiology (F.C.D., K.C.), University of Illinois at Chicago.

出版信息

Arterioscler Thromb Vasc Biol. 2023 Oct;43(10):1952-1966. doi: 10.1161/ATVBAHA.123.319816. Epub 2023 Aug 31.

Abstract

BACKGROUND

Specialized brain endothelial cells and human are independently important for neurovascular function, yet whether expression by endothelial cells contributes to brain function is currently unknown. In the present study, we determined whether the loss of endothelial cell impacts brain vascular and neural function.

METHODS

We developed /Cdh5(PAC)-CreERT2 () and /Cdh5(PAC)-CreERT2 (, control) mice and induced endothelial cell knockdown with tamoxifen at ≈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 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 plays a critical role in the regulation of the neurovasculature, neural circuit function, and behavior.

摘要

背景

专门的脑内皮细胞和人对于神经血管功能是独立重要的,然而内皮细胞表达是否有助于大脑功能目前尚不清楚。在本研究中,我们确定了内皮细胞中 的缺失是否会影响脑血管和神经功能。

方法

我们开发了 /Cdh5(PAC)-CreERT2 () 和 /Cdh5(PAC)-CreERT2 (,对照) 小鼠,并在约 4 到 5 周龄时用他莫昔芬诱导内皮细胞 敲低。在 9 个月大时,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。

结果

我们发现内皮细胞 表达的缺失足以导致神经血管功能障碍,包括通透性增加、血管覆盖率降低,同时伴有空间记忆和恐惧记忆消退缺陷,以及皮质兴奋性/抑制性平衡破坏。

结论

我们的数据共同支持内皮细胞 对于神经血管、神经回路功能和行为的调节起着关键作用的新观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d32/10521805/89b9b4e57a5b/atv-43-1952-g001.jpg

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