Adesewa O Akande, Zachary A Carter, Karen Y Stokes, Hyung W Nam
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Deletion of Ng significantly decreases neurovascular density in mice. Using in vivo permeability assays, we found increased neurovascular permeability in Ng null mice. We also observed significant changes in the expression of tight junction proteins using western blot and immunofluorescent staining. To identify the molecular pathways involved, we carried out label-free proteomics on brain lysates from endothelial-specific Ng knockout mice. Ingenuity Pathway Analysis indicated that the AKT pathway is attenuated in the vasculature of endothelial-specific Ng knockout mice. To validate these in vivo findings, we pharmacologically manipulated AKT signaling in hCMEC/D3 cells and observed that inhibition of AKT activation causes increased permeability. Our results indicate that the loss of Ng expression alters neurovascular structure and permeability, potentially contributing to neurological dysfunction. 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引用次数: 0
摘要
神经粒蛋白(Ng)的表达是阿尔茨海默病的生物标志物。大脑中 Ng 的减少和 CSF 中 Ng 的增加与认知能力的下降呈正相关。众所周知,Ng能调节神经元的钙-钙调蛋白结合和突触可塑性,这对学习/记忆至关重要。有趣的是,我们发现 Ng 也在小鼠和人类血脑屏障(BBB)中表达。然而,Ng在脑血管中的表达作用在很大程度上仍未确定。在这项研究中,我们利用 Ng 基因缺失小鼠和人脑微血管内皮细胞(hCMEC/D3)研究了 Ng 表达对神经血管结构和功能的作用。我们对全脑和脑切片的血管进行了清脑和免疫标记。Ng缺失会明显降低小鼠的神经血管密度。通过体内通透性试验,我们发现 Ng 基因缺失小鼠的神经血管通透性增加。我们还利用 Western 印迹和免疫荧光染色观察到紧密连接蛋白的表达发生了显著变化。为了确定所涉及的分子通路,我们对内皮特异性 Ng 基因敲除小鼠的脑裂解物进行了无标记蛋白质组学研究。Ingenuity Pathway 分析表明,在内皮特异性 Ng 基因敲除小鼠的血管中,AKT 通路的作用减弱。为了验证这些体内研究结果,我们对 hCMEC/D3 细胞中的 AKT 信号进行了药理学处理,并观察到抑制 AKT 激活会导致通透性增加。我们的研究结果表明,Ng表达的缺失会改变神经血管结构和通透性,从而可能导致神经功能障碍。因此,调节 Ng 在 BBB 中的表达可为阿尔茨海默病提供一种新的治疗方法。
Endothelial Neurogranin Regulates Blood-Brain Barrier Permeability via Modulation of the AKT Pathway.
Neurogranin (Ng) expression is a biomarker for Alzheimer's disease. A loss of brain Ng and an increase in CSF Ng positively correlate with cognitive decline. Ng is known to regulate neuronal calcium-calmodulin binding and synaptic plasticity, which are critical for learning/memory. Interestingly, we discovered that Ng is also expressed in mouse and human blood-brain barrier (BBB). However, the role of Ng expression in brain vasculature remains largely undefined. In this study, we investigated the role of Ng expression on neurovascular structure and function using Ng null mice and human cerebral microvascular endothelial (hCMEC/D3) cells. We performed brain clearing and immunolabeling of blood vessels from whole brains and brain slices. Deletion of Ng significantly decreases neurovascular density in mice. Using in vivo permeability assays, we found increased neurovascular permeability in Ng null mice. We also observed significant changes in the expression of tight junction proteins using western blot and immunofluorescent staining. To identify the molecular pathways involved, we carried out label-free proteomics on brain lysates from endothelial-specific Ng knockout mice. Ingenuity Pathway Analysis indicated that the AKT pathway is attenuated in the vasculature of endothelial-specific Ng knockout mice. To validate these in vivo findings, we pharmacologically manipulated AKT signaling in hCMEC/D3 cells and observed that inhibition of AKT activation causes increased permeability. Our results indicate that the loss of Ng expression alters neurovascular structure and permeability, potentially contributing to neurological dysfunction. Therefore, modulating Ng expression in the BBB may offer a novel therapeutic approach for Alzheimer's disease.
期刊介绍:
Molecular Neurobiology is an exciting journal for neuroscientists needing to stay in close touch with progress at the forefront of molecular brain research today. It is an especially important periodical for graduate students and "postdocs," specifically designed to synthesize and critically assess research trends for all neuroscientists hoping to stay active at the cutting edge of this dramatically developing area. This journal has proven to be crucial in departmental libraries, serving as essential reading for every committed neuroscientist who is striving to keep abreast of all rapid developments in a forefront field. Most recent significant advances in experimental and clinical neuroscience have been occurring at the molecular level. Until now, there has been no journal devoted to looking closely at this fragmented literature in a critical, coherent fashion. Each submission is thoroughly analyzed by scientists and clinicians internationally renowned for their special competence in the areas treated.