低强度露天爆破对小鼠神经血管单位超微结构的影响。

IF 6.2 2区 医学 Q1 NEUROSCIENCES Acta Neuropathologica Communications Pub Date : 2023-09-06 DOI:10.1186/s40478-023-01636-4
Chao Li, Shanyan Chen, Heather R Siedhoff, DeAna Grant, Pei Liu, Ashley Balderrama, Marcus Jackson, Amitai Zuckerman, C Michael Greenlief, Firas Kobeissy, Kevin W Wang, Ralph G DePalma, Ibolja Cernak, Jiankun Cui, Zezong Gu
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引用次数: 0

摘要

低强度爆炸(LIB)引起的轻度创伤性脑损伤(mTBI)是影响军人和退伍军人的严重健康问题。我们之前使用单个开放场LIB小鼠模型的报告显示,大脑中没有严重的显微镜损伤或坏死,而透射电子显微镜(TEM)则发现髓鞘、线粒体和突触的超微结构异常。神经血管单元(NVU)是一个由多个组成部分组成的解剖和功能系统,对调节大脑血流和细胞相互作用至关重要。在这项研究中,我们定量和定性地描述了影响LIB暴露小鼠NVU的超微结构异常。在损伤后7天(DPI)发现管腔收缩不规则性,随后在30DPI时扩张并伴有周细胞变性。定量蛋白质组学分析鉴定了损伤后24小时血管舒缩相关蛋白的显著改变。暴露于LIB的小鼠出现内皮细胞、基底膜和星形胶质细胞端足肿胀以及液泡形成,表明细胞水肿。还注意到紧密连接的结构异常和星形胶质细胞末端足从基底膜脱离。这些超微结构发现表明LIB诱导多组分NVU损伤。预防NVU损伤可能有助于确定治疗靶点,以减轻原发性脑爆炸损伤的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Low-intensity open-field blast exposure effects on neurovascular unit ultrastructure in mice.

Mild traumatic brain injury (mTBI) induced by low-intensity blast (LIB) is a serious health problem affecting military service members and veterans. Our previous reports using a single open-field LIB mouse model showed the absence of gross microscopic damage or necrosis in the brain, while transmission electron microscopy (TEM) identified ultrastructural abnormalities of myelin sheaths, mitochondria, and synapses. The neurovascular unit (NVU), an anatomical and functional system with multiple components, is vital for the regulation of cerebral blood flow and cellular interactions. In this study, we delineated ultrastructural abnormalities affecting the NVU in mice with LIB exposure quantitatively and qualitatively. Luminal constrictive irregularities were identified at 7 days post-injury (DPI) followed by dilation at 30 DPI along with degeneration of pericytes. Quantitative proteomic analysis identified significantly altered vasomotor-related proteins at 24 h post-injury. Endothelial cell, basement membrane and astrocyte end-foot swellings, as well as vacuole formations, occurred in LIB-exposed mice, indicating cellular edema. Structural abnormalities of tight junctions and astrocyte end-foot detachment from basement membranes were also noted. These ultrastructural findings demonstrate that LIB induces multiple-component NVU damage. Prevention of NVU damage may aid in identifying therapeutic targets to mitigate the effects of primary brain blast injury.

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来源期刊
Acta Neuropathologica Communications
Acta Neuropathologica Communications Medicine-Pathology and Forensic Medicine
CiteScore
11.20
自引率
2.80%
发文量
162
审稿时长
8 weeks
期刊介绍: "Acta Neuropathologica Communications (ANC)" is a peer-reviewed journal that specializes in the rapid publication of research articles focused on the mechanisms underlying neurological diseases. The journal emphasizes the use of molecular, cellular, and morphological techniques applied to experimental or human tissues to investigate the pathogenesis of neurological disorders. ANC is committed to a fast-track publication process, aiming to publish accepted manuscripts within two months of submission. This expedited timeline is designed to ensure that the latest findings in neuroscience and pathology are disseminated quickly to the scientific community, fostering rapid advancements in the field of neurology and neuroscience. The journal's focus on cutting-edge research and its swift publication schedule make it a valuable resource for researchers, clinicians, and other professionals interested in the study and treatment of neurological conditions.
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