Intramural hematomas and astrocytic infiltration precede perivascular inflammation in a rat model of repetitive low-level blast injury.

IF 3 3区 医学 Q2 CLINICAL NEUROLOGY
Miguel A Gama Sosa, Rita De Gasperi, Rachel H Lind, Dylan Pryor, Danielle C Vargas, Georgina S Perez Garcia, Gissel M Perez, Rania Abutarboush, Usmah Kawoos, Allison Sowa, Carolyn W Zhu, William G M Janssen, Patrick R Hof, Stephen T Ahlers, Gregory A Elder
{"title":"Intramural hematomas and astrocytic infiltration precede perivascular inflammation in a rat model of repetitive low-level blast injury.","authors":"Miguel A Gama Sosa, Rita De Gasperi, Rachel H Lind, Dylan Pryor, Danielle C Vargas, Georgina S Perez Garcia, Gissel M Perez, Rania Abutarboush, Usmah Kawoos, Allison Sowa, Carolyn W Zhu, William G M Janssen, Patrick R Hof, Stephen T Ahlers, Gregory A Elder","doi":"10.1093/jnen/nlaf003","DOIUrl":null,"url":null,"abstract":"<p><p>In modern war theaters, exposures to blast overpressures are one of the most common causes of brain injury. These pervasive events result in acute and chronic cerebrovascular degenerative processes. Using a rat model of blast-induced mild traumatic brain injury, we identified intramural periarterial hematomas as early primary acute lesions induced by blast exposures. These lesions resulted in intravascular cell death, cell layer reorganization, and plasma leakage into the intraperiarterial basal membranes that constitute the intraperiarterial drainage system (IPAD). Plasma metalloproteases, including MMP-9, in the IPAD basal membranes may degrade extracellular matrix components compromising normal cerebral interstitial fluid drainage, arterial structure and function leading to chronic vascular degenerative processes. Related subacute effects of blast exposure included increased MMP-9 expression in perivascular reactive astrocytes and the extension of astrocytic processes through the layers of affected vessels. These results, in combination with normal levels of proinflammatory cytokines and the absence of proinflammatory MHC II-expressing microglia, suggest an astrocytic role in the clearing of intravascular hematomas and provide further mechanistic evidence that blast-induced vascular degenerative processes may precede the onset of neurovascular inflammation.</p>","PeriodicalId":16682,"journal":{"name":"Journal of Neuropathology and Experimental Neurology","volume":" ","pages":"337-352"},"PeriodicalIF":3.0000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11923744/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Neuropathology and Experimental Neurology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/jnen/nlaf003","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

In modern war theaters, exposures to blast overpressures are one of the most common causes of brain injury. These pervasive events result in acute and chronic cerebrovascular degenerative processes. Using a rat model of blast-induced mild traumatic brain injury, we identified intramural periarterial hematomas as early primary acute lesions induced by blast exposures. These lesions resulted in intravascular cell death, cell layer reorganization, and plasma leakage into the intraperiarterial basal membranes that constitute the intraperiarterial drainage system (IPAD). Plasma metalloproteases, including MMP-9, in the IPAD basal membranes may degrade extracellular matrix components compromising normal cerebral interstitial fluid drainage, arterial structure and function leading to chronic vascular degenerative processes. Related subacute effects of blast exposure included increased MMP-9 expression in perivascular reactive astrocytes and the extension of astrocytic processes through the layers of affected vessels. These results, in combination with normal levels of proinflammatory cytokines and the absence of proinflammatory MHC II-expressing microglia, suggest an astrocytic role in the clearing of intravascular hematomas and provide further mechanistic evidence that blast-induced vascular degenerative processes may precede the onset of neurovascular inflammation.

在大鼠重复性低水平爆炸损伤模型中,壁内血肿和星形细胞浸润先于血管周围炎症。
在现代战场上,暴露在爆炸超压下是造成脑损伤最常见的原因之一。这些普遍的事件导致急性和慢性脑血管退行性过程。利用爆炸引起的轻度创伤性脑损伤大鼠模型,我们确定了壁内动脉周围血肿是爆炸暴露引起的早期原发性急性病变。这些病变导致血管内细胞死亡、细胞层重组和血浆渗漏到构成动脉内引流系统(IPAD)的动脉内基底膜。血浆金属蛋白酶,包括IPAD基膜中的MMP-9,可降解细胞外基质成分,影响正常的脑间质液引流、动脉结构和功能,导致慢性血管退行性过程。爆炸暴露的相关亚急性效应包括血管周围反应性星形胶质细胞中MMP-9表达的增加以及星形胶质细胞过程通过受影响血管层的延伸。这些结果,结合正常水平的促炎细胞因子和缺乏表达促炎MHC ii的小胶质细胞,提示星形胶质细胞在清除血管内血肿中的作用,并提供进一步的机制证据,表明爆炸诱导的血管退行性过程可能先于神经血管炎症的发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
5.40
自引率
6.20%
发文量
118
审稿时长
6-12 weeks
期刊介绍: Journal of Neuropathology & Experimental Neurology is the official journal of the American Association of Neuropathologists, Inc. (AANP). The journal publishes peer-reviewed studies on neuropathology and experimental neuroscience, book reviews, letters, and Association news, covering a broad spectrum of fields in basic neuroscience with an emphasis on human neurological diseases. It is written by and for neuropathologists, neurologists, neurosurgeons, pathologists, psychiatrists, and basic neuroscientists from around the world. Publication has been continuous since 1942.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信