18 kDa转运蛋白与非痴呆老年人海马小胶质细胞有关

IF 1.7 Q3 CLINICAL NEUROLOGY Aging brain Pub Date : 2022-01-01 DOI:10.1016/j.nbas.2022.100045
Benjamin B. Tournier , Christophe Snoeijs , Stergios Tsartsalis , Quentin Amossé , Ramzi Farchoukh , Eniko Kövari , Kelly Ceyzériat , Philippe Millet
{"title":"18 kDa转运蛋白与非痴呆老年人海马小胶质细胞有关","authors":"Benjamin B. Tournier ,&nbsp;Christophe Snoeijs ,&nbsp;Stergios Tsartsalis ,&nbsp;Quentin Amossé ,&nbsp;Ramzi Farchoukh ,&nbsp;Eniko Kövari ,&nbsp;Kelly Ceyzériat ,&nbsp;Philippe Millet","doi":"10.1016/j.nbas.2022.100045","DOIUrl":null,"url":null,"abstract":"<div><p>Increase in the brain expression of the 18 kDa translocator protein (TSPO) is considered as a marker of neuroinflammation in the context of brain diseases, such as Alzheimer’s disease (AD). However, in non-demented subjects with Alzheimer’s neuropathology, TSPO accumulation in hippocampus subdivisions has not been fully characterized.</p><p>To determine if TSPO is associated with the presence of amyloid β plaques and/or phosphorylated Tau accumulation, we analyzed hippocampal sections using immunohistochemistry of 14 non-demented subjects with positive staining for Aβ and/or phosphorylated Tau. TSPO expression was heterogenous with higher accumulation in the CA2/3 and subiculum subfields of the hippocampus. Its distribution closely resembled that of the microglial IBA1 marker and of the Aβ42 amyloid form. In addition, positive correlations were observed between TSPO and IBA1 densities in CA4, CA2/3 and the subiculum but not with either the astrocyte GFAP marker or the AD-type Aβ and Tau markers. This study sustains the hypothesis that TSPO is mainly associated with microglia and in Aβ42-rich subdivisions in the hippocampus of non-demented elderly individuals.</p></div>","PeriodicalId":72131,"journal":{"name":"Aging brain","volume":"2 ","pages":"Article 100045"},"PeriodicalIF":1.7000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/f6/e3/main.PMC9997180.pdf","citationCount":"0","resultStr":"{\"title\":\"The 18 kDa translocator protein is associated with microglia in the hippocampus of non-demented elderly subjects\",\"authors\":\"Benjamin B. Tournier ,&nbsp;Christophe Snoeijs ,&nbsp;Stergios Tsartsalis ,&nbsp;Quentin Amossé ,&nbsp;Ramzi Farchoukh ,&nbsp;Eniko Kövari ,&nbsp;Kelly Ceyzériat ,&nbsp;Philippe Millet\",\"doi\":\"10.1016/j.nbas.2022.100045\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Increase in the brain expression of the 18 kDa translocator protein (TSPO) is considered as a marker of neuroinflammation in the context of brain diseases, such as Alzheimer’s disease (AD). However, in non-demented subjects with Alzheimer’s neuropathology, TSPO accumulation in hippocampus subdivisions has not been fully characterized.</p><p>To determine if TSPO is associated with the presence of amyloid β plaques and/or phosphorylated Tau accumulation, we analyzed hippocampal sections using immunohistochemistry of 14 non-demented subjects with positive staining for Aβ and/or phosphorylated Tau. TSPO expression was heterogenous with higher accumulation in the CA2/3 and subiculum subfields of the hippocampus. Its distribution closely resembled that of the microglial IBA1 marker and of the Aβ42 amyloid form. In addition, positive correlations were observed between TSPO and IBA1 densities in CA4, CA2/3 and the subiculum but not with either the astrocyte GFAP marker or the AD-type Aβ and Tau markers. This study sustains the hypothesis that TSPO is mainly associated with microglia and in Aβ42-rich subdivisions in the hippocampus of non-demented elderly individuals.</p></div>\",\"PeriodicalId\":72131,\"journal\":{\"name\":\"Aging brain\",\"volume\":\"2 \",\"pages\":\"Article 100045\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/f6/e3/main.PMC9997180.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Aging brain\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2589958922000172\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Aging brain","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2589958922000172","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

摘要

脑部18 kDa转运蛋白(TSPO)表达的增加被认为是脑疾病(如阿尔茨海默病(AD))背景下神经炎症的标志物。然而,在患有阿尔茨海默病的非痴呆受试者中,TSPO在海马体分支中的积累尚未得到充分表征。为了确定TSPO是否与β淀粉样蛋白斑块和/或磷酸化Tau积累有关,我们使用免疫组织化学分析了14名非痴呆受试者的海马切片,这些受试者的Aβ和/或磷酸化Tau染色呈阳性。TSPO表达具有异质性,在海马CA2/3和托下亚区有较高的积累。它的分布与小胶质IBA1标记物和Aβ42淀粉样蛋白形式非常相似。此外,CA4、CA2/3和骨下的TSPO和IBA1密度呈正相关,但与星形胶质细胞GFAP标记物或ad型Aβ和Tau标记物均无正相关。本研究支持了TSPO主要与非痴呆老年人海马中小胶质细胞和富含a β42的分支相关的假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
The 18 kDa translocator protein is associated with microglia in the hippocampus of non-demented elderly subjects

Increase in the brain expression of the 18 kDa translocator protein (TSPO) is considered as a marker of neuroinflammation in the context of brain diseases, such as Alzheimer’s disease (AD). However, in non-demented subjects with Alzheimer’s neuropathology, TSPO accumulation in hippocampus subdivisions has not been fully characterized.

To determine if TSPO is associated with the presence of amyloid β plaques and/or phosphorylated Tau accumulation, we analyzed hippocampal sections using immunohistochemistry of 14 non-demented subjects with positive staining for Aβ and/or phosphorylated Tau. TSPO expression was heterogenous with higher accumulation in the CA2/3 and subiculum subfields of the hippocampus. Its distribution closely resembled that of the microglial IBA1 marker and of the Aβ42 amyloid form. In addition, positive correlations were observed between TSPO and IBA1 densities in CA4, CA2/3 and the subiculum but not with either the astrocyte GFAP marker or the AD-type Aβ and Tau markers. This study sustains the hypothesis that TSPO is mainly associated with microglia and in Aβ42-rich subdivisions in the hippocampus of non-demented elderly individuals.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Aging brain
Aging brain Neuroscience (General), Geriatrics and Gerontology
自引率
0.00%
发文量
0
期刊最新文献
Age-related differences in structural and resting-state functional brain network organization across the adult lifespan: A cross-sectional study Age-related fornix decline predicts conservative response strategy-based slowing in perceptual decision-making Age-related decline in social interaction is associated with decreased c-Fos induction in select brain regions independent of oxytocin receptor expression profiles Innate immunity in brain aging and neurodegeneration Neural correlates of home-based intervention effects on value-based sequential decision-making in healthy older adults
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1