Transforming Growth Factor-β: Neuronal and Glial Expression in CNS Degenerative Diseases

Carol F. Lippa , Thomas W. Smith , Kathleen C. Flanders
{"title":"Transforming Growth Factor-β: Neuronal and Glial Expression in CNS Degenerative Diseases","authors":"Carol F. Lippa ,&nbsp;Thomas W. Smith ,&nbsp;Kathleen C. Flanders","doi":"10.1006/neur.1995.0051","DOIUrl":null,"url":null,"abstract":"<div><p>We have previously shown that the brains of patients with Alzheimer's disease (AD) express transforming growth factor (TGF)-β2 in neurofibrillary tangle (NFT) -bearing neurons and reactive astrocytes. The present study was undertaken to determine whether other neurodegenerative diseases were also associated with an alteration of the TGF-β's. The immunohistochemical expression of TGF-β1, -2 and -3 was assessed in the brains of patients with progressive supranuclear palsy (<em>n</em>=2), amyotrophic lateral sclerosis (<em>n</em>=3), Lewy body disease (<em>n</em>=5), Parkinson's disease (<em>n</em>=1), Shy-Drager syndrome (<em>n</em>=1), Pick's disease (<em>n</em>=3), lobar atrophy (<em>n</em>=1), and corticobasal degeneration (<em>n</em>=2). Our results were compared to norms for controls (<em>n</em>=8). We found expression of TGF-β2 in both NFT bearing neurons and tangle-bearing glial cells in progressive supranuclear palsy and in neurons with age-related NFT formation. Widespread staining of reactive astrocytes for TGF-β2 was observed in all degenerative diseases. TGF-β1 and -3 staining was not selectively altered in these diseases. We conclude that induction of TGF-β2 may be an intrinsic part of the processes that underlie NFT formation and reactive gliosis in a variety of neurodegenerative diseases.</p></div>","PeriodicalId":19127,"journal":{"name":"Neurodegeneration","volume":"4 4","pages":"Pages 425-432"},"PeriodicalIF":0.0000,"publicationDate":"1995-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1006/neur.1995.0051","citationCount":"44","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurodegeneration","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1055833085700517","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 44

Abstract

We have previously shown that the brains of patients with Alzheimer's disease (AD) express transforming growth factor (TGF)-β2 in neurofibrillary tangle (NFT) -bearing neurons and reactive astrocytes. The present study was undertaken to determine whether other neurodegenerative diseases were also associated with an alteration of the TGF-β's. The immunohistochemical expression of TGF-β1, -2 and -3 was assessed in the brains of patients with progressive supranuclear palsy (n=2), amyotrophic lateral sclerosis (n=3), Lewy body disease (n=5), Parkinson's disease (n=1), Shy-Drager syndrome (n=1), Pick's disease (n=3), lobar atrophy (n=1), and corticobasal degeneration (n=2). Our results were compared to norms for controls (n=8). We found expression of TGF-β2 in both NFT bearing neurons and tangle-bearing glial cells in progressive supranuclear palsy and in neurons with age-related NFT formation. Widespread staining of reactive astrocytes for TGF-β2 was observed in all degenerative diseases. TGF-β1 and -3 staining was not selectively altered in these diseases. We conclude that induction of TGF-β2 may be an intrinsic part of the processes that underlie NFT formation and reactive gliosis in a variety of neurodegenerative diseases.

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
转化生长因子-β:中枢神经系统退行性疾病中的神经元和胶质表达
我们之前的研究表明,阿尔茨海默病(AD)患者的大脑在神经原纤维缠结(NFT)神经元和反应性星形胶质细胞中表达转化生长因子(TGF)-β2。本研究旨在确定其他神经退行性疾病是否也与TGF-β的改变有关。在进行性核上性麻痹(n=2)、肌萎缩性侧索硬化症(n=3)、路易斯体病(n=5)、帕金森病(n=1)、希-德尔格综合征(n=1)、匹克病(n=3)、脑叶萎缩(n=1)、皮质基底退行性变(n=2)患者的大脑中检测TGF-β1、-2和-3的免疫组化表达。将我们的结果与对照组的标准进行比较(n=8)。我们发现TGF-β2在进行性核上麻痹的NFT神经元和缠结胶质细胞中表达,并在与年龄相关的NFT形成的神经元中表达。在所有退行性疾病中均可见TGF-β2反应性星形细胞的广泛染色。TGF-β1和-3染色在这些疾病中没有选择性改变。我们得出结论,TGF-β2的诱导可能是多种神经退行性疾病中NFT形成和反应性胶质瘤形成过程的内在组成部分。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Behavioural Problems in Dementia and Biochemistry: Clinical Aspects Neurochemical Correlates of Dementia Amyloid Precursor Protein mRNAs in Alzheimer's Disease Structural Correlates of Cognition in Dementia: Quantification and Assessment of Synapse Change Pyramidal Nerve Cell Loss in Alzheimer's Disease
×
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