Cytokines regulate IGF binding proteins in the CNS

Teresa L. Wood, Steven L. O'Donnell, Steven W. Levison
{"title":"Cytokines regulate IGF binding proteins in the CNS","authors":"Teresa L. Wood,&nbsp;Steven L. O'Donnell,&nbsp;Steven W. Levison","doi":"10.1016/0955-2235(95)00035-6","DOIUrl":null,"url":null,"abstract":"<div><p>Growth factor induction is a major component of the response to central nervous system trauma. The insulin-like growth factors (IGFs) and IGF binding proteins (IGFBPs) are among the molecules induced by injury that have demonstrated neuroprotective actions. Induction of IGFBPs 2, 3, 4 and 5 have been documented following injury and are hypothesized to function in transport or localization of the IGFs to injured cells. It is unclear what factors lead to induction of these molecules following trauma, however, several cytokines including ciliary neurotrophic factor (CNTF) and interleukin-1β (IL-1β) have been described as major injury signals and can induce aspects of reactive gliosis. To establish whether these cytokines also are responsible for inducing the IGFBPs following CNS injury, we injected CNTF or IL-1β intracerebrally into the neocortex of adult rats and measured changes in mRNA expression for the IGFBPs. IGFBP-2 mRNA showed a dramatic increase by 24–48 h following either CNTF or IL-1β injection as compared with the contralateral side injected with heat-inactivated cytokine. Neither CNTF nor IL-1β caused alterations in BP3 or BP5. Levels of BP4 and BP6 mRNAs also were unchanged following CNTF injection. These results suggest that IGFBP2 is uniquely regulated among the IGFBPs in the CNS and is induced by cytokines that signal CNS injury.</p></div>","PeriodicalId":77335,"journal":{"name":"Progress in growth factor research","volume":"6 2","pages":"Pages 181-187"},"PeriodicalIF":0.0000,"publicationDate":"1995-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0955-2235(95)00035-6","citationCount":"18","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Progress in growth factor research","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0955223595000356","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 18

Abstract

Growth factor induction is a major component of the response to central nervous system trauma. The insulin-like growth factors (IGFs) and IGF binding proteins (IGFBPs) are among the molecules induced by injury that have demonstrated neuroprotective actions. Induction of IGFBPs 2, 3, 4 and 5 have been documented following injury and are hypothesized to function in transport or localization of the IGFs to injured cells. It is unclear what factors lead to induction of these molecules following trauma, however, several cytokines including ciliary neurotrophic factor (CNTF) and interleukin-1β (IL-1β) have been described as major injury signals and can induce aspects of reactive gliosis. To establish whether these cytokines also are responsible for inducing the IGFBPs following CNS injury, we injected CNTF or IL-1β intracerebrally into the neocortex of adult rats and measured changes in mRNA expression for the IGFBPs. IGFBP-2 mRNA showed a dramatic increase by 24–48 h following either CNTF or IL-1β injection as compared with the contralateral side injected with heat-inactivated cytokine. Neither CNTF nor IL-1β caused alterations in BP3 or BP5. Levels of BP4 and BP6 mRNAs also were unchanged following CNTF injection. These results suggest that IGFBP2 is uniquely regulated among the IGFBPs in the CNS and is induced by cytokines that signal CNS injury.

细胞因子调节中枢神经系统中的IGF结合蛋白
生长因子诱导是中枢神经系统创伤反应的主要组成部分。胰岛素样生长因子(IGF)和IGF结合蛋白(igfbp)是损伤诱导的具有神经保护作用的分子。损伤后igfbp 2、3、4和5的诱导已被证实,并被推测在IGFs向损伤细胞的运输或定位中起作用。目前尚不清楚是什么因素导致创伤后这些分子的诱导,然而,包括睫状体神经营养因子(CNTF)和白细胞介素-1β (IL-1β)在内的几种细胞因子已被描述为主要的损伤信号,并可诱导反应性胶质细胞增生。为了确定这些细胞因子是否也负责诱导中枢神经系统损伤后的igfbp,我们将CNTF或IL-1β注入成年大鼠的脑内新皮层,并测量igfbp mRNA表达的变化。与对侧注射热灭活细胞因子相比,注射CNTF或IL-1β后24-48小时IGFBP-2 mRNA显著增加。CNTF和IL-1β均未引起BP3或BP5的改变。注射CNTF后,BP4和BP6 mrna的水平也没有变化。这些结果表明,IGFBP2在中枢神经系统的igfbp中受到独特的调控,并由信号中枢神经系统损伤的细胞因子诱导。
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
自引率
0.00%
发文量
0
×
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:481959085
Book学术官方微信