Glial cell response to constant low light exposure in rat retina.

IF 1.1 4区 医学 Q4 NEUROSCIENCES Visual Neuroscience Pub Date : 2022-09-27 DOI:10.1017/S0952523822000049
Manuel G Bruera, María M Benedetto, Mario E Guido, Alicia L Degano, María A Contin
{"title":"Glial cell response to constant low light exposure in rat retina.","authors":"Manuel G Bruera,&nbsp;María M Benedetto,&nbsp;Mario E Guido,&nbsp;Alicia L Degano,&nbsp;María A Contin","doi":"10.1017/S0952523822000049","DOIUrl":null,"url":null,"abstract":"<p><p>To study the macroglia and microglia and the immune role in long-time light exposure in rat eyes, we performed glial cell characterization along the time-course of retinal degeneration induced by chronic exposure to low-intensity light. Animals were exposed to light for periods of 2, 4, 6, or 8 days, and the retinal glial response was evaluated by immunohistochemistry, western blot and real-time reverse transcription polymerase chain reaction. Retinal cells presented an increased expression of the macroglia marker GFAP, as well as increased mRNA levels of microglia markers Iba1 and CD68 after 6 days. Also, at this time-point, we found a higher number of Iba1-positive cells in the outer nuclear layer area; moreover, these cells showed the characteristic activated-microglia morphology. The expression levels of immune mediators TNF, IL-6, and chemokines CX3CR1 and CCL2 were also significantly increased after 6 days. All the events of glial activation occurred after 5-6 days of constant light exposure, when the number of photoreceptor cells has already decreased significantly. Herein, we demonstrated that glial and immune activation are secondary to neurodegeneration; in this scenario, our results suggest that photoreceptor death is an early event that occurs independently of glial-derived immune responses.</p>","PeriodicalId":23556,"journal":{"name":"Visual Neuroscience","volume":null,"pages":null},"PeriodicalIF":1.1000,"publicationDate":"2022-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Visual Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1017/S0952523822000049","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 4

Abstract

To study the macroglia and microglia and the immune role in long-time light exposure in rat eyes, we performed glial cell characterization along the time-course of retinal degeneration induced by chronic exposure to low-intensity light. Animals were exposed to light for periods of 2, 4, 6, or 8 days, and the retinal glial response was evaluated by immunohistochemistry, western blot and real-time reverse transcription polymerase chain reaction. Retinal cells presented an increased expression of the macroglia marker GFAP, as well as increased mRNA levels of microglia markers Iba1 and CD68 after 6 days. Also, at this time-point, we found a higher number of Iba1-positive cells in the outer nuclear layer area; moreover, these cells showed the characteristic activated-microglia morphology. The expression levels of immune mediators TNF, IL-6, and chemokines CX3CR1 and CCL2 were also significantly increased after 6 days. All the events of glial activation occurred after 5-6 days of constant light exposure, when the number of photoreceptor cells has already decreased significantly. Herein, we demonstrated that glial and immune activation are secondary to neurodegeneration; in this scenario, our results suggest that photoreceptor death is an early event that occurs independently of glial-derived immune responses.

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
大鼠视网膜神经胶质细胞对持续弱光照射的反应。
为了研究长时间光暴露对大鼠眼睛大胶质细胞和小胶质细胞的影响及其免疫作用,我们沿着慢性低强度光暴露引起的视网膜变性的时间过程对胶质细胞进行了表征。将动物暴露在光照下2、4、6或8天,通过免疫组织化学、western blot和实时逆转录聚合酶链反应来评估视网膜胶质细胞的反应。6天后,视网膜细胞大胶质细胞标记物GFAP表达增加,小胶质细胞标记物Iba1和CD68 mRNA水平升高。此外,在这个时间点,我们发现外核层区域有更多的iba1阳性细胞;此外,这些细胞表现出特有的激活小胶质细胞形态。免疫介质TNF、IL-6和趋化因子CX3CR1、CCL2的表达水平也在6天后显著升高。所有的神经胶质激活事件都发生在持续光照5-6天后,此时感光细胞数量已经明显减少。在这里,我们证明了神经胶质和免疫激活是继发于神经变性;在这种情况下,我们的结果表明,光感受器死亡是一个独立于神经胶质源性免疫反应发生的早期事件。
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
Visual Neuroscience
Visual Neuroscience 医学-神经科学
CiteScore
2.20
自引率
5.30%
发文量
8
审稿时长
>12 weeks
期刊介绍: Visual Neuroscience is an international journal devoted to the publication of experimental and theoretical research on biological mechanisms of vision. A major goal of publication is to bring together in one journal a broad range of studies that reflect the diversity and originality of all aspects of neuroscience research relating to the visual system. Contributions may address molecular, cellular or systems-level processes in either vertebrate or invertebrate species. The journal publishes work based on a wide range of technical approaches, including molecular genetics, anatomy, physiology, psychophysics and imaging, and utilizing comparative, developmental, theoretical or computational approaches to understand the biology of vision and visuo-motor control. The journal also publishes research seeking to understand disorders of the visual system and strategies for restoring vision. Studies based exclusively on clinical, psychophysiological or behavioral data are welcomed, provided that they address questions concerning neural mechanisms of vision or provide insight into visual dysfunction.
期刊最新文献
Synaptotagmin-9 in mouse retina Chemically induced cone degeneration in the 13-lined ground squirrel. Pre-stimulus bioelectrical activity in lightadapted ERG under blue versus white background - CORRIGENDUM. Evolution of the visual system in ray-finned fishes. Pre-stimulus bioelectrical activity in light-adapted ERG under blue versus white background
×
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