Microglial depletion decreases Müller cell maturation and inner retinal vascular density.

IF 8.2 2区 生物学 Q1 CELL BIOLOGY Cell Communication and Signaling Pub Date : 2025-02-17 DOI:10.1186/s12964-025-02083-5
Nathaniel Rowthorn-Apel, Naveen Vridhachalam, Kip M Connor, Gracia M Bonilla, Ruslan Sadreyev, Charandeep Singh, Gopalan Gnanaguru
{"title":"Microglial depletion decreases Müller cell maturation and inner retinal vascular density.","authors":"Nathaniel Rowthorn-Apel, Naveen Vridhachalam, Kip M Connor, Gracia M Bonilla, Ruslan Sadreyev, Charandeep Singh, Gopalan Gnanaguru","doi":"10.1186/s12964-025-02083-5","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The neuroretinal vascular system is comprised of three interconnected layers. The initial superficial vascular plexus formation is guided by astrocytes around birth in mice. The formation of the deep and intermediate vascular plexuses occurs in the second postnatal week and is driven by Müller-cell-derived angiogenic signaling. Previously, we reported that microglia play an important role in regulating astrocyte density during superficial vascular plexus formation. Here, we investigated the role of microglia in regulating Müller-cell-dependent inner retinal vascular development.</p><p><strong>Methodology: </strong>In this study, we depleted microglia during retinal development using Csf1R antagonist (PLX5622). We characterized the developmental progression of inner retinal vascular growth, effect of microglial depletion on inner retinal vascular growth and Müller cell marker expressions by immunostaining. Differential expressions of genes in the control and microglia depleted groups were analyzed by mRNA-seq and qPCR. Unpaired t-test was performed to determine the statistical differences between groups.</p><p><strong>Results: </strong>This study show that microglia interact with Müller cells and the growing inner retinal vasculature. Depletion of microglia resulted in reduced inner retinal vascular layers densities and decreased Vegfa isoforms transcript levels. RNA-seq analysis further revealed that microglial depletion significantly reduced specific Müller cell maturation markers including glutamine synthetase, responsible for glutamine biosynthesis, necessary for angiogenesis.</p><p><strong>Conclusions: </strong>Our study reveals an important role for microglia in facilitating inner retinal angiogenesis and Müller cell maturation.</p>","PeriodicalId":55268,"journal":{"name":"Cell Communication and Signaling","volume":"23 1","pages":"90"},"PeriodicalIF":8.2000,"publicationDate":"2025-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11831819/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell Communication and Signaling","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s12964-025-02083-5","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: The neuroretinal vascular system is comprised of three interconnected layers. The initial superficial vascular plexus formation is guided by astrocytes around birth in mice. The formation of the deep and intermediate vascular plexuses occurs in the second postnatal week and is driven by Müller-cell-derived angiogenic signaling. Previously, we reported that microglia play an important role in regulating astrocyte density during superficial vascular plexus formation. Here, we investigated the role of microglia in regulating Müller-cell-dependent inner retinal vascular development.

Methodology: In this study, we depleted microglia during retinal development using Csf1R antagonist (PLX5622). We characterized the developmental progression of inner retinal vascular growth, effect of microglial depletion on inner retinal vascular growth and Müller cell marker expressions by immunostaining. Differential expressions of genes in the control and microglia depleted groups were analyzed by mRNA-seq and qPCR. Unpaired t-test was performed to determine the statistical differences between groups.

Results: This study show that microglia interact with Müller cells and the growing inner retinal vasculature. Depletion of microglia resulted in reduced inner retinal vascular layers densities and decreased Vegfa isoforms transcript levels. RNA-seq analysis further revealed that microglial depletion significantly reduced specific Müller cell maturation markers including glutamine synthetase, responsible for glutamine biosynthesis, necessary for angiogenesis.

Conclusions: Our study reveals an important role for microglia in facilitating inner retinal angiogenesis and Müller cell maturation.

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
小胶质细胞耗竭会降低 Müller 细胞成熟度和视网膜内层血管密度。
背景:神经视网膜血管系统由三个相互连接的层组成。小鼠出生前后星形胶质细胞引导初始浅表血管丛形成。深血管丛和中间血管丛的形成发生在出生后的第二周,并由勒细胞来源的血管生成信号驱动。以前,我们报道了小胶质细胞在浅表血管丛形成过程中对星形胶质细胞密度的调节起重要作用。在这里,我们研究了小胶质细胞在调节勒细胞依赖性视网膜内血管发育中的作用。方法:在这项研究中,我们使用Csf1R拮抗剂(PLX5622)在视网膜发育过程中去除小胶质细胞。我们用免疫染色法观察了视网膜内血管生长的发育过程、小胶质细胞缺失对视网膜内血管生长的影响和 ller细胞标记物的表达。通过mRNA-seq和qPCR分析对照组和小胶质细胞缺失组基因的差异表达。采用非配对t检验确定组间的统计学差异。结果:本研究表明,小胶质细胞与m ller细胞和正在生长的视网膜内血管相互作用。小胶质细胞的缺失导致视网膜内血管层密度降低,Vegfa同种异构体转录水平降低。RNA-seq分析进一步显示,小胶质细胞缺失显著降低了特定的细胞成熟标志物,包括谷氨酰胺合成酶,谷氨酰胺合成酶负责谷氨酰胺的生物合成,是血管生成所必需的。结论:我们的研究揭示了小胶质细胞在促进视网膜内血管生成和 ller细胞成熟中的重要作用。
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
CiteScore
11.00
自引率
0.00%
发文量
180
期刊介绍: Cell Communication and Signaling (CCS) is a peer-reviewed, open-access scientific journal that focuses on cellular signaling pathways in both normal and pathological conditions. It publishes original research, reviews, and commentaries, welcoming studies that utilize molecular, morphological, biochemical, structural, and cell biology approaches. CCS also encourages interdisciplinary work and innovative models, including in silico, in vitro, and in vivo approaches, to facilitate investigations of cell signaling pathways, networks, and behavior. Starting from January 2019, CCS is proud to announce its affiliation with the International Cell Death Society. The journal now encourages submissions covering all aspects of cell death, including apoptotic and non-apoptotic mechanisms, cell death in model systems, autophagy, clearance of dying cells, and the immunological and pathological consequences of dying cells in the tissue microenvironment.
期刊最新文献
CD80+ Macrophage-Induced IL-17+CD8+ T cells accumulate in hyperlipidemic patients and murine vascular lesions to promote atherosclerotic progression. Ribosome transfer via tunnelling nanotubes rescues protein synthesis in pancreatic cancer cells. ADAM17, induced by Augmenter of Liver Regeneration via G protein-coupled receptor activation, transactivates epidermal growth factor-receptor and reduces classical IL-6 signaling. Deficiency of interleukin-40 prevents intestinal damage in experimental necrotizing enterocolitis by inhibiting NETosis. Mitochondrial preservation through the PKA-DRP1 axis empowers natural killer cells to resist acidic stress and retain cytotoxicity.
×
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:604180095
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