• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

过氧化物酶体增殖物激活受体γ与脑部病毒感染

PPAR Gamma and Viral Infections of the Brain.

机构信息

Toulouse NeuroImaging Center (ToNIC), INSERM/UPS UMR 1214, CHU Toulouse-Purpan, 31024 Toulouse, France.

出版信息

Int J Mol Sci. 2021 Aug 18;22(16):8876. doi: 10.3390/ijms22168876.

DOI:10.3390/ijms22168876
PMID:34445581
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8396218/
Abstract

Peroxisome Proliferator-Activated Receptor gamma (PPARγ) is a master regulator of metabolism, adipogenesis, inflammation and cell cycle, and it has been extensively studied in the brain in relation to inflammation or neurodegeneration. Little is known however about its role in viral infections of the brain parenchyma, although they represent the most frequent cause of encephalitis and are a major threat for the developing brain. Specific to viral infections is the ability to subvert signaling pathways of the host cell to ensure virus replication and spreading, as deleterious as the consequences may be for the host. In this respect, the pleiotropic role of PPARγ makes it a critical target of infection. This review aims to provide an update on the role of PPARγ in viral infections of the brain. Recent studies have highlighted the involvement of PPARγ in brain or neural cells infected by immunodeficiency virus 1, Zika virus, or human cytomegalovirus. They have provided a better understanding on PPARγ functions in the infected brain, and revealed that it can be a double-edged sword with respect to inflammation, viral replication, or neuronogenesis. They unraveled new roles of PPARγ in health and disease and could possibly help designing new therapeutic strategies.

摘要

过氧化物酶体增殖物激活受体 γ(PPARγ)是代谢、脂肪生成、炎症和细胞周期的主要调节剂,它在与炎症或神经退行性变有关的大脑中得到了广泛研究。然而,关于其在脑实质病毒感染中的作用,人们知之甚少,尽管它们是脑炎最常见的原因,也是发育中大脑的主要威胁。特定于病毒感染的是能够颠覆宿主细胞的信号通路,以确保病毒复制和传播的能力,尽管这对宿主可能产生有害的后果。在这方面,PPARγ 的多效性作用使其成为感染的关键靶点。本综述旨在提供有关 PPARγ 在脑病毒感染中的作用的最新信息。最近的研究强调了 PPARγ 在感染免疫缺陷病毒 1、寨卡病毒或人类巨细胞病毒的脑或神经细胞中的作用。它们提供了对感染大脑中 PPARγ 功能的更好理解,并表明它在炎症、病毒复制或神经元发生方面可能是一把双刃剑。它们揭示了 PPARγ 在健康和疾病中的新作用,并可能有助于设计新的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/152b/8396218/758e7adf9f74/ijms-22-08876-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/152b/8396218/35a83538402d/ijms-22-08876-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/152b/8396218/fd6ef04f705b/ijms-22-08876-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/152b/8396218/758e7adf9f74/ijms-22-08876-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/152b/8396218/35a83538402d/ijms-22-08876-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/152b/8396218/fd6ef04f705b/ijms-22-08876-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/152b/8396218/758e7adf9f74/ijms-22-08876-g003.jpg

相似文献

1
PPAR Gamma and Viral Infections of the Brain.过氧化物酶体增殖物激活受体γ与脑部病毒感染
Int J Mol Sci. 2021 Aug 18;22(16):8876. doi: 10.3390/ijms22168876.
2
PPARγ Is Activated during Congenital Cytomegalovirus Infection and Inhibits Neuronogenesis from Human Neural Stem Cells.过氧化物酶体增殖物激活受体γ在先天性巨细胞病毒感染过程中被激活,并抑制人类神经干细胞的神经发生。
PLoS Pathog. 2016 Apr 14;12(4):e1005547. doi: 10.1371/journal.ppat.1005547. eCollection 2016 Apr.
3
Peroxisome proliferator-activated receptor-gamma: potential molecular therapeutic target for HIV-1-associated brain inflammation.过氧化物酶体增殖物激活受体-γ:HIV-1 相关脑炎症的潜在分子治疗靶点。
J Neuroinflammation. 2017 Sep 8;14(1):183. doi: 10.1186/s12974-017-0957-8.
4
Hippo Signaling Pathway Has a Critical Role in Zika Virus Replication and in the Pathogenesis of Neuroinflammation.Hippo 信号通路在寨卡病毒复制和神经炎症发病机制中具有关键作用。
Am J Pathol. 2020 Apr;190(4):844-861. doi: 10.1016/j.ajpath.2019.12.005. Epub 2020 Feb 5.
5
Zika Virus Subgenomic Flavivirus RNA Generation Requires Cooperativity between Duplicated RNA Structures That Are Essential for Productive Infection in Human Cells.寨卡病毒亚基因组黄病毒 RNA 的生成需要重复 RNA 结构之间的协作,这些结构对于在人细胞中进行有效感染是必不可少的。
J Virol. 2020 Aug 31;94(18). doi: 10.1128/JVI.00343-20.
6
Genetic Diversity of Collaborative Cross Mice Controls Viral Replication, Clinical Severity, and Brain Pathology Induced by Zika Virus Infection, Independently of .协同杂交小鼠的遗传多样性可独立于控制寨卡病毒感染引起的病毒复制、临床严重程度和脑组织病理学
J Virol. 2020 Jan 17;94(3). doi: 10.1128/JVI.01034-19.
7
Peroxisome Proliferator-Activated Receptor Gamma (PPARγ) as a Target for Concurrent Management of Diabetes and Obesity-Related Cancer.过氧化物酶体增殖物激活受体 γ(PPARγ)作为同时管理糖尿病和肥胖相关癌症的靶点。
Curr Pharm Des. 2017;23(25):3677-3688. doi: 10.2174/1381612823666170704125104.
8
Zika Virus Infection Induces DNA Damage Response in Human Neural Progenitors That Enhances Viral Replication.寨卡病毒感染诱导人神经祖细胞中的 DNA 损伤反应,从而增强病毒复制。
J Virol. 2019 Sep 30;93(20). doi: 10.1128/JVI.00638-19. Print 2019 Oct 15.
9
Neuronal seipin knockout facilitates Aβ-induced neuroinflammation and neurotoxicity via reduction of PPARγ in hippocampus of mouse.神经元丝氨酸棕榈酰转移酶缺失通过降低小鼠海马体中过氧化物酶体增殖物激活受体γ(PPARγ)的水平,促进β淀粉样蛋白(Aβ)诱导的神经炎症和神经毒性。
J Neuroinflammation. 2016 Jun 10;13(1):145. doi: 10.1186/s12974-016-0598-3.
10
Peroxisome proliferator-activated receptor-γ cofactors in neurodegeneration.过氧化物酶体增殖物激活受体-γ 共激活因子与神经退行性变。
IUBMB Life. 2012 Dec;64(12):958-64. doi: 10.1002/iub.1097. Epub 2012 Nov 6.

引用本文的文献

1
Congenital Heart Diseases and Neurodevelopmental Disorders: New Insights Through the DOHaD Hypothesis.先天性心脏病与神经发育障碍:通过发育起源健康与疾病假说获得的新见解
JACC Basic Transl Sci. 2025 Aug;10(8):101251. doi: 10.1016/j.jacbts.2025.01.022. Epub 2025 Apr 23.
2
Host centric drug repurposing for viral diseases.以宿主为中心的病毒疾病药物再利用
PLoS Comput Biol. 2025 Apr 2;21(4):e1012876. doi: 10.1371/journal.pcbi.1012876. eCollection 2025 Apr.
3
Cytomegalovirus infection of the fetal brain: intake of aspirin during pregnancy blunts neurodevelopmental pathogenesis in the offspring.

本文引用的文献

1
Comprehensive Review on Neuro-COVID-19 Pathophysiology and Clinical Consequences.神经新冠病毒病的病理生理学和临床后果的综合综述。
Neurotox Res. 2021 Oct;39(5):1613-1629. doi: 10.1007/s12640-021-00389-z. Epub 2021 Jun 25.
2
PPARgamma in Metabolism, Immunity, and Cancer: Unified and Diverse Mechanisms of Action.PPARγ 在代谢、免疫和癌症中的作用:统一和多样化的作用机制。
Front Endocrinol (Lausanne). 2021 Feb 26;12:624112. doi: 10.3389/fendo.2021.624112. eCollection 2021.
3
Human cytomegalovirus infection is associated with increased expression of the lissencephaly gene PAFAH1B1 encoding LIS1 in neural stem cells and congenitally infected brains.
巨细胞病毒感染胎儿大脑:怀孕期间服用阿司匹林可削弱后代的神经发育发病机制。
J Neuroinflammation. 2024 Nov 15;21(1):298. doi: 10.1186/s12974-024-03276-4.
4
Cellular metabolism hijacked by viruses for immunoevasion: potential antiviral targets.病毒劫持细胞代谢以实现免疫逃避:潜在的抗病毒靶点。
Front Immunol. 2023 Jul 25;14:1228811. doi: 10.3389/fimmu.2023.1228811. eCollection 2023.
5
Astrocytes derived from neural progenitor cells are susceptible to Zika virus infection.神经祖细胞衍生的星形胶质细胞易感染寨卡病毒。
PLoS One. 2023 Mar 29;18(3):e0283429. doi: 10.1371/journal.pone.0283429. eCollection 2023.
6
Peroxisome Proliferator-Activated Receptor-Targeted Therapies: Challenges upon Infectious Diseases.过氧化物酶体增殖物激活受体靶向治疗:感染性疾病面临的挑战。
Cells. 2023 Feb 17;12(4):650. doi: 10.3390/cells12040650.
7
Update on Anti-Inflammatory Molecular Mechanisms Induced by Oleic Acid.油酸诱导抗炎分子机制的最新研究进展。
Nutrients. 2023 Jan 1;15(1):224. doi: 10.3390/nu15010224.
8
Fetal Brain Damage in Human Fetuses with Congenital Cytomegalovirus Infection: Histological Features and Viral Tropism.先天性巨细胞病毒感染胎儿的脑损伤:组织学特征和病毒嗜性。
Cell Mol Neurobiol. 2023 Apr;43(3):1385-1399. doi: 10.1007/s10571-022-01258-9. Epub 2022 Aug 7.
9
PPARs as Key Mediators in the Regulation of Metabolism and Inflammation.过氧化物酶体增殖物激活受体(PPARs)作为调节代谢和炎症的关键介质。
Int J Mol Sci. 2022 Apr 30;23(9):5025. doi: 10.3390/ijms23095025.
10
Polarization of Microglia and Its Therapeutic Potential in Sepsis.小胶质细胞极化及其在脓毒症中的治疗潜力。
Int J Mol Sci. 2022 Apr 28;23(9):4925. doi: 10.3390/ijms23094925.
人类巨细胞病毒感染与神经干细胞和先天性感染大脑中 Lissencephaly 基因 PAFAH1B1 编码的 LIS1 表达增加有关。
J Pathol. 2021 May;254(1):92-102. doi: 10.1002/path.5640. Epub 2021 Mar 24.
4
Comparison of PPAR Ligands as Modulators of Resolution of Inflammation, via Their Influence on Cytokines and Oxylipins Release in Astrocytes.比较过氧化物酶体增殖物激活受体配体作为炎症消退的调节剂,通过它们对星形胶质细胞细胞因子和氧化脂类释放的影响。
Int J Mol Sci. 2020 Dec 16;21(24):9577. doi: 10.3390/ijms21249577.
5
Rice Bran Extract Protected against LPS-Induced Neuroinflammation in Mice through Targeting PPAR-γ Nuclear Receptor.米糠提取物通过靶向 PPAR-γ 核受体保护 LPS 诱导的小鼠神经炎症。
Mol Neurobiol. 2021 Apr;58(4):1504-1516. doi: 10.1007/s12035-020-02196-7. Epub 2020 Nov 18.
6
The Presence of Human Herpesvirus 6 in the Brain in Health and Disease.人类疱疹病毒 6 在健康和疾病中的大脑存在。
Biomolecules. 2020 Nov 6;10(11):1520. doi: 10.3390/biom10111520.
7
Two Rationally Identified Novel Glitazones Reversed the Behavioral Dysfunctions and Exhibited Neuroprotection Through Ameliorating Brain Cytokines and Oxy-Radicals in ICV-LPS Neuroinflammatory Rat Model.两种经合理鉴定的新型格列酮类药物在脑室内注射脂多糖神经炎症大鼠模型中,通过改善脑内细胞因子和氧自由基,逆转了行为功能障碍并表现出神经保护作用。
Front Neurosci. 2020 Sep 25;14:530148. doi: 10.3389/fnins.2020.530148. eCollection 2020.
8
NRF2 and PPAR-γ Pathways in Oligodendrocyte Progenitors: Focus on ROS Protection, Mitochondrial Biogenesis and Promotion of Cell Differentiation.NRF2 和 PPAR-γ 通路在少突胶质前体细胞中的作用:重点关注 ROS 保护、线粒体生物发生和促进细胞分化。
Int J Mol Sci. 2020 Sep 29;21(19):7216. doi: 10.3390/ijms21197216.
9
Propofol ameliorates neuropathic pain and neuroinflammation through PPAR γ up-regulation to block Wnt/β-catenin pathway.丙泊酚通过上调 PPARγ 抑制 Wnt/β-连环蛋白通路来改善神经病理性疼痛和神经炎症。
Neurol Res. 2021 Jan;43(1):71-77. doi: 10.1080/01616412.2020.1823107. Epub 2020 Sep 27.
10
Regulation of Proinflammatory Enzymes by Peroxisome Proliferator-Activated Receptor Gamma in Astroglia Infected with Toxoplasma gondii.过氧化物酶体增殖物激活受体γ调控弓形虫感染星形胶质细胞中促炎酶的表达。
J Parasitol. 2020 Oct 1;106(5):564-571. doi: 10.1645/18-184.