• 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

相似文献

1
ER stress and unfolded protein response in ocular health and disease.眼健康和疾病中的内质网应激和未折叠蛋白反应。
FEBS J. 2019 Jan;286(2):399-412. doi: 10.1111/febs.14522. Epub 2018 Jun 20.
2
Emerging roles of ER stress and unfolded protein response pathways in skeletal muscle health and disease.内质网应激和未折叠蛋白反应通路在骨骼肌健康与疾病中的新作用
J Cell Physiol. 2018 Jan;233(1):67-78. doi: 10.1002/jcp.25852. Epub 2017 May 16.
3
Cellular stress signaling and the unfolded protein response in retinal degeneration: mechanisms and therapeutic implications.细胞应激信号和未折叠蛋白反应在视网膜变性中的作用机制及治疗意义。
Mol Neurodegener. 2022 Mar 28;17(1):25. doi: 10.1186/s13024-022-00528-w.
4
The unfolded protein response in metazoan development.后生动物发育过程中的未折叠蛋白反应。
J Cell Sci. 2019 Feb 15;132(5):jcs217216. doi: 10.1242/jcs.217216.
5
Insights into the role of endoplasmic reticulum stress in skin function and associated diseases.内质网应激在皮肤功能和相关疾病中的作用的研究进展。
FEBS J. 2019 Jan;286(2):413-425. doi: 10.1111/febs.14739.
6
Liver function and dysfunction - a unique window into the physiological reach of ER stress and the unfolded protein response.肝功能障碍——内质网应激和未折叠蛋白反应的生理作用的独特窗口。
FEBS J. 2019 Jan;286(2):356-378. doi: 10.1111/febs.14389. Epub 2018 Feb 7.
7
The unfolded protein response and cellular senescence. A review in the theme: cellular mechanisms of endoplasmic reticulum stress signaling in health and disease.未折叠蛋白反应与细胞衰老。主题综述:健康与疾病中内质网应激信号的细胞机制
Am J Physiol Cell Physiol. 2015 Mar 15;308(6):C415-25. doi: 10.1152/ajpcell.00334.2014. Epub 2014 Dec 24.
8
The UPR: Sensor and Coordinator of Organismal Homeostasis.未折叠蛋白反应:机体稳态的传感器和协调器。
Mol Cell. 2017 Jun 15;66(6):761-771. doi: 10.1016/j.molcel.2017.05.031.
9
Adenoviral CCN gene transfers induce in vitro and in vivo endoplasmic reticulum stress and unfolded protein response.腺病毒CCN基因转导可在体外和体内诱导内质网应激及未折叠蛋白反应。
Biochim Biophys Acta. 2016 Nov;1863(11):2604-2612. doi: 10.1016/j.bbamcr.2016.07.006. Epub 2016 Jul 22.
10
TULP1 Missense Mutations Induces the Endoplasmic Reticulum Unfolded Protein Response Stress Complex (ER-UPR).TULP1错义突变诱导内质网未折叠蛋白反应应激复合体(ER-UPR)。
Adv Exp Med Biol. 2016;854:223-30. doi: 10.1007/978-3-319-17121-0_30.

引用本文的文献

1
Molecular Underpinning of Treatment-Resistant Schizophrenia: A Putative Different Neurobiology from Treatment-Responsive Schizophrenia.难治性精神分裂症的分子基础:与反应性精神分裂症不同的假定神经生物学机制
Int J Mol Sci. 2025 Sep 4;26(17):8598. doi: 10.3390/ijms26178598.
2
Functionally deficient UBOX5 variants and primary angle-closure glaucoma.功能缺陷型UBOX5变体与原发性闭角型青光眼
Nat Commun. 2025 Aug 15;16(1):7620. doi: 10.1038/s41467-025-62775-x.
3
Diabetic retinopathy and Alzheimer's disease: Convergence of the unfolded protein response in neurodegeneration.糖尿病视网膜病变与阿尔茨海默病:神经退行性变中未折叠蛋白反应的交汇
Alzheimers Dement. 2025 Aug;21(8):e70497. doi: 10.1002/alz.70497.
4
Bidirectional Phosphorylation Changes in Opsins Associated With Early Myopia and Hyperopia Signal Regulation by Phosphoproteomics.通过磷酸化蛋白质组学研究视蛋白的双向磷酸化变化与早期近视和远视信号调节的关系
Invest Ophthalmol Vis Sci. 2025 Jul 1;66(9):70. doi: 10.1167/iovs.66.9.70.
5
Retinoid X receptor agonist 9CDHRA mitigates retinal ganglion cell apoptosis and neuroinflammation in a mouse model of glaucoma.维甲酸X受体激动剂9CDHRA减轻青光眼小鼠模型中的视网膜神经节细胞凋亡和神经炎症。
FASEB J. 2025 Mar 31;39(6):e70465. doi: 10.1096/fj.202402642R.
6
C/EBP Homologous Protein Expression in Retinal Ganglion Cells Induces Neurodegeneration in Mice.视网膜神经节细胞中C/EBP同源蛋白的表达诱导小鼠神经退行性变。
Int J Mol Sci. 2025 Feb 21;26(5):1858. doi: 10.3390/ijms26051858.
7
Influences of lead-based perovskite nanoparticles exposure on early development of human retina.基于铅的钙钛矿纳米颗粒暴露对人类视网膜早期发育的影响。
J Nanobiotechnology. 2025 Feb 26;23(1):144. doi: 10.1186/s12951-025-03245-w.
8
Acid-sensing ion channel 1a promotes alcohol-associated liver disease in mice via regulating endoplasmic reticulum autophagy.酸敏感离子通道1a通过调节内质网自噬促进小鼠酒精性肝病。
Acta Pharmacol Sin. 2025 Apr;46(4):989-1001. doi: 10.1038/s41401-024-01423-4. Epub 2024 Nov 26.
9
Homeostasis control in health and disease by the unfolded protein response.未折叠蛋白反应对健康和疾病中的体内平衡控制
Nat Rev Mol Cell Biol. 2025 Mar;26(3):193-212. doi: 10.1038/s41580-024-00794-0. Epub 2024 Nov 5.
10
Eucalyptol Ameliorates Retinal Microvascular Defects through Modulating ER Stress and Angiopoietin-Tie Signaling in Diabetic Eyes.桉油醇通过调节糖尿病眼中的内质网应激和血管生成素-Tie 信号改善视网膜微血管病变。
Int J Mol Sci. 2024 Jul 17;25(14):7826. doi: 10.3390/ijms25147826.

本文引用的文献

1
The unfolded protein response regulator ATF6 promotes mesodermal differentiation.未折叠蛋白反应调节因子 ATF6 促进中胚层分化。
Sci Signal. 2018 Feb 13;11(517):eaan5785. doi: 10.1126/scisignal.aan5785.
2
Autosomal recessive cone-rod dystrophy can be caused by mutations in the ATF6 gene.常染色体隐性遗传性锥杆营养不良可由ATF6基因突变引起。
Eur J Hum Genet. 2017 Nov;25(11):1210-1216. doi: 10.1038/ejhg.2017.131. Epub 2017 Aug 16.
3
Achromatopsia mutations target sequential steps of ATF6 activation.色盲突变针对激活转录激活因子6(ATF6)的连续步骤。
Proc Natl Acad Sci U S A. 2017 Jan 10;114(2):400-405. doi: 10.1073/pnas.1606387114. Epub 2016 Dec 27.
4
Senescence-associated secretory phenotype contributes to pathological angiogenesis in retinopathy.衰老相关 secretory phenotype 促进视网膜病变中的病理性血管生成。
Sci Transl Med. 2016 Oct 26;8(362):362ra144. doi: 10.1126/scitranslmed.aaf9440.
5
Pathogenic mutations in TULP1 responsible for retinitis pigmentosa identified in consanguineous familial cases.在近亲家族性病例中发现导致色素性视网膜炎的TULP1致病突变。
Mol Vis. 2016 Jul 16;22:797-815. eCollection 2016.
6
Limited ATF4 Expression in Degenerating Retinas with Ongoing ER Stress Promotes Photoreceptor Survival in a Mouse Model of Autosomal Dominant Retinitis Pigmentosa.在伴有持续性内质网应激的退化视网膜中,有限的活化转录因子4(ATF4)表达可促进常染色体显性视网膜色素变性小鼠模型中的光感受器存活。
PLoS One. 2016 May 4;11(5):e0154779. doi: 10.1371/journal.pone.0154779. eCollection 2016.
7
Endoplasmic reticulum stress in human photoreceptor diseases.人类光感受器疾病中的内质网应激
Brain Res. 2016 Oct 1;1648(Pt B):538-541. doi: 10.1016/j.brainres.2016.04.021. Epub 2016 Apr 23.
8
Involvement of Endoplasmic Reticulum Stress in TULP1 Induced Retinal Degeneration.内质网应激在TULP1诱导的视网膜变性中的作用
PLoS One. 2016 Mar 17;11(3):e0151806. doi: 10.1371/journal.pone.0151806. eCollection 2016.
9
Naturally occurring p16(Ink4a)-positive cells shorten healthy lifespan.天然存在的p16(Ink4a)阳性细胞会缩短健康寿命。
Nature. 2016 Feb 11;530(7589):184-9. doi: 10.1038/nature16932. Epub 2016 Feb 3.
10
Cellular senescence in aging and age-related disease: from mechanisms to therapy.衰老及衰老相关疾病中的细胞衰老:从机制到治疗
Nat Med. 2015 Dec;21(12):1424-35. doi: 10.1038/nm.4000.

眼健康和疾病中的内质网应激和未折叠蛋白反应。

ER stress and unfolded protein response in ocular health and disease.

机构信息

Department of Pathology, University of California San Diego, La Jolla, CA, USA.

Institute for Ophthalmic Research, Centre for Ophthalmology, University of Tübingen, Germany.

出版信息

FEBS J. 2019 Jan;286(2):399-412. doi: 10.1111/febs.14522. Epub 2018 Jun 20.

DOI:10.1111/febs.14522
PMID:29802807
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6583901/
Abstract

The human eye is the organ that is able to react to light in order to provide sharp three-dimensional and colored images. Unfortunately, the health of the eye can be impacted by various stimuli that can lead to vision loss, such as environmental changes, genetic mutations, or aging. Endoplasmic reticulum (ER) stress and unfolded protein response (UPR) signaling have been detected in many diverse ocular diseases, and chemical and genetic approaches to modulate ER stress and specific UPR regulatory molecules have shown beneficial effects in animal models of eye disease. This review highlights specific eye diseases associated with ER stress and UPR activity, based on a recent symposia exploring this theme.

摘要

人眼是能够对光做出反应以提供清晰的三维和彩色图像的器官。不幸的是,眼睛的健康可能会受到各种刺激的影响,导致视力丧失,如环境变化、基因突变或衰老。内质网(ER)应激和未折叠蛋白反应(UPR)信号已在许多不同的眼部疾病中被检测到,并且化学和遗传方法来调节 ER 应激和特定的 UPR 调节分子在眼部疾病的动物模型中显示出了有益的效果。这篇综述根据最近探讨这一主题的专题研讨会,突出了与 ER 应激和 UPR 活性相关的特定眼部疾病。