• 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

TNIP1 在调节受体后信号转导中的新兴作用。

Emerging roles for TNIP1 in regulating post-receptor signaling.

机构信息

Graduate Program in Pharmacology & Toxicology, University of Connecticut, Storrs, CT 06269-3092, USA.

出版信息

Cytokine Growth Factor Rev. 2012 Jun;23(3):109-18. doi: 10.1016/j.cytogfr.2012.04.002. Epub 2012 Apr 28.

DOI:10.1016/j.cytogfr.2012.04.002
PMID:22542476
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3366012/
Abstract

A vast number of cellular processes and signaling pathways are regulated by various receptors, ranging from transmembrane to nuclear receptors. These receptor-mediated processes are modulated by a diverse set of regulatory proteins. TNFα-induced protein 3-interacting protein 1 is such a protein that inhibits both transduction by transmembrane receptors, such as TNFα-receptor, EGF-R, and TLR, and nuclear receptors' PPAR and RAR activity. These receptors play key roles in regulating inflammation and inflammatory diseases. A growing number of references have implicated TNIP1 through GWAS and expression studies in chronic inflammatory diseases such as psoriasis and rheumatoid arthritis, although TNIP1s exact role has yet been determined. In this review, we aim to integrate the current knowledge of TNIP1s functions with the diseases in which it has been associated to potentially elucidate the role this regulator has in promoting or alleviating these inflammatory diseases.

摘要

大量的细胞过程和信号通路受到各种受体的调节,这些受体从跨膜受体到核受体都有。这些受体介导的过程受到多种调节蛋白的调节。TNFα 诱导蛋白 3 相互作用蛋白 1 就是这样一种蛋白,它抑制了跨膜受体(如 TNFα 受体、EGF-R 和 TLR)和核受体的 PPAR 和 RAR 活性的转导。这些受体在调节炎症和炎症性疾病中起着关键作用。越来越多的参考文献通过 GWAS 和表达研究将 TNIP1 与慢性炎症性疾病(如银屑病和类风湿关节炎)联系起来,尽管 TNIP1 的确切作用尚未确定。在这篇综述中,我们旨在整合 TNIP1 功能的现有知识及其与疾病的关联,以潜在阐明该调节剂在促进或缓解这些炎症性疾病中的作用。

相似文献

1
Emerging roles for TNIP1 in regulating post-receptor signaling.TNIP1 在调节受体后信号转导中的新兴作用。
Cytokine Growth Factor Rev. 2012 Jun;23(3):109-18. doi: 10.1016/j.cytogfr.2012.04.002. Epub 2012 Apr 28.
2
TNIP1 in Autoimmune Diseases: Regulation of Toll-like Receptor Signaling.TNIP1 在自身免疫性疾病中的作用:调节 Toll 样受体信号转导。
J Immunol Res. 2018 Oct 3;2018:3491269. doi: 10.1155/2018/3491269. eCollection 2018.
3
Downregulation of TNIP1 Expression Leads to Increased Proliferation of Human Keratinocytes and Severer Psoriasis-Like Conditions in an Imiquimod-Induced Mouse Model of Dermatitis.在咪喹莫特诱导的小鼠皮炎模型中,TNIP1表达下调导致人角质形成细胞增殖增加和更严重的银屑病样症状。
PLoS One. 2015 Jun 5;10(6):e0127957. doi: 10.1371/journal.pone.0127957. eCollection 2015.
4
TNIP1 reduction sensitizes keratinocytes to post-receptor signalling following exposure to TLR agonists.TNIP1 的减少使角质形成细胞在接触 TLR 激动剂后对受体后信号敏感。
Cell Signal. 2018 May;45:81-92. doi: 10.1016/j.cellsig.2018.02.004. Epub 2018 Feb 5.
5
Ligands of peroxisome proliferator-activated receptor-gamma induce apoptosis in AR42J cells.过氧化物酶体增殖物激活受体γ的配体诱导AR42J细胞凋亡。
Pancreas. 2002 Mar;24(2):130-8. doi: 10.1097/00006676-200203000-00003.
6
TNIP1 reduction of HSPA6 gene expression occurs in promoter regions lacking binding sites for known TNIP1-repressed transcription factors.HSPA6基因表达的TNIP1降低发生在缺乏已知TNIP1抑制转录因子结合位点的启动子区域。
Gene. 2015 Jan 25;555(2):430-7. doi: 10.1016/j.gene.2014.11.012. Epub 2014 Nov 12.
7
The role of lipid-activated nuclear receptors in shaping macrophage and dendritic cell function: From physiology to pathology.脂质激活的核受体在塑造巨噬细胞和树突状细胞功能中的作用:从生理学到病理学。
J Allergy Clin Immunol. 2013 Aug;132(2):264-86. doi: 10.1016/j.jaci.2013.05.044.
8
Cross-talk between janus kinase-signal transducer and activator of transcription (JAK-STAT) and peroxisome proliferator-activated receptor-alpha (PPARalpha) signaling pathways. Growth hormone inhibition of pparalpha transcriptional activity mediated by stat5b.Janus激酶-信号转导子和转录激活子(JAK-STAT)与过氧化物酶体增殖物激活受体α(PPARα)信号通路之间的相互作用。生长激素对由Stat5b介导的PPARα转录活性的抑制作用。
J Biol Chem. 1999 Jan 29;274(5):2672-81. doi: 10.1074/jbc.274.5.2672.
9
Enhanced Wound Healing- and Inflammasome-Associated Gene Expression in TNFAIP3-Interacting Protein 1- (TNIP1-) Deficient HaCaT Keratinocytes Parallels Reduced Reepithelialization.TNFAIP3 相互作用蛋白 1(TNIP1)缺陷的 HaCaT 角质形成细胞中增强的伤口愈合和炎症小体相关基因表达与减少的再上皮化平行。
Mediators Inflamm. 2020 Apr 21;2020:5919150. doi: 10.1155/2020/5919150. eCollection 2020.
10
Combinatorial roles of nuclear receptors in inflammation and immunity.核受体在炎症和免疫中的组合作用。
Nat Rev Immunol. 2006 Jan;6(1):44-55. doi: 10.1038/nri1748.

引用本文的文献

1
Multiomic Evidence for a Unified Model of Alzheimer's Disease Etiology Linking Microglial Flux Capacity and Astrocyte-Neuron Metabolic Breakdown.阿尔茨海默病病因统一模型的多组学证据:连接小胶质细胞通量能力与星形胶质细胞-神经元代谢分解
bioRxiv. 2025 May 12:2024.07.23.604835. doi: 10.1101/2024.07.23.604835.
2
HIV-1 Nef activates proviral DNA transcription by recruiting Src kinase to phosphorylate host protein Nef-associated factor 1 to compromise its viral restrictive function.HIV-1 Nef通过招募Src激酶磷酸化宿主蛋白Nef相关因子1来激活前病毒DNA转录,从而损害其病毒限制功能。
J Virol. 2025 May 20;99(5):e0028025. doi: 10.1128/jvi.00280-25. Epub 2025 Apr 24.
3

本文引用的文献

1
Genome-wide meta-analysis of psoriatic arthritis identifies susceptibility locus at REL.全基因组荟萃分析发现 REL 是银屑病关节炎的易感基因位点。
J Invest Dermatol. 2012 Apr;132(4):1133-40. doi: 10.1038/jid.2011.415. Epub 2011 Dec 15.
2
TNIP1, a retinoic acid receptor corepressor and A20-binding inhibitor of NF-κB, distributes to both nuclear and cytoplasmic locations.TNIP1,一种维甲酸受体核心抑制物和 NF-κB 的 A20 结合抑制剂,分布于核和细胞质位置。
J Histochem Cytochem. 2011 Dec;59(12):1101-12. doi: 10.1369/0022155411427728.
3
A pro-inflammatory role for A20 and ABIN family proteins in human fibroblast-like synoviocytes in rheumatoid arthritis.
Conformational Analyses of the AHD1-UBAN Region of TNIP1 Highlight Key Amino Acids for Interaction with Ubiquitin.
TNIP1的AHD1-UBAN区域的构象分析突出了与泛素相互作用的关键氨基酸。
Biomolecules. 2025 Mar 20;15(3):453. doi: 10.3390/biom15030453.
4
Host factor Naf1 restricts HIV-1 infection of myeloid cells and compromises the capacity of dendritic cell to prime CD4 T cell.宿主因子Naf1限制HIV-1对髓系细胞的感染,并损害树突状细胞激活CD4 T细胞的能力。
Virol Sin. 2025 Apr;40(2):217-224. doi: 10.1016/j.virs.2025.03.007. Epub 2025 Mar 24.
5
LncRNA-Gm17586 inhibits S.typhimurium mediated pyroptosis by promoting NLRP3 and Tnip1 binding.长链非编码RNA-Gm17586通过促进NLRP3与Tnip1结合来抑制鼠伤寒沙门氏菌介导的细胞焦亡。
Sci Rep. 2025 Feb 25;15(1):6713. doi: 10.1038/s41598-025-91296-2.
6
Natural Product-Derived Compounds Targeting Keratinocytes and Molecular Pathways in Psoriasis Therapeutics.天然产物衍生化合物在银屑病治疗中靶向角质形成细胞和分子途径。
Int J Mol Sci. 2024 May 31;25(11):6068. doi: 10.3390/ijms25116068.
7
Investigating Protein-Protein Interactions of Autophagy-Involved TNIP1.研究自噬相关TNIP1的蛋白质-蛋白质相互作用。
Methods Mol Biol. 2025;2879:63-82. doi: 10.1007/7651_2024_525.
8
Signaling pathways and targeted therapies for psoriasis.银屑病的信号通路和靶向治疗。
Signal Transduct Target Ther. 2023 Nov 27;8(1):437. doi: 10.1038/s41392-023-01655-6.
9
TNIP1 inhibits selective autophagy via bipartite interaction with LC3/GABARAP and TAX1BP1.TNIP1 通过与 LC3/GABARAP 和 TAX1BP1 的二聚体相互作用抑制选择性自噬。
Mol Cell. 2023 Mar 16;83(6):927-941.e8. doi: 10.1016/j.molcel.2023.02.023. Epub 2023 Mar 9.
10
Analysis of selected genetic variants in psoriasis susceptibility and response to treatment.银屑病易感性及治疗反应中选定基因变异的分析。
Postepy Dermatol Alergol. 2022 Oct;39(5):934-939. doi: 10.5114/ada.2022.120885. Epub 2022 Nov 9.
A20 和 ABIN 家族蛋白在类风湿关节炎患者成纤维样滑膜细胞中的促炎作用。
Immunol Lett. 2012 Jan 30;141(2):246-53. doi: 10.1016/j.imlet.2011.10.011. Epub 2011 Nov 9.
4
A20-binding inhibitor of NF-κB (ABIN1) controls Toll-like receptor-mediated CCAAT/enhancer-binding protein β activation and protects from inflammatory disease.A20 结合 NF-κB 的抑制剂 (ABIN1) 控制 Toll 样受体介导的 CCAAT/增强子结合蛋白 β 的激活并防止炎症性疾病。
Proc Natl Acad Sci U S A. 2011 Nov 1;108(44):E998-1006. doi: 10.1073/pnas.1106232108. Epub 2011 Oct 19.
5
PPARγ and NF-κB regulate the gene promoter activity of their shared repressor, TNIP1.过氧化物酶体增殖物激活受体γ(PPARγ)和核因子κB(NF-κB)调节其共同抑制因子TNIP1的基因启动子活性。
Biochim Biophys Acta. 2012 Jan;1819(1):1-15. doi: 10.1016/j.bbagrm.2011.09.006. Epub 2011 Oct 7.
6
TNIP1 is a corepressor of agonist-bound PPARs.TNIP1 是激动剂结合的 PPARs 的核心抑制剂。
Arch Biochem Biophys. 2011 Dec 1;516(1):58-66. doi: 10.1016/j.abb.2011.08.014. Epub 2011 Sep 22.
7
Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis.全基因组扫描鉴定 TNIP1、PSORS1C1 和 RHOB 为系统性硬化症的新的风险基因座。
PLoS Genet. 2011 Jul;7(7):e1002091. doi: 10.1371/journal.pgen.1002091. Epub 2011 Jul 7.
8
Confirmation of TNIP1 and IL23A as susceptibility loci for psoriatic arthritis.确认 TNIP1 和 IL23A 是银屑病关节炎的易感基因位点。
Ann Rheum Dis. 2011 Sep;70(9):1641-4. doi: 10.1136/ard.2011.150102. Epub 2011 May 29.
9
Polyubiquitin binding to ABIN1 is required to prevent autoimmunity.多泛素与 ABIN1 的结合对于预防自身免疫是必需的。
J Exp Med. 2011 Jun 6;208(6):1215-28. doi: 10.1084/jem.20102177. Epub 2011 May 23.
10
Efficacy and safety of oral retinoids in different psoriasis subtypes: a systematic literature review.口服维 A 酸类药物治疗不同银屑病亚型的疗效和安全性:系统文献回顾。
J Eur Acad Dermatol Venereol. 2011 May;25 Suppl 2:28-33. doi: 10.1111/j.1468-3083.2011.03993.x.