• 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

由肿瘤坏死因子受体(TNFR)家族的死亡受体激活的信号传导。

Signaling activated by the death receptors of the TNFR family.

作者信息

Andera Ladislav

机构信息

Institute of Molecular Genetics AS CR, Videnska, Prague, Czech Republic.

出版信息

Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2009 Sep;153(3):173-80. doi: 10.5507/bp.2009.029.

DOI:10.5507/bp.2009.029
PMID:19851428
Abstract

BACKGROUND

The fine balance in cellular life and death is affected by a number of tightly regulated, direct signals that can help to turn the balance either in favor of or against the ultimate fate. Among the most prominent players in the field of the extracellular signals leading to cell death, preferentially through induction of apoptosis belong several receptors from so-called Death Receptors group of the Tumour Necrosis Factors Receptors (TNFR) family.

METHODS AND RESULTS

Over 15 years of the research on activation and regulation of the most prominent member of this group - receptors for the ligands TRAIL, FasL and TNFalpha brought not only a detail (and still refining) mechanism of these receptors activation and downstream signaling, but also connected them with the ultimate apoptotic gatekeeper - mitochondria. Mitochondria are, in addition to their essential role as the energy factories also repositories of a cavalry of apoptosis-inducing as well as regulatory proteins. However, in addition to the pro-death signaling, these receptors were also shown under certain circumstances to activate an opposite, pro-proliferative signaling as well as to participate in pro-inflammatory responses.

CONCLUSIONS

Thus despite the concerned effort of a number of groups and thousands of published papers, novel roles for the intriguing group of these receptors and their ligands and fine tuning of their signaling still await to be uncovered. This cut-through review will be mainly focused on the prominent death-inducing members of this group - TNFR1, Fas/CD95 and TRAIL receptors.

摘要

背景

细胞生死的微妙平衡受到许多严格调控的直接信号的影响,这些信号可有助于使平衡朝着有利于或不利于最终命运的方向转变。在导致细胞死亡的细胞外信号领域中,最突出的参与者之一是肿瘤坏死因子受体(TNFR)家族中所谓死亡受体组的几种受体,它们优先通过诱导细胞凋亡发挥作用。

方法与结果

对该组中最突出成员——TRAIL、FasL和TNFα配体的受体进行了超过15年的激活和调控研究,不仅揭示了这些受体激活和下游信号传导的详细(且仍在完善)机制,还将它们与最终的凋亡守门人——线粒体联系起来。线粒体除了作为能量工厂发挥重要作用外,还是一系列凋亡诱导蛋白和调节蛋白的储存库。然而,除了促死亡信号传导外,这些受体在某些情况下还被证明可激活相反的促增殖信号传导,并参与促炎反应。

结论

因此,尽管许多研究团队付出了努力且发表了数千篇论文,但这些受体及其配体这一有趣的群体的新作用以及它们信号传导的精细调节仍有待发现。本综述将主要聚焦于该组中突出的诱导死亡成员——TNFR1、Fas/CD95和TRAIL受体。

相似文献

1
Signaling activated by the death receptors of the TNFR family.由肿瘤坏死因子受体(TNFR)家族的死亡受体激活的信号传导。
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2009 Sep;153(3):173-80. doi: 10.5507/bp.2009.029.
2
Life and death by death receptors.死亡受体介导的生死抉择
FASEB J. 2009 Jun;23(6):1625-37. doi: 10.1096/fj.08-111005. Epub 2009 Jan 13.
3
Structural determinants of DISC function: new insights into death receptor-mediated apoptosis signalling.结构决定 DISC 的功能:死亡受体介导的细胞凋亡信号转导的新见解。
Pharmacol Ther. 2013 Nov;140(2):186-99. doi: 10.1016/j.pharmthera.2013.06.009. Epub 2013 Jul 8.
4
Subcellular compartmentalization of TNF receptor-1 and CD95 signaling pathways.TNF 受体-1 和 CD95 信号通路的亚细胞区室化。
Eur J Cell Biol. 2011 Jun-Jul;90(6-7):467-75. doi: 10.1016/j.ejcb.2010.11.002. Epub 2010 Dec 7.
5
The FLIP Side of Life.生活的另一面。
Sci Signal. 2013 Jan 15;6(258):pe2. doi: 10.1126/scisignal.2003845.
6
The role of TRADD in death receptor signaling.TRADD 在死亡受体信号转导中的作用。
Cell Cycle. 2012 Mar 1;11(5):871-6. doi: 10.4161/cc.11.5.19300.
7
A novel synthetic analogue of ω-3 17,18-epoxyeicosatetraenoic acid activates TNF receptor-1/ASK1/JNK signaling to promote apoptosis in human breast cancer cells.一种新型ω-3 17,18-环氧二十碳四烯酸合成类似物激活肿瘤坏死因子受体-1/凋亡信号调节激酶1/应激活化蛋白激酶信号通路,以促进人乳腺癌细胞凋亡。
FASEB J. 2017 Dec;31(12):5246-5257. doi: 10.1096/fj.201700033R. Epub 2017 Aug 10.
8
Apo-3, a new member of the tumor necrosis factor receptor family, contains a death domain and activates apoptosis and NF-kappa B.Apo-3是肿瘤坏死因子受体家族的新成员,含有一个死亡结构域,并能激活细胞凋亡和核因子κB。
Curr Biol. 1996 Dec 1;6(12):1669-76. doi: 10.1016/s0960-9822(02)70791-4.
9
Synthetic peptides corresponding to ligand-binding region of death receptors, DR5, Fas, and TNFR, specifically inhibit cell death mediated by the death ligands, respectively.与死亡受体DR5、Fas和TNFR的配体结合区域相对应的合成肽分别特异性抑制由死亡配体介导的细胞死亡。
Biochim Biophys Acta. 2004 Jun 1;1699(1-2):131-7. doi: 10.1016/j.bbapap.2004.02.016.
10
Apo2L/TRAIL-dependent recruitment of endogenous FADD and caspase-8 to death receptors 4 and 5.Apo2L/TRAIL 依赖性地将内源性 FADD 和半胱天冬酶 -8 募集至死亡受体 4 和 5。
Immunity. 2000 Jun;12(6):611-20. doi: 10.1016/s1074-7613(00)80212-5.

引用本文的文献

1
Different Ways to Die: Cell Death Pathways and Their Association With Spinal Cord Injury.死亡的不同方式:细胞死亡途径及其与脊髓损伤的关联
Neurospine. 2023 Jun;20(2):430-448. doi: 10.14245/ns.2244976.488. Epub 2023 Mar 2.
2
Lymphotoxins Serve as a Novel Orchestrator in T1D Pathogenesis.淋巴毒素在 T1D 发病机制中充当新型协调因子。
Front Immunol. 2022 Jun 9;13:917577. doi: 10.3389/fimmu.2022.917577. eCollection 2022.
3
Mechanism of Ferroptosis and Its Role in Spinal Cord Injury.铁死亡的机制及其在脊髓损伤中的作用
Front Neurol. 2022 Jun 9;13:926780. doi: 10.3389/fneur.2022.926780. eCollection 2022.
4
GDF-11 Protects the Traumatically Injured Spinal Cord by Suppressing Pyroptosis and Necroptosis via TFE3-Mediated Autophagy Augmentation.GDF-11 通过 TFE3 介导的自噬增强来抑制焦亡和坏死性凋亡从而保护外伤性脊髓损伤。
Oxid Med Cell Longev. 2021 Oct 19;2021:8186877. doi: 10.1155/2021/8186877. eCollection 2021.
5
Programmed cell death in spinal cord injury pathogenesis and therapy.脊髓损伤发病机制和治疗中的程序性细胞死亡。
Cell Prolif. 2021 Mar;54(3):e12992. doi: 10.1111/cpr.12992. Epub 2021 Jan 27.
6
The Golgi Apparatus May Be a Potential Therapeutic Target for Apoptosis-Related Neurological Diseases.高尔基体可能是凋亡相关神经疾病的潜在治疗靶点。
Front Cell Dev Biol. 2020 Aug 31;8:830. doi: 10.3389/fcell.2020.00830. eCollection 2020.
7
Conformational states of TNFR1 as a molecular switch for receptor function.TNFR1 的构象状态作为受体功能的分子开关。
Protein Sci. 2020 Jun;29(6):1401-1415. doi: 10.1002/pro.3829. Epub 2020 Jan 31.
8
RIP1/RIP3-regulated necroptosis as a target for multifaceted disease therapy (Review).RIP1/RIP3 调节的坏死性凋亡作为多方面疾病治疗的靶点(综述)。
Int J Mol Med. 2019 Sep;44(3):771-786. doi: 10.3892/ijmm.2019.4244. Epub 2019 Jun 14.
9
Regulation of alveolar macrophage death in acute lung inflammation.肺泡巨噬细胞在急性肺炎症中的死亡调控。
Respir Res. 2018 Mar 27;19(1):50. doi: 10.1186/s12931-018-0756-5.
10
Molecular signaling cascades involved in nonmelanoma skin carcinogenesis.非黑色素瘤皮肤癌发生过程中涉及的分子信号级联反应。
Biochem J. 2016 Oct 1;473(19):2973-94. doi: 10.1042/BCJ20160471.