• 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

通过解整合素金属蛋白酶微调细胞迁移

Fine Tuning Cell Migration by a Disintegrin and Metalloproteinases.

作者信息

Dreymueller D, Theodorou K, Donners M, Ludwig A

机构信息

Institute of Pharmacology and Toxicology, Uniklinik RWTH Aachen, Aachen, Germany.

Department of Pathology, Maastricht University, LK Maastricht, Netherlands.

出版信息

Mediators Inflamm. 2017;2017:9621724. doi: 10.1155/2017/9621724. Epub 2017 Feb 5.

DOI:10.1155/2017/9621724
PMID:28260841
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5316459/
Abstract

Cell migration is an instrumental process involved in organ development, tissue homeostasis, and various physiological processes and also in numerous pathologies. Both basic cell migration and migration towards chemotactic stimulus consist of changes in cell polarity and cytoskeletal rearrangement, cell detachment from, invasion through, and reattachment to their neighboring cells, and numerous interactions with the extracellular matrix. The different steps of immune cell, tissue cell, or cancer cell migration are tightly coordinated in time and place by growth factors, cytokines/chemokines, adhesion molecules, and receptors for these ligands. This review describes how a disintegrin and metalloproteinases interfere with several steps of cell migration, either by proteolytic cleavage of such molecules or by functions independent of proteolytic activity.

摘要

细胞迁移是一个重要过程,参与器官发育、组织稳态以及各种生理过程,同时也涉及众多病理过程。基本的细胞迁移以及向趋化刺激的迁移都包括细胞极性变化和细胞骨架重排、细胞与相邻细胞的脱离、侵入以及重新附着,以及与细胞外基质的众多相互作用。免疫细胞、组织细胞或癌细胞迁移的不同步骤在时间和空间上通过生长因子、细胞因子/趋化因子、黏附分子以及这些配体的受体紧密协调。本综述描述了去整合素和金属蛋白酶如何通过对这些分子的蛋白水解切割或通过独立于蛋白水解活性的功能来干扰细胞迁移的几个步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a6/5316459/0be2d383b989/MI2017-9621724.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a6/5316459/0be2d383b989/MI2017-9621724.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1a6/5316459/0be2d383b989/MI2017-9621724.001.jpg

相似文献

1
Fine Tuning Cell Migration by a Disintegrin and Metalloproteinases.通过解整合素金属蛋白酶微调细胞迁移
Mediators Inflamm. 2017;2017:9621724. doi: 10.1155/2017/9621724. Epub 2017 Feb 5.
2
Heparin-binding epidermal growth factor-like growth factor (HB-EGF) and proteolytic processing by a disintegrin and metalloproteinases (ADAM): a regulator of several pathways.肝素结合表皮生长因子样生长因子(HB-EGF)和金属蛋白酶(ADAM)的蛋白水解处理:几种途径的调节剂。
Semin Cell Dev Biol. 2014 Apr;28:22-30. doi: 10.1016/j.semcdb.2014.03.004. Epub 2014 Mar 25.
3
Therapeutic benefits from targeting of ADAM family members.靶向ADAM家族成员的治疗益处。
Biochemistry. 2004 Jun 15;43(23):7227-35. doi: 10.1021/bi049677f.
4
Fine-Tuning Limited Proteolysis: A Major Role for Regulated Site-Specific O-Glycosylation.精细调控有限蛋白水解:受调控的位点特异性 O-糖基化的主要作用。
Trends Biochem Sci. 2018 Apr;43(4):269-284. doi: 10.1016/j.tibs.2018.02.005. Epub 2018 Mar 2.
5
Breaking up the tie: disintegrin-like metalloproteinases as regulators of cell migration in inflammation and invasion.打破束缚:类整合素金属蛋白酶作为炎症和侵袭中细胞迁移的调节因子
Pharmacol Ther. 2006 Sep;111(3):985-1006. doi: 10.1016/j.pharmthera.2006.02.009. Epub 2006 Apr 19.
6
Recombinant disintegrin domain of human ADAM9 inhibits migration and invasion of DU145 prostate tumor cells.人ADAM9的重组去整合素结构域抑制DU145前列腺肿瘤细胞的迁移和侵袭。
Cell Adh Migr. 2015;9(4):293-9. doi: 10.4161/19336918.2014.994917. Epub 2015 Jul 25.
7
Girdin, an actin-binding protein, is critical for migration, adhesion, and invasion of human glioblastoma cells.Girdin是一种肌动蛋白结合蛋白,对人胶质母细胞瘤细胞的迁移、黏附和侵袭至关重要。
J Neurochem. 2014 Nov;131(4):457-69. doi: 10.1111/jnc.12831. Epub 2014 Aug 12.
8
Cell motility and cytoskeletal regulation in invasion and metastasis.侵袭和转移过程中的细胞运动及细胞骨架调控
J Mammary Gland Biol Neoplasia. 2007 Sep;12(2-3):143-52. doi: 10.1007/s10911-007-9046-4.
9
Molecular mechanisms governing thymocyte migration: combined role of chemokines and extracellular matrix.调控胸腺细胞迁移的分子机制:趋化因子与细胞外基质的联合作用
J Leukoc Biol. 2004 Jun;75(6):951-61. doi: 10.1189/jlb.1003455. Epub 2004 Mar 12.
10
Clipping, shedding and RIPping keep immunity on cue.修剪、脱落和RNA诱导沉默使免疫保持在适当状态。
Trends Immunol. 2008 Feb;29(2):75-82. doi: 10.1016/j.it.2007.10.009. Epub 2008 Jan 7.

引用本文的文献

1
Regulation of ADAM10 activity through microdomain-dependent intracellular calcium changes.通过微域依赖的细胞内钙变化来调节 ADAM10 的活性。
Cell Commun Signal. 2024 Nov 4;22(1):531. doi: 10.1186/s12964-024-01891-5.
2
Phenotype Compensation in Reproductive ADAM Gene Family: A Case Study with ADAM27 Knockout Mouse.生殖相关ADAM基因家族中的表型补偿:以ADAM27基因敲除小鼠为例的研究
Iran J Biotechnol. 2022 Oct 1;20(4):e2902. doi: 10.30498/ijb.2022.250175.2902. eCollection 2022 Oct.
3
Endothelial ADAM10 controls cellular response to oxLDL and its deficiency exacerbates atherosclerosis with intraplaque hemorrhage and neovascularization in mice.

本文引用的文献

1
A disintegrin and metalloproteinase (ADAM)-10 as a predictive factor for tocilizumab effectiveness in rheumatoid arthritis.作为托珠单抗治疗类风湿关节炎有效性预测因子的解聚素和金属蛋白酶(ADAM)-10
Mod Rheumatol. 2017 Sep;27(5):782-786. doi: 10.1080/14397595.2016.1256025. Epub 2016 Dec 23.
2
Metalloproteinases ADAM10 and ADAM17 Mediate Migration and Differentiation in Glioblastoma Sphere-Forming Cells.金属蛋白酶ADAM10和ADAM17介导胶质母细胞瘤成球细胞的迁移和分化。
Mol Neurobiol. 2017 Jul;54(5):3893-3905. doi: 10.1007/s12035-016-0053-6. Epub 2016 Aug 19.
3
Considerations on inhibition approaches for proinflammatory functions of ADAM proteases.
内皮细胞的ADAM10控制细胞对氧化型低密度脂蛋白的反应,其缺失会加剧小鼠动脉粥样硬化并伴有斑块内出血和新生血管形成。
Front Cardiovasc Med. 2023 Jan 27;10:974918. doi: 10.3389/fcvm.2023.974918. eCollection 2023.
4
ADAM17-mediated EGFR ligand shedding directs macrophage-promoted cancer cell invasion.ADAM17 介导的 EGFR 配体脱落指导巨噬细胞促进癌细胞侵袭。
JCI Insight. 2022 Sep 22;7(18):e155296. doi: 10.1172/jci.insight.155296.
5
Local delivery of interleukin 7 with an oncolytic adenovirus activates tumor-infiltrating lymphocytes and causes tumor regression.局部递送白细胞介素 7 联合溶瘤腺病毒激活肿瘤浸润淋巴细胞并引起肿瘤消退。
Oncoimmunology. 2022 Jul 12;11(1):2096572. doi: 10.1080/2162402X.2022.2096572. eCollection 2022.
6
Matrix Metalloproteinases in Chemoresistance: Regulatory Roles, Molecular Interactions, and Potential Inhibitors.化学抗性中的基质金属蛋白酶:调节作用、分子相互作用及潜在抑制剂
J Oncol. 2022 May 9;2022:3249766. doi: 10.1155/2022/3249766. eCollection 2022.
7
(Wall.) Seem Improves Intimal Hyperplasia after Vascular Injury by Downregulating the Wnt3/Dvl-1/-Catenin Pathway.(Wall 等人)通过下调 Wnt3/Dvl-1/-Catenin 通路,似乎改善了血管损伤后的内膜增生。
Biomed Res Int. 2021 Jul 12;2021:6682525. doi: 10.1155/2021/6682525. eCollection 2021.
8
Stromal Protein-Mediated Immune Regulation in Digestive Cancers.基质蛋白介导的消化系统癌症免疫调节
Cancers (Basel). 2021 Jan 5;13(1):146. doi: 10.3390/cancers13010146.
9
A Disintegrin and Metalloproteinase-Control Elements in Infectious Diseases.感染性疾病中的解整合素和金属蛋白酶控制元件
Front Cardiovasc Med. 2020 Dec 16;7:608281. doi: 10.3389/fcvm.2020.608281. eCollection 2020.
10
Blocking ADAM17 Function with a Monoclonal Antibody Improves Sepsis Survival in a Murine Model of Polymicrobial Sepsis.单克隆抗体阻断 ADAM17 功能可改善多微生物脓毒症小鼠模型的脓毒症存活率。
Int J Mol Sci. 2020 Sep 12;21(18):6688. doi: 10.3390/ijms21186688.
关于ADAM蛋白酶促炎功能抑制方法的思考
Platelets. 2017 Jun;28(4):354-361. doi: 10.1080/09537104.2016.1203396. Epub 2016 Jul 26.
4
A novel peptide ADAM8 inhibitor attenuates bronchial hyperresponsiveness and Th2 cytokine mediated inflammation of murine asthmatic models.一种新型肽类ADAM8抑制剂可减轻小鼠哮喘模型的支气管高反应性和Th2细胞因子介导的炎症。
Sci Rep. 2016 Jul 26;6:30451. doi: 10.1038/srep30451.
5
ADAM10-Dependent Signaling Through Notch1 and Notch4 Controls Development of Organ-Specific Vascular Beds.通过Notch1和Notch4的ADAM10依赖性信号传导控制器官特异性血管床的发育。
Circ Res. 2016 Aug 5;119(4):519-31. doi: 10.1161/CIRCRESAHA.115.307738. Epub 2016 Jun 27.
6
ADAM17-siRNA inhibits MCF-7 breast cancer through EGFR-PI3K-AKT activation.ADAM17小干扰RNA通过激活表皮生长因子受体-磷脂酰肌醇-3激酶-蛋白激酶B抑制MCF-7乳腺癌细胞。
Int J Oncol. 2016 Aug;49(2):682-90. doi: 10.3892/ijo.2016.3536. Epub 2016 May 24.
7
ADAM and ADAMTS Family Proteins and Snake Venom Metalloproteinases: A Structural Overview.ADAM和ADAMTS家族蛋白与蛇毒金属蛋白酶:结构概述。
Toxins (Basel). 2016 May 17;8(5):155. doi: 10.3390/toxins8050155.
8
Phosphatidylserine exposure is required for ADAM17 sheddase function.磷脂酰丝氨酸暴露是 ADAM17 剪切酶功能所必需的。
Nat Commun. 2016 May 10;7:11523. doi: 10.1038/ncomms11523.
9
A Disintegrin and Metalloprotease (ADAM): Historical Overview of Their Functions.解整合素金属蛋白酶(ADAM):其功能的历史概述
Toxins (Basel). 2016 Apr 23;8(4):122. doi: 10.3390/toxins8040122.
10
Regulation of Receptor for Advanced Glycation End Products (RAGE) Ectodomain Shedding and Its Role in Cell Function.晚期糖基化终末产物受体(RAGE)胞外域脱落的调控及其在细胞功能中的作用。
J Biol Chem. 2016 Jun 3;291(23):12057-73. doi: 10.1074/jbc.M115.702399. Epub 2016 Mar 28.