• 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

细胞迁移:概述

Cell migration: an overview.

作者信息

Vicente-Manzanares Miguel, Horwitz Alan Rick

机构信息

Department of Cell Biology, University of Virginia School of Medicine, Charlottesville, VA, USA.

出版信息

Methods Mol Biol. 2011;769:1-24. doi: 10.1007/978-1-61779-207-6_1.

DOI:10.1007/978-1-61779-207-6_1
PMID:21748665
Abstract

Cell migration is a fundamental process that controls morphogenesis and inflammation. Its deregulation causes or is part of many diseases, including autoimmune syndromes, chronic inflammation, mental retardation, and cancer. Cell migration is an integral part of the cell biology, embryology, immunology, and neuroscience fields; as such, it has benefited from quantum leaps in molecular biology, biochemistry, and imaging techniques, and the emergence of the genomic and proteomic era. Combinations of these techniques have revealed new and exciting insights that explain how cells adhere and move, how the migration of multiple cells are coordinated and regulated, and how the cells interact with neighboring cells and/or react to changes in their microenvironment. This introduction provides a primer of the molecular and cellular insights, particularly the signaling networks, which control the migration of individual cells as well as collective migrations. The rest of the chapters are devoted to describe in detail some of the most salient technical advances that have illuminated the field of cell migration in recent years.

摘要

细胞迁移是一个控制形态发生和炎症的基本过程。其失调会导致许多疾病或成为这些疾病的一部分,包括自身免疫综合征、慢性炎症、智力迟钝和癌症。细胞迁移是细胞生物学、胚胎学、免疫学和神经科学领域不可或缺的一部分;因此,它受益于分子生物学、生物化学和成像技术的巨大飞跃,以及基因组和蛋白质组时代的出现。这些技术的结合揭示了新的、令人兴奋的见解,解释了细胞如何黏附与移动、多个细胞的迁移如何协调与调控,以及细胞如何与邻近细胞相互作用和/或对其微环境的变化做出反应。本引言提供了分子和细胞见解的入门知识,特别是信号网络,其控制单个细胞的迁移以及集体迁移。其余各章致力于详细描述近年来阐明细胞迁移领域的一些最显著的技术进展。

相似文献

1
Cell migration: an overview.细胞迁移:概述
Methods Mol Biol. 2011;769:1-24. doi: 10.1007/978-1-61779-207-6_1.
2
Degrading devices: invadosomes in proteolytic cell invasion.降解装置:蛋白酶体在细胞侵袭中的作用
Annu Rev Cell Dev Biol. 2011;27:185-211. doi: 10.1146/annurev-cellbio-092910-154216. Epub 2011 Jul 21.
3
Cell matrix adhesion in cell migration.细胞在迁移过程中与细胞基质的黏附。
Essays Biochem. 2019 Oct 31;63(5):535-551. doi: 10.1042/EBC20190012.
4
Cell-matrix adhesion complexes: master control machinery of cell migration.细胞-基质黏附复合体:细胞迁移的主控机制
Semin Cancer Biol. 2008 Feb;18(1):65-76. doi: 10.1016/j.semcancer.2007.10.001. Epub 2007 Oct 6.
5
MyTH4-FERM myosins in the assembly and maintenance of actin-based protrusions.MyTH4-FERM肌球蛋白在基于肌动蛋白的突起的组装和维持中发挥作用。
Curr Opin Cell Biol. 2017 Feb;44:68-78. doi: 10.1016/j.ceb.2016.10.002. Epub 2016 Nov 9.
6
Running with neighbors: coordinating cell migration and cell-cell adhesion.与邻居同行:协调细胞迁移与细胞间黏附
Curr Opin Cell Biol. 2015 Oct;36:62-70. doi: 10.1016/j.ceb.2015.07.004. Epub 2015 Jul 17.
7
Regulation of cortical actin networks in cell migration.细胞迁移过程中皮质肌动蛋白网络的调控。
Int Rev Cytol. 2003;229:245-86. doi: 10.1016/s0074-7696(03)29006-9.
8
T-Plastin reinforces membrane protrusions to bridge matrix gaps during cell migration.T 型肌动蛋白稳固质膜突起以在细胞迁移过程中连接基质间隙。
Nat Commun. 2020 Sep 23;11(1):4818. doi: 10.1038/s41467-020-18586-3.
9
Cell-cell and cell-extracellular matrix adhesions cooperate to organize actomyosin networks and maintain force transmission during dorsal closure.细胞间和细胞与细胞外基质的黏附相互协作,在背侧闭合过程中组织肌动球蛋白网络并维持力的传递。
Mol Biol Cell. 2017 May 15;28(10):1301-1310. doi: 10.1091/mbc.E17-01-0033. Epub 2017 Mar 22.
10
Asymmetric Stratification-Induced Polarity Loss and Coordinated Individual Cell Movements Drive Directional Migration of Vertebrate Epithelium.非对称分层诱导极性丧失和协调的单个细胞运动驱动脊椎动物上皮的定向迁移。
Cell Rep. 2020 Oct 13;33(2):108246. doi: 10.1016/j.celrep.2020.108246.

引用本文的文献

1
Controlling Cell Migratory Patterns Under an Electric Field Regulated by a Neural Network-Based Feedback Controller.通过基于神经网络的反馈控制器调节电场来控制细胞迁移模式。
Bioengineering (Basel). 2025 Jun 20;12(7):678. doi: 10.3390/bioengineering12070678.
2
Survivin modulates stiffness-induced vascular smooth muscle cell motility.生存素调节硬度诱导的血管平滑肌细胞运动。
APL Bioeng. 2025 Jun 4;9(2):026120. doi: 10.1063/5.0252766. eCollection 2025 Jun.
3
Survivin modulates stiffness-induced vascular smooth muscle cell motility.
存活素调节硬度诱导的血管平滑肌细胞运动。
bioRxiv. 2024 Dec 12:2024.12.11.628062. doi: 10.1101/2024.12.11.628062.
4
TRPC3-mediated NFATc1 calcium signaling promotes triple negative breast cancer migration through regulating glypican-6 and focal adhesion.TRPC3介导的NFATc1钙信号通过调节磷脂酰肌醇蛋白聚糖-6和粘着斑促进三阴性乳腺癌迁移。
Pflugers Arch. 2025 Feb;477(2):253-272. doi: 10.1007/s00424-024-03030-y. Epub 2024 Oct 22.
5
Multi-omics analysis to reveal the synergistic mechanism underlying the multiple ingredients of extract on rheumatoid arthritis through the PI3K/Akt signaling pathway.多组学分析以揭示提取物的多种成分通过PI3K/Akt信号通路对类风湿关节炎发挥作用的协同机制。
Front Pharmacol. 2024 Aug 16;15:1447283. doi: 10.3389/fphar.2024.1447283. eCollection 2024.
6
Patient-specific colorectal-cancer-associated fibroblasts modulate tumor microenvironment mechanics.患者特异性结直肠癌相关成纤维细胞调节肿瘤微环境力学。
iScience. 2024 May 21;27(6):110060. doi: 10.1016/j.isci.2024.110060. eCollection 2024 Jun 21.
7
The dysadherin/FAK axis promotes individual cell migration in colon cancer.黏着斑失巢蛋白/粘着斑激酶轴促进结肠癌中单个细胞的迁移。
Int J Biol Sci. 2024 Apr 8;20(7):2356-2369. doi: 10.7150/ijbs.86699. eCollection 2024.
8
PIEZO1 regulates leader cell formation and cellular coordination during collective keratinocyte migration.PIEZO1 调节角质形成细胞集体迁移过程中的领头细胞形成和细胞协调。
PLoS Comput Biol. 2024 Apr 5;20(4):e1011855. doi: 10.1371/journal.pcbi.1011855. eCollection 2024 Apr.
9
Oleanolic acid rescues critical features of umbilical vein endothelial cells permanently affected by hyperglycemia.齐墩果酸挽救了高血糖永久影响的脐静脉内皮细胞的关键特征。
Front Endocrinol (Lausanne). 2023 Dec 13;14:1308606. doi: 10.3389/fendo.2023.1308606. eCollection 2023.
10
Biomaterial composed of chitosan, riboflavin, and hydroxyapatite for bone tissue regeneration.壳聚糖、核黄素和羟基磷灰石组成的生物材料,用于骨组织再生。
Sci Rep. 2023 Oct 9;13(1):17004. doi: 10.1038/s41598-023-44225-0.