Adjustable viscoelasticity allows for efficient collective cell migration

被引:93
作者
Barriga, Elias H. [1 ]
Mayor, Roberto [1 ]
机构
[1] UCL, Dept Cell & Dev Biol, London WC1E 6BT, England
基金
英国医学研究理事会; 英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
Collective migration; Viscoelasticity; Adherens junctions; EMT; Mechanical microenvironment; Cancer invasion; EPITHELIAL-MESENCHYMAL TRANSITION; N-CADHERIN; ACTIN DYNAMICS; MECHANICAL-PROPERTIES; FORCE TRANSMISSION; ENDOTHELIAL-CELLS; NUCLEAR MECHANICS; MOLECULAR CONTROL; FOCAL ADHESIONS; TISSUE TENSION;
D O I
10.1016/j.semcdb.2018.05.027
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Cell migration is essential for a wide range of biological processes such as embryo morphogenesis, wound healing, regeneration, and also in pathological conditions, such as cancer. In such contexts, cells are required to migrate as individual entities or as highly coordinated collectives, both of which requiring cells to respond to molecular and mechanical cues from their environment. However, whilst the function of chemical cues in cell migration is comparatively well understood, the role of tissue mechanics on cell migration is just starting to be studied. Recent studies suggest that the dynamic tuning of the viscoelasticity within a migratory cluster of cells, and the adequate elastic properties of its surrounding tissues, are essential to allow efficient collective cell migration in vivo. In this review we focus on the role of viscoelasticity in the control of collective cell migration in various cellular systems, mentioning briefly some aspects of single cell migration. We aim to provide details on how viscoelasticity of collectively migrating groups of cells and their surroundings is adjusted to ensure correct morphogenesis, wound healing, and metastasis. Finally, we attempt to show that environmental viscoelasticity triggers molecular changes within migrating clusters and that these new molecular setups modify clusters' viscoelasticity, ultimately allowing them to migrate across the challenging geometries of their microenvironment. (C) 2018 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:55 / 68
页数:14
相关论文
共 227 条
[1]
Chemokine triggered integrin activation and actin remodeling events guiding lymphocyte migration across vascular barriers [J].
Alon, Ronen ;
Shulman, Ziv .
EXPERIMENTAL CELL RESEARCH, 2011, 317 (05) :632-641
[2]
EMT: 2016 [J].
Angela Nieto, M. ;
Huang, Ruby Yun-Ju ;
Jackson, Rebecca A. ;
Thiery, Jean Paul .
CELL, 2016, 166 (01) :21-45
[3]
EMT or EMT-promoting transcription factors, where to focus the light? [J].
Ansieau, Stephane ;
Colli, Guillaume ;
Hill, Louise .
FRONTIERS IN ONCOLOGY, 2014, 4
[4]
PDGF controls contact inhibition of locomotion by regulating N-cadherin during neural crest migration [J].
Bahm, Isabel ;
Barriga, Elias H. ;
Frolov, Antonina ;
Theveneau, Eric ;
Frankel, Paul ;
Mayor, Roberto .
DEVELOPMENT, 2017, 144 (13) :2456-2468
[5]
Tissue stiffening coordinates morphogenesis by triggering collective cell migration in vivo [J].
Barriga, Elias H. ;
Franze, Kristian ;
Charras, Guillaume ;
Mayor, Roberto .
NATURE, 2018, 554 (7693) :523-+
[6]
Embryonic Cell-Cell Adhesion: A Key Player in Collective Neural Crest Migration [J].
Barriga, Elias H. ;
Mayor, Roberto .
CELLULAR ADHESION IN DEVELOPMENT AND DISEASE, 2015, 112 :301-+
[7]
The hypoxia factor Hif-1α controls neural crest chemotaxis and epithelial to mesenchymal transition [J].
Barriga, Elias H. ;
Maxwell, Patrick H. ;
Reyes, Ariel E. ;
Mayor, Roberto .
JOURNAL OF CELL BIOLOGY, 2013, 201 (05) :759-776
[8]
Dynamics of adherens junctions in epithelial establishment, maintenance, and remodeling [J].
Baum, Buzz ;
Georgiou, Marios .
JOURNAL OF CELL BIOLOGY, 2011, 192 (06) :907-917
[9]
Measurement of local viscoelasticity and forces in living cells by magnetic tweezers [J].
Bausch, AR ;
Möller, W ;
Sackmann, E .
BIOPHYSICAL JOURNAL, 1999, 76 (01) :573-579
[10]
Control of cell-cell forces and collective cell dynamics by the intercellular adhesome [J].
Bazellieres, Elsa ;
Conte, Vito ;
Elosegui-Artola, Alberto ;
Serra-Picamal, Xavier ;
Bintanel-Morcillo, Maria ;
Roca-Cusachs, Pere ;
Munoz, Jose J. ;
Sales-Pardo, Marta ;
Guimera, Roger ;
Trepat, Xavier .
NATURE CELL BIOLOGY, 2015, 17 (04) :409-+