A. Akhmanova, S. J. Stehbens, and A. S. Yap, Touch, grasp, deliver and control: functional cross­talk between microtubules and cell adhesions, Traffic, vol.10, pp.268-274, 2009.
DOI : 10.1111/j.1600-0854.2008.00869.x
URL : https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1600-0854.2008.00869.x

A. Aleksandrova, A. Czirok, E. Kosa, O. Galkin, T. J. Cheuvront et al., The endoderm and myocardium join forces to drive early heart tube assembly, Dev Biol, vol.404, pp.40-54, 2015.

M. Aragona, T. Panciera, A. Manfrin, S. Giulitti, F. Michielin et al., A mechanical checkpoint controls multicellu­ lar growth through YAP/TAZ regulation by actin­processing factors, Cell, vol.154, pp.1047-1059, 2013.
DOI : 10.1016/j.cell.2013.07.042
URL : https://doi.org/10.1016/j.cell.2013.07.042

G. Aranjuez, A. Burtscher, K. Sawant, P. Majumder, and J. A. Mcdonald, Dynamic myosin activation promotes collective morphology and migra­ tion by locally balancing oppositional forces from surrounding tissue, Mol Biol Cell, vol.27, pp.1898-1910, 2016.
DOI : 10.1091/mbc.e15-10-0744
URL : http://europepmc.org/articles/pmc4907723?pdf=render

P. Atherton, B. Stutchbury, D. Jethwa, and C. Ballestrem, Mechanosensitive components of integrin adhesions: role of vinculin, Exp Cell Res, vol.343, pp.21-27, 2016.

V. Auernheimer, L. A. Lautscham, M. Leidenberger, O. Friedrich, B. Kappes et al., Vinculin phosphorylation at residues Y100 and Y1065 is required for cellular force transmission, J Cell Sci, vol.128, pp.3435-3443, 2015.
DOI : 10.1242/jcs.172031
URL : http://jcs.biologists.org/content/128/18/3435.full.pdf

K. Austen, P. Ringer, A. Mehlich, A. Chrostek­grashoff, C. Kluger et al., Mechanical linkages, Nat Cell Biol, vol.17, pp.1597-1606, 2016.

E. L. Baker, J. Lu, D. Yu, R. T. Bonnecaze, and M. H. Zaman, Cancer cell stiffness: integrated roles of three­dimensional matrix stiffness and transforming potential, Biophys J, vol.99, pp.2048-2057, 2010.

C. Bakolitsa, D. M. Cohen, L. A. Bankston, A. A. Bobkov, G. W. Cadwell et al., Structural basis for vinculin activation at sites of cell adhesion, Nature, vol.430, pp.583-586, 2004.

M. Basan, J. Elgeti, E. Hannezo, W. Rappel, and H. Levine, Alignment of cellular motility forces with tissue flow as a mechanism for efficient wound healing, Proc Natl Acad Sci, vol.110, pp.2452-2459, 2013.

E. Bazellières, V. Conte, A. Elosegui­artola, X. Serra­picamal, M. Bintanel­morcillo et al., Control of cell­cell forces and collective cell dynamics by the intercellular adhesome, Nat Cell Biol, vol.17, pp.409-420, 2015.

C. Bertocchi, Y. Wang, A. Ravasio, Y. Hara, Y. Wu et al., Nanoscale architecture of cadherin­based cell adhesions, Nat Cell Biol, vol.19, pp.28-37, 2016.
DOI : 10.1038/ncb3456
URL : http://europepmc.org/articles/pmc5421576?pdf=render

R. Bhattacharya, A. M. Gonzalez, P. J. Debiase, H. E. Trejo, R. D. Goldman et al., Recruitment of vimentin to the cell surface by beta3 integrin and plectin mediates adhesion strength, J Cell Sci, vol.122, pp.1390-1400, 2009.

J. Block, V. Schroeder, P. Pawelzyk, N. Willenbacher, and S. Köster, Physical properties of cytoplasmic intermediate filaments, Biochim Biophys Acta, vol.1853, pp.3053-3064, 2015.

N. Borghi, M. Lowndes, V. Maruthamuthu, M. L. Gardel, and W. J. Nelson, Regulation of cell motile behavior by crosstalk between cadherin­ and in­ tegrin­mediated adhesions, Proc Natl Acad Sci, vol.107, pp.13324-13329, 2010.

N. Borghi, M. Sorokina, O. G. Shcherbakova, W. I. Weis, B. L. Pruitt et al., E­cadherin is under constitutive actomyosin­generated tension that is increased at cell­cell contacts upon externally applied stretch, Proc Natl Acad Sci, vol.109, pp.12568-12573, 2012.
DOI : 10.1073/pnas.1204390109
URL : http://www.pnas.org/content/109/31/12568.full.pdf

B. P. Bouchet and A. Akhmanova, Microtubules in 3D cell motility, J Cell Sci, vol.130, pp.39-50, 2017.
DOI : 10.1242/jcs.189431
URL : http://jcs.biologists.org/content/joces/130/1/39.full.pdf

B. P. Bouchet, R. E. Gough, Y. C. Ammon, D. Van-de-willige, H. Post et al., , 2016.

, Talin­KANK1 interaction controls the recruitment of cortical microtubule stabilizing complexes to focal adhesions, Elife, vol.5, pp.1-23

P. M. Bradbury, K. Turner, C. Mitchell, K. R. Griffin, S. Middlemiss et al., The focal adhesion tar­ geting (FAT) domain of p130 Crk associated substrate (p130Cas) confers mechanosensing function, J Cell Sci, vol.130, pp.1263-1273, 2017.

R. Desai, R. Sarpal, N. Ishiyama, M. Pellikka, M. Ikura et al., Monomeric ?­catenin links cadherin to the actin cytoskeleton, Nat Cell Biol, vol.15, pp.261-273, 2013.

K. Doxzen, S. Vedula, M. C. Leong, H. Hirata, N. S. Gov et al., Guidance of cell migration by substrate dimension, Biophys J, vol.104, pp.313-321, 2013.

D. W. Dumbauld, T. T. Lee, A. Singh, J. Scrimgeour, C. A. Gersbach et al., How vinculin regulates force transmission, Proc Natl Acad Sci, vol.110, pp.9788-9793, 2013.
DOI : 10.1073/pnas.1216209110
URL : http://europepmc.org/articles/pmc3683711?pdf=render

D. W. Dumbauld, H. Shin, N. D. Gallant, K. E. Michael, H. Radhakrishna et al., Contractility modulates cell adhesion strengthening through fo­ cal adhesion kinase and assembly of vinculin­containing focal adhesions, J Cell Physiol, vol.223, pp.746-756, 2010.

I. Dupin, E. Camand, and S. Etienne­manneville, Classical cadherins control nucleus and centrosome position and cell polarity, J Cell Biol, vol.185, pp.779-786, 2009.
DOI : 10.1083/jcb.200812034
URL : http://jcb.rupress.org/content/185/5/779.full.pdf

I. Dupin, Y. Sakamoto, and S. Etienne­manneville, Cytoplasmic intermedi­ ate filaments mediate actin­driven positioning of the nucleus, J Cell Sci, vol.124, pp.865-872, 2011.

S. Dupont, L. Morsut, M. Aragona, E. Enzo, S. Giulitti et al., Role of YAP/TAZ in mechanotransduction, Nature, vol.474, pp.179-183, 2011.

O. Du-roure, A. Saez, A. Buguin, R. H. Austin, P. Chavrier et al., Force mapping in epithelial cell migration, Proc Natl Acad Sci, vol.102, pp.2390-2395, 2005.
URL : https://hal.archives-ouvertes.fr/hal-00188271

M. Dwivedi and R. Winter, Article binding of vinculin to lipid membranes in its inhibited and activated states, Biophys J, vol.111, pp.1444-1453, 2016.

M. Egeblad, M. G. Rasch, and V. M. Weaver, Dynamic interplay between the collagen scaffold and tumor evolution, Curr Opin Cell Biol, vol.22, pp.697-706, 2010.
DOI : 10.1016/j.ceb.2010.08.015
URL : http://europepmc.org/articles/pmc2948601?pdf=render

A. Elosegui­artola, R. Oria, Y. Chen, A. Kosmalska, C. Pérez­gonzález et al., Mechanical regulation of a molecular clutch defines force transmission and transduction in response to matrix rigidity, Nat Cell Biol, vol.18, pp.540-548, 2016.

A. J. Engler, C. Carag­krieger, C. P. Johnson, M. Raab, H. Tang et al., Embryonic cardiomyocytes beat best on a matrix with heart­like elasticity: scar­like rigidity inhibits beating, J Cell Sci, vol.121, pp.3794-3802, 2008.
DOI : 10.1242/jcs.029678
URL : http://jcs.biologists.org/content/121/22/3794.full.pdf

A. J. Engler, M. A. Griffin, S. Sen, C. G. Bönnemann, H. L. Sweeney et al., Myotubes differentiate optimally on substrates with tissue­like stiffness: pathological implications for soft or stiff microenvironments, J Cell Biol, vol.166, pp.877-887, 2004.

A. J. Engler, S. Sen, H. L. Sweeney, and D. E. Discher, Matrix elasticity directs stem cell lineage specification, Cell, vol.126, pp.677-689, 2006.

S. Etienne­manneville, Microtubules in cell migration, Annu Rev Cell Dev Biol, vol.29, pp.471-499, 2013.

S. Etienne­manneville, Neighborly relations during collective migra­ tion, Curr Opin Cell Biol, vol.30, pp.51-59, 2014.

P. Friedl and R. Mayor, Tuning collective cell migration by cell­cell junction regulation, Cold Spring Harb Perspect Biol, vol.9, pp.1-17, 2017.

M. L. Gardel, B. Sabass, J. L. Danuser, G. Schwarz, U. S. Waterman et al., Traction stress in focal adhesions correlates biphasically with actin retro­ grade flow speed, J Cell Biol, vol.183, pp.999-1005, 2008.

B. Geiger, K. T. Tokuyasu, A. H. Dutton, and S. J. Singer, Vinculin, an intracel­ lular protein localized at specialized sites where microfilament bundles terminate at cell membranes, Proc Natl Acad Sci, vol.77, pp.4127-4131, 1980.

S. Ghassemi, G. Meacci, S. Liu, A. A. Gondarenko, A. Mathur et al., Cells test substrate rigidity by local contrac­ tions on submicrometer pillars, Proc Natl Acad Sci, vol.109, pp.5328-5333, 2012.

M. Ghibaudo, A. Saez, L. Trichet, A. Xayaphoummine, J. Browaeys et al., Traction forces and rigidity sensing regulate cell functions, Soft Matter, vol.4, p.1836, 2008.
URL : https://hal.archives-ouvertes.fr/hal-00315437

W. H. Goldmann, Role of vinculin in cellular mechanotransduction, Cell Biol Int, vol.40, pp.241-256, 2016.

W. H. Goldmann, V. Auernheimer, I. Thievessen, and B. Fabry, Vinculin, cell mechanics and tumour cell invasion, Cell Biol Int, vol.37, pp.397-405, 2013.

J. Golji, J. Lam, and M. Mofrad, Vinculin activation is necessary for com­ plete talin binding, Biophys J, vol.100, pp.332-340, 2011.

M. Gonzales, B. Weksler, D. Tsuruta, R. D. Goldman, K. J. Yoon et al., Structure and function of a vimentin­associ­ ated matrix adhesion in endothelial cells, Mol Biol Cell, vol.12, pp.85-100, 2001.

C. Grashoff, B. D. Hoffman, M. D. Brenner, R. Zhou, M. Parsons et al., Measuring mechanical tension across vinculin reveals regulation of focal adhesion dynamics, Nature, vol.466, pp.263-266, 2010.

B. M. Gumbiner, Regulation of cadherin­mediated adhesion in mor­ phogenesis, Nat Cell Biol, vol.14, pp.1183-1197, 2005.

W. Guo, M. T. Frey, N. A. Burnham, and Y. Wang, Substrate rigidity regulates the formation and maintenance of tissues, Biophys J, vol.90, pp.2213-2220, 2006.

D. Cai, S. C. Chen, M. Prasad, L. He, X. Wang et al., Mechanical feedback through E­ cadherin promotes direction sensing during collective cell migration, Cell, vol.157, pp.1146-1159, 2014.

D. Calderwood, I. D. Campbell, and D. R. Critchley, Talins and kindlins: part­ ners in integrin­mediated adhesion, Nat Rev Mol Cell Biol, vol.14, pp.503-517, 2013.

F. Calvo, N. Ege, A. Grande­garcia, S. Hooper, R. P. Jenkins et al., Mechanotransduction and YAP­dependent matrix remodelling is required for the generation and maintenance of cancer­associated fibro­ blasts, Nat Cell Biol, vol.15, pp.637-646, 2013.

E. Camand, F. Peglion, N. Osmani, M. Sanson, and S. Etienne­manneville, N­cadherin expression level modulates integrin­mediated polarity and strongly impacts on the speed and directionality of glial cell migration, J Cell Sci, vol.125, pp.844-857, 2012.

A. Carisey, R. Tsang, A. M. Greiner, N. Nijenhuis, N. Heath et al., Vinculin regulates the recruitment and release of core focal adhesion proteins in a force­ dependent manner, Curr Biol, vol.23, pp.271-281, 2013.

L. B. Case and C. M. Waterman, Integration of actin dynamics and cell adhe­ sion by a three­dimensional, mechanosensitive molecular clutch, Nat Cell Biol, vol.17, pp.955-963, 2015.

R. P. Cavalheiro, M. A. Lima, T. R. Jarrouge­bouças, G. M. Viana, C. C. Lopes et al., Coupling of vinculin to F­actin demands Syndecan­4 proteogly­ can, Matrix Biol, vol.0945, issue.053, pp.30191-30194, 2017.

C. E. Chan and D. J. Odde, Traction dynamics of filopodia on compliant substrates, Science, vol.322, pp.1687-1691, 2008.

R. Changede and M. Sheetz, Integrin and cadherin clusters: a robust way to organize adhesions for cell mechanics, BioEssays, vol.39, pp.1-12, 2016.

R. Changede, X. Xu, F. Margadant, and M. P. Sheetz, Nascent integrin adhe­ sions form on all matrix rigidities after integrin activation, Dev Cell, vol.35, pp.614-621, 2015.

H. Chen, D. M. Choudhury, and S. W. Craig, Coincidence of actin filaments and talin is required to activate vinculin, J Biol Chem, vol.281, pp.40389-40398, 2006.

K. Chinthalapudi, D. N. Patil, E. S. Rangarajan, C. Rader, and T. Izard, Lipid­ directed vinculin dimerization, Biochemistry, vol.54, pp.2758-2768, 2015.

K. Chinthalapudi, E. S. Rangarajan, D. N. Patil, E. M. George, D. T. Brown et al., Lipid binding promotes oligomerization and focal adhesion activity of vinculin, J Cell Biol, vol.207, pp.643-656, 2014.

C. K. Choi, M. Vicente­manzanares, J. Zareno, L. A. Whitmore, A. Mogilner et al., Actin and alpha­actinin orchestrate the assembly and maturation of nascent adhesions in a myosin II motor­independent man­ ner, Nat Cell Biol, vol.10, pp.1039-1050, 2008.

D. M. Cohen, H. Chen, R. P. Johnson, B. Choudhury, and S. W. Craig, Two distinct head­tail interfaces cooperate to suppress activation of vinculin by talin, J Biol Chem, vol.280, pp.17109-17117, 2005.

J. L. Coll, A. Ben­ze'ev, R. M. Ezzell, R. Fernández, J. L. Baribault et al., Targeted disruption of vinculin genes in F9 and embryonic stem cells changes cell morphology, adhesion, and locomotion, Proc Natl Acad Sci, vol.92, pp.9161-9165, 1995.

W. A. Comrie, A. Babich, and J. K. Burkhardt, F­actin flow drives affinity matu­ ration and spatial organization of LFA­1 at the immunological synapse, J Cell Biol, vol.208, pp.475-491, 2015.

B. D. Cosgrove, K. L. Mui, T. P. Driscoll, S. R. Caliari, K. D. Mehta et al., N­cadherin adhesive interactions modulate matrix mechanosensing and fate commitment of mesenchymal stem cells, Nat Mater, vol.15, pp.1297-1306, 2016.

S. R. Coyer, A. Singh, D. W. Dumbauld, D. A. Calderwood, S. W. Craig et al., Nanopatterning reveals an ECM area threshold for focal adhesion assembly and force transmission that is regulated by integrin activation and cytoskeleton tension, J Cell Sci, vol.125, pp.5110-5123, 2012.

M. Das, S. Ithychanda, S. Qin, J. Plow, and E. F. , Mechanisms of talin­ dependent integrin signaling and crosstalk, Biochim Biophys Acta, vol.1838, pp.579-588, 2014.

T. Das, K. Safferling, S. Rausch, N. Grabe, H. Boehm et al., A molecular mechanotransduction pathway regulates collective migration of epithelial cells, Nat Cell Biol, vol.17, pp.276-287, 2015.

A. Del-rio, R. Perez­jimenez, R. Liu, P. Roca­cusachs, J. M. Fernandez et al., Stretching single talin rod molecules activates vinculin binding, Science, vol.323, pp.638-641, 2009.

M. Dembo and Y. Wang, Stresses at the cell­to­substrate interface dur­ ing locomotion of fibroblasts, Biophys J, vol.76, pp.2307-2316, 1999.

J. De-rooij, A. Kerstens, G. Danuser, M. A. Schwartz, and C. M. Waterman­storer, Integrin­dependent actomyosin contraction regulates epithelial cell scattering, J Cell Biol, vol.171, pp.153-164, 2005.

R. P. Johnson and S. W. Craig, F­actin binding site masked by the intramolec­ ular association of vinculin head and tail domains, Nature, vol.373, pp.261-264, 1995.

R. P. Johnson and S. W. Craig, The carboxy­terminal tail domain of vinculin contains a cryptic binding site for acidic phospholipids, Biochem Bio­ phys Res Commun, vol.210, pp.159-164, 1995.

J. Jurado, J. De-navascués, and N. Gorfinkiel, alpha­Catenin stabilises cadherin­catenin complexes and modulates actomyosin dynamics to allow pulsatile apical contraction, J Cell Sci, vol.129, pp.4496-4508, 2016.

F. Kai, H. Laklai, and V. Weaver, Force matters: biomechanical regulation of cell invasion and migration in disease, Trends Cell Biol, vol.26, pp.1-12, 2016.

P. Kanchanawong, G. Shtengel, A. M. Pasapera, E. B. Ramko, M. W. Davidson et al., Nanoscale architecture of integrin­based cell adhesions, Nature, vol.468, pp.580-584, 2010.

I. Kaverina, O. Krylyshkina, K. Beningo, K. Anderson, Y. Wang et al., Tensile stress stimulates microtubule outgrowth in living cells, J Cell Sci, vol.115, pp.2283-2291, 2002.

J. P. Kerr, P. Robison, G. Shi, A. I. Bogush, A. M. Kempema et al., Detyrosinated microtubules modulate mechanotransduction in heart and skeletal muscle, Nat Com­ mun, vol.6, p.8526, 2015.

A. Kobielak and E. Fuchs, Alpha­catenin: at the junction of intercellular adhesion and actin dynamics, Nat Rev Mol Cell Biol, vol.5, pp.614-625, 2004.

M. S. Kolodney and E. L. Elson, Contraction due to microtubule disruption is associated with increased phosphorylation of myosin regulatory light chain, Proc Natl Acad Sci, vol.92, pp.10252-10256, 1995.

D. E. Koser, A. J. Thompson, S. K. Foster, A. Dwivedy, E. K. Pillai et al., Mechanosensing is critical for axon growth in the developing brain, Nat Neurosci, vol.19, pp.1592-1598, 2016.

A. Kostic, C. D. Lynch, and M. P. Sheetz, Differential matrix rigidity response in breast cancer cell lines correlates with the tissue tropism, PLoS One, vol.4, p.6361, 2009.

A. Kumar, M. Ouyang, K. Van-den-dries, E. J. Mcghee, K. Tanaka et al., Talin ten­ sion sensor reveals novel features of focal adhesion force transmission and mechanosensitivity, J Cell Biol, vol.213, pp.371-383, 2016.

A. Labernadie, T. Kato, A. Brugués, X. Serra­picamal, S. Derzsi et al., A mechanically active heterotypic E­cadherin/ N­cadherin adhesion enables fibroblasts to drive cancer cell invasion, Nat Cell Biol, vol.19, pp.224-237, 2017.

B. Ladoux, E. Anon, M. Lambert, A. Rabodzey, P. Hersen et al., Strength dependence of cadherin­mediated adhe­ sions, Biophys J, vol.98, pp.534-542, 2010.

M. Lambert, O. Thoumine, J. Brevier, D. Choquet, D. Riveline et al., Nucleation and growth of cadherin adhesions, Exp Cell Res, vol.313, pp.4025-4040, 2007.
URL : https://hal.archives-ouvertes.fr/hal-00568029

C. Lawson, S. T. Lim, S. Uryu, X. L. Chen, D. A. Calderwood et al., FAK promotes recruitment of talin to nascent adhesions to control cell motility, J Cell Biol, vol.196, pp.223-232, 2012.

D. E. Leckband and J. De-rooij, Cadherin adhesion and mechanotransduc­ tion, Annu Rev Cell Dev Biol, vol.30, pp.291-315, 2014.

C. Leduc and S. Etienne­manneville, Intermediate filaments in cell migra­ tion and invasion: the unusual suspects, Curr Opin Cell Biol, vol.32, pp.102-112, 2015.

Q. Le-duc, Q. Shi, I. Blonk, A. Sonnenberg, N. Wang et al., Vinculin potentiates E­cadherin mechanosensing and is recruited to actin­anchored sites within adherens junctions in a myosin II­depen­ dent manner, J Cell Biol, vol.189, pp.1107-1115, 2010.

E. Lee, M. L. Ewald, M. Sedarous, T. Kim, B. W. Weyers et al., Deletion of the cytoplasmic domain of N­cadherin reduces, but does not eliminate, traction force­transmission, Biochem Biophys Res Commun, vol.478, pp.1640-1646, 2016.

H. S. Lee, P. Anekal, C. J. Lim, C. C. Liu, and M. H. Ginsberg, Two modes of inte­ grin activation form a binary molecular switch in adhesion maturation, Mol Biol Cell, vol.24, pp.1354-1362, 2013.

K. R. Levental, H. Yu, L. Kass, J. N. Lakins, M. Egeblad et al., Matrix crosslinking forces tumor progression by enhancing integrin signaling, Cell, vol.139, pp.891-906, 2009.

Z. Li, H. Lee, and C. Zhu, Molecular mechanisms of mechanotransduction in integrin­mediated cell­matrix adhesion, Exp Cell Res, vol.349, pp.85-94, 2016.

C. Liu, H. Lin, M. Tang, and Y. Wang, Vimentin contributes to epithelial­ mesenchymal transition cancer cell mechanics by mediating cytoskeletal organization and focal adhesion maturation, Oncotarget, vol.6, pp.15966-15983, 2015.

Y. J. Liu, L. Berre, M. Lautenschlaeger, F. Maiuri, P. Callan­jones et al., Confinement and low adhesion induce fast amoeboid migration of slow mesenchymal cells, Cell, vol.160, pp.659-672, 2015.

M. Gupta, B. R. Sarangi, J. Deschamps, Y. Nematbakhsh, A. Callan­jones et al., Adaptive rheology and ordering of cell cytoskeleton govern matrix rigidity sens­ ing, Nat Commun, vol.6, p.7525, 2015.

A. Haining, T. J. Lieberthal, D. R. Hernández, and A. , Talin: a mechano­ sensitive molecule in health and disease, FASEB J, vol.30, pp.2073-2085, 2016.

M. Han and J. De-rooij, Converging and unique mechanisms of mecha­ notransduction at adhesion sites, Trends Cell Biol, vol.26, pp.612-623, 2016.

M. Han, E. Hoijman, E. Nöel, L. Garric, and J. Bakkers, ?E­catenin­ dependent mechanotransduction is essential for proper convergent extension in zebrafish, Biol Open, vol.5, pp.1461-1472, 2016.

A. K. Harris, P. Wild, and D. Stopak, Silicone rubber substrata: a new wrinkle in the study of cell locomotion, Science, vol.208, pp.177-179, 1980.

A. Hayer, L. Shao, M. Chung, L. Joubert, H. W. Yang et al., Engulfed cadherin fingers are polarized junc­ tional structures between collectively migrating endothelial cells, Nat Cell Biol, vol.18, pp.1311-1323, 2016.

J. N. Heck, S. M. Ponik, M. G. Garcia­mendoza, C. A. Pehlke, D. R. Inman et al., Microtubules regulate GEF­H1 in response to extracellular matrix stiffness, Mol Biol Cell, vol.23, pp.2583-2592, 2012.

H. Herrmann, H. Bär, L. Kreplak, S. V. Strelkov, and U. Aebi, Intermediate fila­ ments: from cell architecture to nanomechanics, Mol Cell Biol, vol.8, pp.562-573, 2007.

M. Himmel, A. Ritter, S. Rothemund, B. V. Pauling, K. Rottner et al., Control of high affinity interactions in the talin C ter­ minus: how talin domains coordinate protein dynamics in cell adhesions, J Biol Chem, vol.284, pp.13832-13842, 2009.

S. Hirano, N. Kimoto, Y. Shimoyama, S. Hirohashi, and M. Takeichi, Identifica­ tion of a neural alpha­catenin as a key regulator of cadherin function and multicellular organization, Cell, vol.70, pp.293-301, 1992.

E. Ho-kim, S. Song, H. , H. Yoo, S. Yoon et al., Tumor treating fields inhibit glioblastoma cell migration, invasion and angiogenesis, Oncotar­ get, vol.7, pp.65125-65136, 2016.

E. R. Horton, A. Byron, J. A. Askari, D. H. Ng, A. Millon­frémillon et al., Definition of a consensus integrin adhesome and its dynamics during adhesion com­ plex assembly and disassembly, Nat Cell Biol, vol.17, pp.1577-1587, 2015.

A. Horwitz, K. Duggan, C. Buck, M. C. Beckerle, and K. Burridge, Interaction of plasma membrane fibronectin receptor with talin-a transmembrane linkage, Nature, vol.320, pp.531-533, 1986.

X. Hu, C. Jing, X. Xu, N. Nakazawa, V. W. Cornish et al., Cooperative vinculin binding to talin mapped by time­resolved super resolution microscopy, Nano Lett, vol.16, pp.4062-4068, 2016.

J. D. Humphries, P. Wang, C. Streuli, B. Geiger, M. J. Humphries et al., Vinculin controls focal adhesion formation by direct interactions with talin and actin, J Cell Biol, vol.179, pp.1043-1057, 2007.

A. Huttenlocher and A. Horwitz, Integrins in cell migration, Cold Spring Harb Perspect Biol, vol.3, pp.47-67, 2011.

R. O. Hynes, Extracellular matrix: not just pretty fibrils, Science, vol.326, pp.1216-1219, 2009.

J. Irianto, Y. Xia, C. R. Pfeifer, A. Athirasala, J. Ji et al., DNA damage follows repair factor depletion and portends genome variation in cancer cells after article DNA damage follows repair factor depletion and portends genome variation in cancer cells after pore migration, Curr Biol, vol.27, pp.1-14, 2017.

B. C. Isenberg, P. A. Dimilla, M. Walker, S. Kim, and J. Y. Wong, Vascular smooth muscle cell durotaxis depends on substrate stiffness gradient strength, Biophys J, vol.97, pp.1313-1322, 2009.

N. Ishiyama, N. Tanaka, K. Abe, Y. J. Yang, Y. M. Abbas et al., An autoinhibited structure of ?­catenin and its implications for vinculin recruitment to adherens junctions, J Biol Chem, vol.288, pp.15913-15925, 2013.

I. L. Ivanovska, J. Shin, J. Swift, and D. E. Discher, Stem cell mechanobiol­ ogy: diverse lessons from bone marrow, Trends Cell Biol, vol.8, pp.583-592, 2015.

T. Izard and D. T. Brown, Mechanisms and functions of vinculin interactions with phospholipids at cell adhesion sites, J Biol Chem, vol.291, pp.2548-2555, 2016.

T. Izard, G. Evans, R. A. Borgon, C. L. Rush, G. Bricogne et al., Vinculin activation by talin through helical bundle conversion, Nature, vol.427, pp.171-175, 2004.

K. Jannie, S. Ellerbroek, D. Zhou, S. Chen, D. Crompton et al., Vinculin­dependent actin bundling regulates cell migration and traction forces, Biochem J, vol.465, pp.383-393, 2015.

M. Janssen, E. Kim, H. Liu, L. M. Fujimoto, A. Bobkov et al., Three­dimensional structure of vinculin bound to actin fila­ ments, Mol Cell, vol.21, pp.271-281, 2006.

R. P. Johnson and S. W. Craig, An intramolecular association between the head and tail domains of vinculin modulates talin binding, J Biol Chem, vol.269, pp.12611-12619, 1994.

M. J. Paszek, N. Zahir, K. R. Johnson, J. N. Lakins, G. I. Rozenberg et al., Tensional homeostasis and the malignant phenotype, Cancer Cell, vol.8, pp.241-254, 2005.

F. Peglion, F. Llense, and S. Etienne­manneville, Adherens junction tread­ milling during collective migration, Nat Cell Biol, vol.16, pp.639-651, 2014.

J. Pelham and Y. Wang, Cell locomotion and focal adhesions are regulated by substrate flexibility, Proc Natl Acad Sci, vol.94, pp.13661-13665, 1997.

X. Peng, E. S. Nelson, J. L. Maiers, and K. A. Demali, New insights into vinculin function and regulation, Int Rev Cell Mol Biol, vol.287, pp.191-231, 2011.

L. Petitjean, M. Reffay, E. Grasland­mongrain, M. Poujade, B. Ladoux et al., Velocity fields in a collectively migrating epithe­ lium, Biophys J, vol.98, pp.1790-1800, 2010.

S. Piccolo, S. Dupont, and M. Cordenonsi, The biology of YAP/TAZ: hippo signaling and beyond, Physiol Rev, vol.94, pp.1287-1312, 2014.

C. Plestant, P. Strale, R. Seddiki, E. Nguyen, B. Ladoux et al., Adhesive interactions of N­cadherin limit the recruitment of microtu­ bules to cell­cell contacts through organization of actomyosin, J Cell Sci, vol.127, pp.1660-1671, 2014.

S. V. Plotnikov, A. M. Pasapera, B. Sabass, and C. M. Waterman, Force fluctua­ tions within focal adhesions mediate ECM­rigidity sensing to guide directed cell migration, Cell, vol.151, pp.1513-1527, 2012.

C. Plutoni, E. Bazellieres, L. Borgne­rochet, M. Comunale, F. Brugues et al., P­cadherin promotes collective cell migration via a Cdc42­mediated increase in mechanical forces, J Cell Biol, vol.212, pp.199-217, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01878038

W. J. Polacheck and C. S. Chen, Measuring cell­generated forces: a guide to the available tools, Nat Methods, vol.13, pp.415-423, 2016.

L. Qi, N. Jafari, X. Li, Z. Chen, L. Li et al., Talin2­mediated traction force drives matrix degradation and cell invasion, J Cell Sci, vol.129, pp.3661-3674, 2016.

M. Raab and D. Discher, Matrix rigidity regulates the microtubule network polarization in migration, Cytoskeleton (Hoboken), vol.74, pp.114-124, 2016.

M. Raab, J. Swift, P. Dingal, P. Shah, J. W. Shin et al., Crawling from soft to stiff matrix polarizes the cytoskeleton and phosphoregulates myosin­II heavy chain, J Cell Biol, vol.199, pp.669-683, 2012.

A. Rape, W. Guo, and Y. Wang, Microtubule depolymerization induces traction force increase through two distinct pathways, J Cell Sci, vol.124, pp.4233-4240, 2011.

L. Rathje, N. Nordgren, T. Pettersson, D. Rönnlund, J. Widengren et al., Oncogenes induce a vimentin filament collapse mediated by HDAC6 that is linked to cell stiffness, Proc Natl Acad Sci, vol.111, pp.1515-1520, 2014.

M. Reffay, M. C. Parrini, O. Cochet­escartin, B. Ladoux, A. Buguin et al., Interplay of RhoA and mechanical forces in collective cell migration driven by leader cells, Nat Cell Biol, vol.16, pp.217-223, 2014.
URL : https://hal.archives-ouvertes.fr/hal-00992150

S. Rhee, H. Jiang, C. Ho, and F. Grinnell, Microtubule function in fibroblast spreading is modulated according to the tension state of cell­ matrix interactions, Proc Natl Acad Sci, vol.104, pp.5425-5430, 2007.

M. Riaz, M. Versaevel, D. Mohammed, K. Glinel, and S. Gabriele, Persistence of fan­shaped keratocytes is a matrix­rigidity­dependent mechanism that requires ?5?1 integrin engagement, Sci Rep, vol.6, p.34141, 2016.

D. Riveline, E. Zamir, N. Q. Balaban, U. S. Schwarz, T. Ishizaki et al., Focal contacts as mechanosen­ sors: externally applied local mechanical force induces growth of focal contacts by an mDia1­dependent and ROCK­independent mechanism, J Cell Biol, vol.153, pp.1175-1185, 2001.

P. Roca­cusachs, R. Sunyer, and X. Trepat, Mechanical guidance of cell migration: lessons from chemotaxis, Curr Opin Cell Biol, vol.25, pp.543-549, 2013.

A. Saez, A. Buguin, P. Silberzan, and B. Ladoux, Is the mechanical activity of epithelial cells controlled by deformations or forces?, Biophys J, vol.89, pp.52-54, 2005.
URL : https://hal.archives-ouvertes.fr/hal-00188263

Y. Sakamoto, B. Boeda, and S. Etienne­manneville, APC binds intermediate filaments and is required for their reorganization during cell migration, J Cell Biol, vol.200, pp.249-258, 2013.

B. R. Sarangi, M. Gupta, B. L. Doss, N. Tissot, F. Lam et al., Coordination between intra­ and extracellular forces regulates focal adhesion dynamics, Nano Lett, vol.17, pp.399-406, 2016.

R. M. Saunders, M. R. Holt, L. Jennings, D. H. Sutton, I. L. Barsukov et al., Role of vin­ culin in regulating focal adhesion turnover, Eur J Cell Biol, vol.85, pp.487-500, 2006.

Y. Sawada, M. Tamada, B. J. Dubin­thaler, O. Cherniavskaya, R. Sakai et al., Force sensing by mechanical extension of the Src family kinase substrate p130Cas, Cell, vol.127, pp.1015-1026, 2006.

Z. Liu, P. Bun, N. Audugé, M. Coppey­moisan, and N. Borghi, Vinculin head­ tail interaction defines multiple early mechanisms for stem cell rigidity sensing, Integr Biol, vol.8, pp.693-703, 2016.

Z. Liu, J. L. Tan, D. M. Cohen, M. T. Yang, N. J. Sniadecki et al., Mechanical tugging force regulates the size of cell­cell junctions, Proc Natl Acad Sci, vol.107, pp.9944-9949, 2010.

C. Lo, H. Wang, M. Dembo, and Y. Wang, Cell movement is guided by the rigidity of the substrate, Biophys J, vol.79, pp.144-152, 2000.

A. P. Maartens, J. Wellmann, E. Wictome, B. Klapholz, H. Green et al., Drosophila vinculin is more harmful when hyperactive than absent, and can circumvent integrin to form adhesion complexes, J Cell Sci, vol.129, pp.4354-4365, 2016.

P. Maiuri, J. F. Rupprecht, S. Wieser, V. Ruprecht, O. Bénichou et al., Actin flows mediate a universal coupling between cell speed and cell persistence, Cell, vol.161, pp.374-386, 2015.

K. Maki, S. Han, Y. Hirano, S. Yonemura, T. Hakoshima et al., Mechano­adaptive sensory mechanism of ?­catenin under tension, Sci Rep, vol.6, 2016.

M. Marsden and D. W. Desimone, Integrin­ECM interactions regulate cadherin­dependent cell adhesion and are required for convergent extension in Xenopus, Curr Biol, vol.13, pp.1182-1191, 2003.

V. Maruthamuthu, B. Sabass, U. S. Schwarz, and M. L. Gardel, Cell­ECM trac­ tion force modulates endogenous tension at cell­cell contacts, Proc Natl Acad Sci, vol.108, pp.4708-4713, 2011.

R. Mayor and S. Etienne­manneville, The front and rear of collective cell migration, Nat Rev Mol Cell Biol, vol.17, pp.97-109, 2016.
URL : https://hal.archives-ouvertes.fr/pasteur-02059080

H. T. Mcmahon and E. Boucrot, Membrane curvature at a glance, J Cell Sci, vol.128, pp.1065-1070, 2015.

G. Meacci, H. Wolfenson, S. Liu, M. R. Stachowiak, T. Iskratsch et al., ?­actinin links ECM rigidity sensing contractile units with periodic cell edge, Mol Biol Cell, vol.27, pp.3471-3479, 2016.

M. G. Mendez, S. Kojima, and R. D. Goldman, Vimentin induces changes in cell shape, motility, and adhesion during the epithelial to mesenchymal transition, FASEB J, vol.24, pp.1838-1851, 2010.

C. T. Mierke, P. Kollmannsberger, D. P. Zitterbart, J. Smith, B. Fabry et al., Mechano­coupling and regulation of contractility by the vinculin tail domain, Biophys J, vol.94, pp.661-670, 2008.

T. Mitchison and M. Kirschner, Cytoskeletal dynamics and nerve growth, Neuron, vol.1, pp.761-772, 1988.

D. Mitrossilis, J. Fouchard, D. Pereira, F. Postic, A. Richert et al., Real­time single­cell response to stiffness, Proc Natl Acad Sci, vol.107, pp.16518-16523, 2010.

I. Muhamed, J. Wu, P. Sehgal, X. Kong, A. Tajik et al., E­cadherin­mediated force transduction signals regulate global cell mechanics, J Cell Sci, vol.129, pp.1843-1854, 2016.

K. L. Mui, C. S. Chen, and R. K. Assoian, The mechanical regulation of integrin­ cadherin crosstalk organizes cells, signaling and forces, J Cell Sci, vol.129, pp.1093-1100, 2016.

M. E. Murray, M. G. Mendez, and P. A. Janmey, Substrate stiffness regulates solubility of cellular vimentin, Mol Biol Cell, vol.25, pp.87-94, 2014.

K. A. Myers, K. T. Applegate, G. Danuser, R. S. Fischer, and C. M. Waterman, Distinct ECM mechanosensing pathways regulate microtubule dynamics to control endothelial cell branching morphogenesis, J Cell Biol, vol.192, pp.321-334, 2011.

K. Nam, P. Kim, D. K. Wood, S. Kwon, P. P. Provenzano et al., , 2016.

, Microstructured extracellular matrices in tissue engineering and development, Curr Opin Biotechnol, vol.17, pp.518-523, 2006.

M. R. Ng, A. Besser, J. S. Brugge, and G. Danuser, Mapping the dynamics of force transduction at cell­cell junctions of epithelial clusters, Elife, vol.3, pp.1-29, 2014.

M. R. Ng, A. Besser, G. Danuser, and J. S. Brugge, Substrate stiffness regulates cadherin­dependent collective migration through myosin­II contractility, J Cell Biol, vol.199, pp.545-563, 2012.

P. Nordenfelt, H. L. Elliott, and T. A. Springer, Coordinated integrin activation by actin­dependent force during T­cell migration, Nat Commun, vol.7, p.13119, 2016.

J. Notbohm, S. Banerjee, K. Utuje, B. Gweon, H. Jang et al., Cellular contraction and polariza­ tion drive collective cellular motion, Biophys J, vol.110, pp.2729-2738, 2016.

J. Oldenburg, G. Van-der-krogt, F. Twiss, A. Bongaarts, Y. Habani et al., VASP, zyxin and TES are tension­dependent members of focal adherens junctions independent of the ?­catenin­vinculin module, Sci Rep, vol.5, p.17225, 2015.

T. M. Olson, S. Illenberger, N. Y. Kishimoto, S. Huttelmaier, and M. T. Keating, Metavinculin mutations alter actin interaction in dilated cardiomyopathy, Jock­ usch BM, vol.105, pp.431-437, 2002.

Q. Tseng, E. Duchemin­pelletier, A. Deshiere, M. Balland, H. Guillou et al., Spatial organization of the extracellular matrix regulates cell­cell junction positioning, Proc Natl Acad Sci, vol.109, pp.1506-1511, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00673247

F. Twiss, L. Duc, Q. Van-der-horst, S. Tabdili, H. Van-der-krogt et al., Vinculin­de­ pendent cadherin mechanosensing regulates efficient epithelial barrier formation, Biol Open, vol.1, pp.1128-1140, 2012.

L. Valon, A. Marín­llauradó, T. Wyatt, G. Charras, and X. Trepat, Optogenetic control of cellular forces and mechanotransduction, Nat Commun, vol.8, 2017.

V. Vasioukhin, C. Bauer, M. Yin, and E. Fuchs, Directed actin polymerization is the driving force for epithelial cell­cell adhesion, Cell, vol.100, pp.209-219, 2000.

S. Vedula, M. C. Leong, T. L. Lai, P. Hersen, A. J. Kabla et al., Emerging modes of collective cell migration induced by geo­ metrical constraints, Proc Natl Acad Sci, vol.109, pp.12974-12979, 2012.

T. Vicsek, A. Czirok, E. Ben­jacob, I. I. Cohen, and O. Schochet, Novel type of phase transition in a system of self­driven particles, Phys Rev Lett, vol.75, pp.1226-1229, 1995.

R. Vincent, E. Bazellières, C. Pérez­gonzález, M. Uroz, X. Serra­picamal et al., Active tensile modulus of an epithelial monolayer, Phys Rev Lett, vol.115, pp.1-5, 2015.

X. Wang and T. Ha, Defining single molecular forces required to activate integrin and notch signaling, Science, vol.340, pp.991-994, 2013.

X. Wang, J. Sun, Q. Xu, F. Chowdhury, M. Roein­peikar et al., Integrin molecular tension within motile focal adhesions, Biophys J, vol.109, pp.2259-2267, 2015.

Y. Wang, J. G. Miao, H. Li, J. Usami, S. Chien et al., Integrins regulate VE­cadherin and catenins: dependence of this regulation on Src, but not on Ras, Proc Natl Acad Sci, vol.103, pp.1774-1779, 2006.

G. F. Weber, M. A. Bjerke, and D. W. Desimone, Integrins and cadherins join forces to form adhesive networks, J Cell Sci, vol.124, pp.1183-1193, 2011.

G. F. Weber, M. A. Bjerke, and D. W. Desimone, A mechanoresponsive cadherin­keratin complex directs polarized protrusive behavior and col­ lective cell migration, Dev Cell, vol.22, pp.104-115, 2012.

H. Wolfenson, G. Meacci, S. Liu, M. R. Stachowiak, T. Iskratsch et al., Tropo­ myosin controls sarcomere­like contractions for rigidity sensing and suppressing growth on soft matrices, Nat Cell Biol, vol.18, pp.33-42, 2015.

W. Xu and H. Baribault, Vinculin knockout results in heart and brain de­ fects during embryonic development, Development, vol.125, pp.327-337, 1998.

H. Yamashita, T. Ichikawa, D. Matsuyama, Y. Kimura, K. Ueda et al., The role of the interaction of the vinculin proline­rich linker region with vinexin ? in sensing the stiffness of the extracellular matrix, J Cell Sci, vol.127, pp.1875-1886, 2014.

J. Yan, M. Yao, B. T. Goult, and M. P. Sheetz, Talin dependent mechanosensi­ tivity of cell focal adhesions, Cell Mol Bioeng, vol.8, pp.151-159, 2015.

B. Yang, Z. Z. Lieu, H. Wolfenson, F. M. Hameed, A. D. Bershadsky et al., Mechanosensing controlled directly by tyrosine kinases, Nano Lett, vol.16, pp.5951-5961, 2016.

M. Yao, B. T. Goult, B. Klapholz, X. Hu, C. P. Toseland et al., The mechanical response of talin, Nat Commun, vol.7, p.11966, 2016.

M. Yao, W. Qiu, R. Liu, A. K. Efremov, P. Cong et al., Force­dependent conformational switch of ?­catenin controls vinculin binding, Nat Commun, vol.5, p.4525, 2014.

X. Ye, M. A. Mclean, and S. G. Sligar, Phosphatidylinositol 4,5­bisphosphate modulates the affinity of talin­1 for phospholipid bilayers and activates its autoinhibited form, Biochemistry, vol.55, pp.5038-5048, 2016.

S. Yokoyama, T. S. Matsui, and S. Deguchi, New wrinkling substrate assay reveals traction force fields of leader and follower cells undergoing col­ lective migration, Biochem Biophys Res Commun, vol.482, pp.975-979, 2016.

S. Yonemura, Y. Wada, T. Watanabe, A. Nagafuchi, and M. Shibata, alpha­ Catenin as a tension transducer that induces adherens junction develop­ ment, Nat Cell Biol, vol.12, pp.533-542, 2010.

C. H. Yu, N. B. Rafiq, F. Cao, Y. Zhou, A. Krishnasamy et al., Integrin­beta3 clusters recruit clathrin­mediated endocytic machinery in the absence of traction force, Nat Commun, vol.6, p.8672, 2015.

R. Zaidel­bar, S. Itzkovitz, A. Ma'ayan, R. Iyengar, and B. Geiger, Functional atlas of the integrin adhesome, Nat Cell Biol, vol.9, pp.858-867, 2007.

A. Zaritsky, E. S. Welf, Y. Y. Tseng, A. Rabadan, M. Serra­picamal et al., Seeds of locally aligned motion and stress coordi­ nate a collective cell migration, Biophys J, vol.109, pp.2492-2500, 2015.

X. Zhang, G. Jiang, Y. Cai, S. J. Monkley, D. R. Critchley et al., Talin depletion reveals independence of initial cell spreading from integrin activation and traction, Nat Cell Biol, vol.10, pp.1062-1068, 2008.

J. Zimmermann, B. A. Camley, W. Rappel, and H. Levine, Contact inhibition of locomotion determines cell­cell and cell­substrate forces in tissues, Proc Natl Acad Sci, vol.113, pp.2660-2665, 2016.

E. Scarpa, . Szabo´aszabo´a, A. Bibonne, E. Theveneau, M. Parsons et al., Cadherin switch during EMT in neural crest cells leads to contact inhibi­ tion of locomotion via repolarization of forces, Dev Cell, vol.34, pp.421-434, 2015.

H. B. Schiller, M. R. Hermann, J. Polleux, T. Vignaud, S. Zanivan et al., beta1­ and alphav­ class integrins cooperate to regulate myosin II during rigidity sensing of fibronectin­based microenvironments, Nat Cell Biol, vol.15, pp.625-636, 2013.

U. S. Schwarz and M. L. Gardel, United we stand-integrating the actin cytoskeleton and cell­matrix adhesions in cellular mechanotransduction, J Cell Sci, vol.125, pp.3051-3060, 2012.

X. Serra­picamal, V. Conte, R. Vincent, E. Anon, D. T. Tambe et al., Mechanical waves during tissue expansion, Nat Phys, vol.8, pp.628-634, 2012.

P. O. Strale, L. Duchesne, G. Peyret, L. Montel, T. Nguyen et al., The formation of ordered nanoclusters controls cadherin anchoring to actin and cell­cell contact fluidity, J Cell Biol, vol.210, pp.333-346, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01313752

Z. Sun, S. S. Guo, and R. Fässler, Integrin­mediated mechanotransduction, J Cell Biol, vol.215, pp.445-456, 2016.

Z. Sun, H. Y. Tseng, S. Tan, F. Senger, L. Kurzawa et al., Kank2 activates talin, reduces force transduction across integrins and induces central adhesion forma­ tion, Nat Cell Biol, vol.18, pp.941-953, 2016.

R. Sunyer, V. Conte, J. Escribano, A. Elosegui­artola, A. Labernadie et al., Collective cell durotaxis emerges from long­range intercellular force transmission, Science, vol.353, pp.1157-1161, 2016.

V. Swaminathan and C. M. Waterman, The molecular clutch model for mechanotransduction evolves, Nat Cell Biol, vol.18, pp.459-461, 2016.

J. Swift and D. E. Discher, The nuclear lamina is mechano­responsive to ECM elasticity in mature tissue, J Cell Sci, vol.127, pp.3005-3015, 2014.

J. Swift, I. L. Ivanovska, A. Buxboim, T. Harada, P. C. Dingal et al., Nuclear lamin­A scales with tissue stiffness and enhances matrix­directed differentiation, p.1240104, 2013.

B. Szabo, G. J. Szollosi, B. Gonci, Z. Juranyi, D. Selmeczi et al., Phase transition in the collective migration of tissue cells: experiment and model, Phys Rev E Stat Nonlin Soft Matter Phys, vol.74, p.61908, 2006.

M. Takahashi, T. Ishida, O. Traub, M. A. Corson, and B. C. Berk, Mechanotrans­ duction in endothelial cells: temporal signaling events in response to shear stress, J Vasc Res, vol.34, pp.212-219, 1997.

D. T. Tambe, C. C. Hardin, T. E. Angelini, K. Rajendran, C. Y. Park et al., Collective cell guidance by cooperative intercellular forces, Nat Mater, vol.10, pp.469-475, 2011.

E. Theveneau, B. Steventon, E. Scarpa, S. Garcia, X. Trepat et al., Chase­and­run between adjacent cell populations promotes directional collective migration, Nat Cell Biol, vol.15, pp.763-772, 2013.

I. Thievessen, P. M. Thompson, S. Berlemont, K. M. Plevock, S. V. Plotnikov et al., , 2013.

, Vinculin­actin interaction couples actin retrograde flow to focal adhesions, but is dispensable for focal adhesion growth, J Cell Biol, vol.202, pp.163-177

W. A. Thomas, C. Boscher, Y. S. Chu, D. Cuvelier, C. Martinez­rico et al., alpha­Catenin and vinculin cooperate to promote high E­cadherin­based adhesion strength, J Biol Chem, vol.288, pp.4957-4969, 2013.

P. M. Thompson, S. Ramachandran, L. B. Case, C. E. Tolbert, A. Tandon et al., A structural model for vinculin insertion into PIP2­containing membranes and the effect of insertion on vinculin activation and localization, Structure, vol.25, pp.1-12, 2017.

P. M. Thompson, C. E. Tolbert, K. Shen, P. Kota, S. M. Palmer et al., Identification of an actin binding surface on vinculin that mediates mechanical cell and focal adhesion properties, Structure, vol.22, pp.697-706, 2014.

M. Tozluo?lu, A. L. Tournier, R. P. Jenkins, S. Hooper, P. A. Bates et al., Matrix geometry determines optimal cancer cell migration strategy and modulates response to interventions, Nat Cell Biol, vol.15, pp.1-14, 2013.

X. Trepat and J. J. Fredberg, Plithotaxis and emergent dynamics in collec­ tive cellular migration, Trends Cell Biol, vol.21, pp.638-646, 2011.

X. Trepat, M. R. Wasserman, T. E. Angelini, E. Millet, D. A. Weitz et al., Physical forces during collective cell migration, Nat Phys, vol.5, pp.426-430, 2009.

L. Trichet, L. Digabel, J. Hawkins, R. J. Vedula, S. Gupta et al., Evidence of a large­scale mecha­ nosensing mechanism for cellular adaptation to substrate stiffness, Proc Natl Acad Sci, vol.109, pp.6933-6938, 2012.

J. R. Tse and A. J. Engler, Stiffness gradients mimicking in vivo tissue varia­ tion regulate mesenchymal stem cell fate, PLoS One, vol.6, 2011.