P. A. Janmey, R. G. Wells, R. K. Assoian, and C. A. Mcculloch, From tissue mechanics to transcription factors, Differentiation, vol.86, p.23969122, 2013.

T. Iba and B. E. Sumpio, Morphological response of human endothelial cells subjected to cyclic strain in vitro, Microvascular Research, vol.42, p.1779881, 1991.

S. Li, M. P. Czubryt, J. Mcanally, R. Bassel-duby, J. A. Richardson et al., Requirement for serum response factor for skeletal muscle growth and maturation revealed by tissue-specific gene deletion in mice, Proceedings of the National Academy of Sciences, vol.102, p.15647354, 2005.

R. Jano?tiak, A. C. Pataki, and J. Brábek, Rö sel D. Mechanosensors in integrin signaling: The emerging role of p130Cas, European Journal of Cell Biology, vol.93, p.25062607, 2014.

L. Blanchoin, R. Boujemaa-paterski, C. Sykes, and J. Plastino, Actin Dynamics, Architecture, and Mechanics in Cell Motility, Physiological Reviews, vol.94, p.24382887, 2014.
URL : https://hal.archives-ouvertes.fr/hal-00943523

T. Morita, T. Mayanagi, and K. Sobue, Reorganization of the actin cytoskeleton via transcriptional regulation of cytoskeletal/focal adhesion genes by myocardin-related transcription factors

, Experimental Cell Research, vol.313, p.17714703, 2007.

W. W. Ahmed, T. Wolfram, A. M. Goldyn, K. Bruellhoff, B. A. Rioja et al., Myoblast morphology and organization on biochemically micro-patterned hydrogel coatings under cyclic mechanical strain, Biomaterials, vol.31, p.19783042, 2010.

M. G. Mendez and P. A. Janmey, Transcription factor regulation by mechanical stress. The International Journal of, Biochemistry & Cell Biology, vol.44, p.22387568, 2012.

A. Sotiropoulos, D. Gineitis, J. Copeland, and R. Treisman, Signal-Regulated Activation of Serum Response Factor Is Mediated by Changes in Actin Dynamics, Cell, vol.98, issue.00, p.10428028, 1999.

D. Wang, S. Li, D. Hockemeyer, L. Sutherland, Z. Wang et al., Potentiation of serum response factor activity by a family of myocardin-related transcription factors, Proceedings of the National Academy of Sciences, vol.99, p.12397177, 2002.

B. Cen, A. Selvaraj, R. C. Burgess, J. K. Hitzler, Z. Ma et al., Megakaryoblastic Leukemia 1, a Potent Transcriptional Coactivator for Serum Response Factor (SRF), Is Required for Serum Induction of SRF Target Genes, Molecular and Cellular Biology, vol.23, p.12944485, 2003.

K. Kalita, G. Kharebava, J. Zheng, and M. Hetman, Role of Megakaryoblastic Acute Leukemia-1 in ERK1/2-Dependent Stimulation of Serum Response Factor-Driven Transcription by BDNF or Increased Synaptic Activity, Journal of Neuroscience, vol.26, p.17005865, 2006.

K. Kalita, B. Kuzniewska, and L. Kaczmarek, MKLs: Co-factors of serum response factor (SRF) in neuronal responses, The International Journal of Biochemistry & Cell Biology, vol.44, p.22626970, 2012.

A. Gerber, C. Esnault, A. G. Treisman, R. Pralong, F. Schibler et al., Blood-Borne Circadian Signal Stimulates Daily Oscillations in Actin Dynamics and SRF Activity, Cell, vol.152, p.23374345, 2013.

E. W. Gomez, Q. K. Chen, N. Gjorevski, and C. M. Nelson, Tissue geometry patterns epithelial-mesenchymal transition via intercellular mechanotransduction, Journal of Cellular Biochemistry, p.20336666, 2010.

J. T. Connelly, J. E. Gautrot, B. Trappmann, D. Tan, G. Donati et al., Actin and serum response factor transduce physical cues from the microenvironment to regulate epidermal stem cell fate decisions, Nature Cell Biology, vol.12, p.20581838, 2010.

A. Selvaraj and R. Prywes, Megakaryoblastic Leukemia-1/2, a Transcriptional Co-activator of Serum Response Factor, Is Required for Skeletal Myogenic Differentiation, J Biol Chem, vol.278, p.14565952, 2003.

V. Randrianarison-huetz, A. Papaefthymiou, G. Herledan, C. Noviello, U. Faradova et al., Srf controls satellite cell fusion through the maintenance of actin architecture, The Journal of Cell Biology, vol.217, p.29269426, 2018.

C. Esnault, A. Stewart, F. Gualdrini, P. East, S. Horswell et al., Rho-actin signaling to the MRTF coactivators dominates the immediate transcriptional response to serum in fibroblasts, Genes & Development, vol.28, p.24732378, 2014.

A. Guerci, C. Lahoute, S. Hébrard, L. Collard, D. Graindorge et al., Srf-Dependent Paracrine Signals Produced by Myofibers Control Satellite Cell-Mediated Skeletal Muscle Hypertrophy, Cell Metabolism, vol.15, p.22225874, 2012.

L. Collard, G. Herledan, A. Pincini, A. Guerci, V. Randrianarison-huetz et al., Nuclear actin and myocardin-related transcription factors control disuse muscle atrophy through regulation of Srf activity, Journal of Cell Science, vol.127, p.25344251, 2014.

F. Miralles, G. Posern, A. Zaromytidou, and R. Treisman, Actin dynamics control SRF activity by regulation of its coactivator MAL, Cell, pp.329-342, 2003.

M. K. Vartiainen, S. Guettler, B. Larijani, and R. Treisman, Nuclear Actin Regulates Dynamic Subcellular Localization and Activity of the SRF Cofactor MAL, Science, vol.316, p.17588931, 2007.

S. Mouilleron, S. Guettler, C. A. Langer, R. Treisman, and N. Q. Mcdonald, Molecular basis for G-actin binding to RPEL motifs from the serum response factor coactivator MAL, The EMBO Journal, vol.27, p.19008859, 2008.

S. Guettler, M. K. Vartiainen, F. Miralles, B. Larijani, and R. Treisman, RPEL Motifs Link the Serum Response Factor Cofactor MAL but Not Myocardin to Rho Signaling via Actin Binding, Mol Cell Biol, vol.28, p.18025109, 2008.

H. Hirano and Y. Matsuura, Sensing actin dynamics: Structural basis for G-actin-sensitive nuclear import of MAL, Biochemical and Biophysical Research Communications, vol.414, p.21964294, 2011.

R. Paw?owski, E. K. Rajakylä, M. K. Vartiainen, and R. Treisman, An actin-regulated importin ?/?-dependent extended bipartite NLS directs nuclear import of MRTF-A, The EMBO Journal, vol.29, p.20818336, 2010.

C. Baarlink, H. Wang, and R. Grosse, Nuclear Actin Network Assembly by Formins Regulates the SRF Coactivator MAL, Science, vol.340, p.23558171, 2013.

M. R. Lundquist, A. J. Storaska, T. Liu, S. D. Larsen, T. Evans et al., Redox Modification of Nuclear Actin by MICAL-2 Regulates SRF Signaling, Cell, vol.156, p.24440334, 2014.

M. A. Scharenberg, B. E. Pippenger, R. Sack, D. Zingg, J. Ferralli et al., TGF-induced differentiation into myofibroblasts involves specific regulation of two MKL1 isoforms, Journal of Cell Science, vol.127, p.24424023, 2014.

X. Zhao, C. Laschinger, P. Arora, K. Szaszi, A. Kapus et al., Force activates smooth muscle -actin promoter activity through the Rho signaling pathway, Journal of Cell Science, vol.120, p.17456553, 2007.

S. Albinsson, I. Nordström, and P. Hellstrand, Stretch of the Vascular Wall Induces Smooth Muscle Differentiation by Promoting Actin Polymerization, J Biol Chem, vol.279, p.15184395, 2004.

D. P. Staus, A. L. Blaker, J. M. Taylor, and C. P. Mack, Diaphanous 1 and 2 Regulate Smooth Muscle Cell Differentiation by Activating the Myocardin-Related Transcription Factors. Arteriosclerosis, Thrombosis, and Vascular Biology, vol.27, p.17170370, 2007.

K. Kuwahara, H. Kinoshita, Y. Kuwabara, Y. Nakagawa, S. Usami et al., Myocardin-Related Transcription Factor A Is a Common Mediator of Mechanical Stress-and Neurohumoral StimulationInduced Cardiac Hypertrophic Signaling Leading to Activation of Brain Natriuretic Peptide Gene Expression, Mol Cell Biol, vol.30, p.20606005, 2010.

X. Huang, N. Yang, V. F. Fiore, T. H. Barker, Y. Sun et al., Matrix Stiffness-Induced Myofibroblast Differentiation Is Mediated by Intrinsic Mechanotransduction, American Journal of Respiratory Cell and Molecular Biology, vol.47, p.22461426, 2012.

M. Chan, F. Chaudary, W. Lee, J. W. Copeland, and C. A. Mcculloch, Force-induced Myofibroblast Differentiation through Collagen Receptors Is Dependent on Mammalian Diaphanous (mDia), J Biol Chem, vol.285, pp.9273-9281, 2010.

K. V. Iyer, S. Pulford, A. Mogilner, and G. V. Shivashankar, Mechanical Activation of Cells Induces Chromatin Remodeling Preceding MKL Nuclear Transport, Biophysical Journal, vol.103, p.23062334, 2012.

P. Strale, L. Duchesne, G. Peyret, L. Montel, T. Nguyen et al., The formation of ordered nanoclusters controls cadherin anchoring to actin and cell-cell contact fluidity, The Journal of Cell Biology, vol.210, p.26195669, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01313752

E. E. Charrier, L. Montel, A. Asnacios, F. Delort, P. Vicart et al., The desmin network is a determinant of the cytoplasmic stiffness of myoblasts, Biology of the Cell, vol.110, p.29388701, 2018.

D. Icard-arcizet, O. Cardoso, and A. Richert, Hé non S. Cell Stiffening in Response to External Stress is Correlated to Actin Recruitment, Biophysical Journal, vol.94, p.18178644, 2008.

N. Courtemanche, T. D. Pollard, and Q. Chen, Avoiding artefacts when counting polymerized actin in live cells with LifeAct fused to fluorescent proteins, Nature Cell Biology, vol.18, p.27159499, 2016.

H. S. Van-der-honing, L. S. Van-bezouwen, A. Emons, and T. Ketelaar, High expression of Lifeact in Arabidopsis thaliana reduces dynamic reorganization of actin filaments but does not affect plant development, Cytoskeleton, vol.68, p.21948789, 2011.

L. P. Cramer, L. J. Briggs, and H. R. Dawe, Use of fluorescently labelled deoxyribonuclease I to spatially measure G-actin levels in migrating and non-migrating cells, Cell Motility, vol.51, p.11810694, 2002.

G. Lukinavi?ius, L. Reymond, D. 'este, E. Masharina, A. Göttfert et al., Fluorogenic probes for livecell imaging of the cytoskeleton, Nature Methods, vol.11, p.24859753, 2014.

Y. Ben-ari, Y. Brody, N. Kinor, A. Mor, T. Tsukamoto et al., The life of an mRNA in space and time, Journal of Cell Science, vol.123, p.20427315, 2010.

S. B. Khatau, C. M. Hale, P. J. Stewart-hutchinson, M. S. Patel, C. L. Stewart et al., A perinuclear actin cap regulates nuclear shape, Proceedings of the National Academy of Sciences, vol.106, pp.19017-19022, 2009.

A. B. Chambliss, S. B. Khatau, N. Erdenberger, D. K. Robinson, D. Hodzic et al., The LINCanchored actin cap connects the extracellular milieu to the nucleus for ultrafast mechanotransduction, Scientific Reports, vol.3, p.23336069, 2013.

A. Elosegui-artola, I. Andreu, A. Beedle, A. Lezamiz, M. Uroz et al., Force Triggers YAP Nuclear Entry by Regulating Transport across Nuclear Pores, Cell, vol.171, p.29107331, 2017.