• Journal of Semiconductors
  • Vol. 41, Issue 4, 041607 (2020)
Wang Xi, Delphine Delacour, and Benoit Ladoux
Author Affiliations
  • Cell Adhesion and Mechanics, Institut Jacques Monod, CNRS UMR7592, Paris Diderot University, 75205 Paris Cedex 13, France
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    DOI: 10.1088/1674-4926/41/4/041607 Cite this Article
    Wang Xi, Delphine Delacour, Benoit Ladoux. Designer substrates and devices for mechanobiology study[J]. Journal of Semiconductors, 2020, 41(4): 041607 Copy Citation Text show less
    References

    [1] W Xi, T B Saw, D Delacour et al. Material approaches to active tissue mechanics. Nat Rev Mater, 4, 23(2019).

    [2] J Prost, F Jülicher, J F Joanny. Active gel physics. Nat Phys, 11, 111(2015).

    [3] M C Marchetti, J F Joanny, S Ramaswamy et al. Hydrodynamics of soft active matter. Rev Mod Phys, 85, 1143(2013).

    [4] D Needleman, Z Dogic. Active matter at the interface between materials science and cell biology. Nat Rev Mater, 2, 17048(2017).

    [5] C Grashoff, B D Hoffman, M D Brenner et al. Measuring mechanical tension across vinculin reveals regulation of focal adhesion dynamics. Nature, 466, 263(2010).

    [6] G Giannone, B J Dubin-Thaler, H G Döbereiner et al. Periodic lamellipodial contractions correlate with rearward actin waves. Cell, 116, 431(2004).

    [7] A Ray, O Lee, Z Win et al. Anisotropic forces from spatially constrained focal adhesions mediate contact guidance directed cell migration. Nat Commun, 8, 14923(2017).

    [8] X Jiang, D A Bruzewicz, A P Wong et al. Directing cell migration with asymmetric micropatterns. Proc Natl Acad Sci USA, 102, 975(2005).

    [9] B Chen, G Kumar, C C Co et al. Geometric control of cell migration. Sci Rep, 3, 1(2013).

    [10] H E Johnson, S J King, S B Asokan et al. F-actin bundles direct the initiation and orientation of lamellipodia through adhesion-based signaling. J Cell Biol, 208, 443(2015).

    [11] A J Engler, S Sen, H L Sweeney et al. Matrix elasticity directs stem cell lineage specification. Cell, 126, 677(2006).

    [12] S R Naganathan, T C Middelkoop, S Fürthauer et al. Actomyosin-driven left-right asymmetry: from molecular torques to chiral self organization. Curr Opin Cell Biol, 38, 24(2016).

    [13] Y H Tee, T Shemesh, V Thiagarajan et al. Cellular chirality arising from the self-organization of the actin cytoskeleton. Nat Cell Biol, 17, 445(2015).

    [14] M Gupta, B R Sarangi, J Deschamps et al. Adaptive rheology and ordering of cell cytoskeleton govern matrix rigidity sensing. Nat Commun, 6, 1(2015).

    [15] L Trichet, J Le Digabel, R J Hawkins et al. Evidence of a large-scale mechanosensing mechanism for cellular adaptation to substrate stiffness. Proc Natl Acad Sci USA, 109, 6933(2012).

    [16] A Zemel, F Rehfeldt, A E Brown et al. Optimal matrix rigidity for stress-fibre polarization in stem cells. Nat Phys, 6, 468(2010).

    [17] E M Levina, L V Domnina, Y A Rovensky et al. Cylindrical substratum induces different patterns of actin microfilament bundles in nontransformed and in ras-transformed epitheliocytes. Exp Cell Res, 229, 159(1996).

    [18] T M Svitkina, Y A Rovensky, A D Bershadsky et al. Transverse pattern of microfilament bundles induced in epitheliocytes by cylindrical substrata. J Cell Sci, 108, 735(1995).

    [19] B Sun, K Xie, T H Chen et al. Preferred cell alignment along concave microgrooves. RSC Adv, 7, 6788(2017).

    [20] Y Y Biton, S A Safran. The cellular response to curvature-induced stress. Phys Biol, 6, 046010(2009).

    [21] N D Bade, R D Kamien, R K Assoian et al. Curvature and Rho activation differentially control the alignment of cells and stress fibers. Sci Adv, 3, e1700150(2017).

    [22] R De, A Zemel, S A Safran. Dynamics of cell orientation. Nat Phys, 3, 655(2007).

    [23] A Livne, E Bouchbinder, B Geiger. Cell reorientation under cyclic stretching. Nat Commun, 5, 3938(2014).

    [24] V K Sidhaye, K S Schweitzer, M J Caterina et al. Shear stress regulates aquaporin-5 and airway epithelial barrier function. Proc Natl Acad Sci USA, 105, 3345(2008).

    [25] B Ladoux, R M Mège. Mechanobiology of collective cell behaviours. Nat Rev Molecul Cell Biol, 18, 743(2017).

    [26] S Wong, W H Guo, Y L Wang. Fibroblasts probe substrate rigidity with filopodia extensions before occupying an area. Proc Natl Acad Sci USA, 111, 17176(2014).

    [27] A Saez, M Ghibaudo, A Buguin et al. Rigidity-driven growth and migration of epithelial cells on microstructured anisotropic substrates. Proc Natl Acad Sci USA, 104, 8281(2007).

    [28] X Wang, S Li, C Yan et al. Fabrication of RGD micro/nanopattern and corresponding study of stem cell differentiation. Nano Lett, 15, 1457(2015).

    [29] T B Saw, A Doostmohammadi, V Nier et al. Topological defects in epithelia govern cell death and extrusion. Nature, 544, 212(2017).

    [30] J Salomon, C Gaston, J Magescas et al. Contractile forces at tricellular contacts modulate epithelial organization and monolayer integrity. Nat Commun, 8, 13998(2017).

    [31] Y Wang, D B Gunasekara, M I Reed et al. A microengineered collagen scaffold for generating a polarized crypt-villus architecture of human small intestinal epithelium. Biomaterials, 128, 44(2017).

    [32] K M Stroka, H Jiang, S H Chen et al. Water permeation drives tumor cell migration in confined microenvironments. Cell, 157, 611(2014).

    [33] M Raab, M Gentili, H de Belly et al. ESCRT III repairs nuclear envelope ruptures during cell migration to limit DNA damage and cell death. Science, 352, 359(2016).

    [34] C M Denais, R M Gilbert, P Isermann et al. Nuclear envelope rupture and repair during cancer cell migration. Science, 352, 353(2016).

    [35] H D Moreau, C Blanch-Mercader, R Attia et al. Macropinocytosis overcomes directional bias in dendritic cells due to hydraulic resistance and facilitates space exploration. Develop Cell, 49, 171(2019).

    [36] W Xi, C K Schmidt, S Sanchez et al. Rolled-up functionalized nanomembranes as three-dimensional cavities for single cell studies. Nano Lett, 14, 4197(2014).

    [37] W Xi, C K Schmidt, S Sanchez et al. Molecular insights into division of single human cancer cells in on-chip transparent microtubes. ACS Nano, 10, 5835(2016).

    [38] B Koch, A K Meyer, L Helbig et al. Dimensionality of rolled-up nanomembranes controls neural stem cell migration mechanism. Nano Lett, 15, 5530(2015).

    [39] F X Maquart, J C Monboisse. Extracellular matrix and wound healing. Pathol Biol, 62, 91(2014).

    [40] H Kobayashi, A Enomoto, S L Woods et al. Cancer-associated fibroblasts in gastrointestinal cancer. Nat Rev Gastroenterol Hepatol, 16, 282(2019).

    [41] H K Kleinman, D Philp, M P Hoffman. Role of the extracellular matrix in morphogenesis. Curr Opin Biotechnol, 14, 526(2003).

    [42] Y Xia, G M Whitesides. Soft lithography. Ann Rev Mater Sci, 28, 153(1998).

    [43] D Qin, Y Xia, G M Whitesides. Soft lithography for micro-and nanoscale patterning. Nat Protoc, 5, 491(2010).

    [44] Y Xia, E Kim, X M Zhao et al. Complex optical surfaces formed by replica molding against elastomeric masters. Science, 273, 347(1996).

    [45] P O Strale, A Azioune, G Bugnicourt et al. Multiprotein printing by light-induced molecular adsorption. Adv Mater, 28, 2024(2016).

    [46] C S Chen, M Mrksich, S Huang et al. Geometric control of cell life and death. Science, 276, 1425(1997).

    [47] J T Parsons, A R Horwitz, M A Schwartz. Cell adhesion: integrating cytoskeletal dynamics and cellular tension. Nat Rev Mol Cell Biol, 11, 633(2010).

    [48] P Kanchanawong, G Shtengel, A M Pasapera et al. Nanoscale architecture of integrin-based cell adhesions. Nature, 468, 580(2010).

    [49] N Wang, J P Butler, D E Ingber. Mechanotransduction across the cell surface and through the cytoskeleton. Science, 260, 1124(1993).

    [50] N Q Balaban, U S Schwarz, D Riveline et al. Force and focal adhesion assembly: a close relationship studied using elastic micropatterned substrates. Nat Cell Biol, 3, 466(2001).

    [51] X Wang, T Ha. Defining single molecular forces required to activate integrin and notch signaling. Science, 340, 991(2013).

    [52] J Fink, N Carpi, T Betz et al. External forces control mitotic spindle positioning. Nat Cell Biol, 13, 771(2011).

    [53] D E Discher, P Janmey, Y L Wang. Tissue cells feel and respond to the stiffness of their substrate. Science, 310, 1139(2005).

    [54] O Du Roure, A Saez, A Buguin et al. Force mapping in epithelial cell migration. Proc Natl Acad Sci USA, 102, 2390(2005).

    [55] Y Shao, J Fu. Integrated micro/nanoengineered functional biomaterials for cell mechanics and mechanobiology: a materials perspective. Adv Mater, 26, 1494(2014).

    [56] R J Pelham, Y L Wang. Cell locomotion and focal adhesions are regulated by substrate flexibility. Proc Natl Acad Sci USA, 94, 13661(1997).

    [57] B R Sarangi, M Gupta, B L Doss et al. Coordination between intra-and extracellular forces regulates focal adhesion dynamics. Nano Lett, 17, 399(2017).

    [58] D Mitrossilis, J Fouchard, A Guiroy et al. Single-cell response to stiffness exhibits muscle-like behavior. Proc Natl Acad Sci USA, 106, 18243(2009).

    [59] R Sunyer, V Conte, J Escribano et al. Collective cell durotaxis emerges from long-range intercellular force transmission. Science, 353, 1157(2016).

    [60] M J Paszek, N Zahir, K R Johnson et al. Tensional homeostasis and the malignant phenotype. Cancer Cell, 8, 241(2005).

    [61] K R Levental, H Yu, L Kass et al. Matrix crosslinking forces tumor progression by enhancing integrin signaling. Cell, 139, 891(2009).

    [62] S M Weiz, M Medina-Sánchez, O G Schmidt. Microsystems for single-cell analysis. Adv Biosyst, 2, 1700193(2018).

    [63] M Ghibaudo, L Trichet, J Le Digabel et al. Substrate topography induces a crossover from 2D to 3D behavior in fibroblast migration. Biophys J, 97, 357(2009).

    [64] P Clark, P Connolly, A S Curtis et al. Topographical control of cell behaviour. I. Simple step cues. Development, 99, 439(1987).

    [65] E K Yim, R M Reano, S W Pang et al. Nanopattern-induced changes in morphology and motility of smooth muscle cells. Biomaterials, 26, 5405(2005).

    [66] G M Whitesides. The origins and the future of microfluidics. Nature, 442, 368(2006).

    [67] N J Douville, P Zamankhan, Y C Tung et al. Combination of fluid and solid mechanical stresses contribute to cell death and detachment in a microfluidic alveolar model. Lab Chip, 11, 609(2011).

    [68] J Rahimzadeh, F Meng, F Sachs et al. Real-time observation of flow-induced cytoskeletal stress in living cells. Am J Physiol-Cell Physiol, 301, C646(2011).

    [69] Y Imura, K Sato, E Yoshimura. Micro total bioassay system for ingested substances: assessment of intestinal absorption, hepatic metabolism, and bioactivity. Anal Chem, 82, 9983(2010).

    [70] H A Praetorius, K R Spring. Bending the MDCK cell primary cilium increases intracellular calcium. J Membr Biol, 184, 71(2001).

    [71] H A Praetorius, K R Spring. Removal of the MDCK cell primary cilium abolishes flow sensing. J Membr Biol, 191, 69(2003).

    [72] K J Jang, K Y Suh. A multi-layer microfluidic device for efficient culture and analysis of renal tubular cells. Lab Chip, 10, 36(2010).

    [73] K J Jang, H S Cho, D H Kang et al. Fluid-shear-stress-induced translocation of aquaporin-2 and reorganization of actin cytoskeleton in renal tubular epithelial cells. Integr Biol, 3, 134(2011).

    [74] K J Jang, A P Mehr, G A Hamilton et al. Human kidney proximal tubule-on-a-chip for drug transport and nephrotoxicity assessment. Integr Biol, 5, 1119(2013).

    [75] N Baeyens, C Bandyopadhyay, B G Coon et al. Endothelial fluid shear stress sensing in vascular health and disease. J Clin Invest, 126, 821(2016).

    [76] S Kawashima, M Yokoyama. Dysfunction of endothelial nitric oxide synthase and atherosclerosis. Arterioscler, Thromb, Vasc Biol, 24, 998(2004).

    [77] N Baeyens, M J Mulligan-Kehoe, F Corti et al. Syndecan 4 is required for endothelial alignment in flow and atheroprotective signaling. Proc Natl Acad Sci USA, 111, 17308(2014).

    [78] D E Conway, M T Breckenridge, E Hinde et al. Fluid shear stress on endothelial cells modulates mechanical tension across VE-cadherin and PECAM-1. Curr Biol, 23, 1024(2013).

    [79] R Jr Steward, D Tambe, C C Hardin et al. Fluid shear, intercellular stress, and endothelial cell alignment. Am J Physiol-Cell Physiol, 308, C657(2015).

    [80] S S Hur, J C Del Alamo, J S Park et al. Roles of cell confluency and fluid shear in 3-dimensional intracellular forces in endothelial cells. Proc Natl Acad Sci USA, 109, 11110(2012).

    [81] S Ohta, S Inasawa, Y Yamaguchi. Alignment of vascular endothelial cells as a collective response to shear flow. J Phys D, 48, 245401(2015).

    [82] H J Lee, M F Diaz, K M Price et al. Fluid shear stress activates YAP1 to promote cancer cell motility. Nat Commun, 8, 14122(2017).

    [83] W J Polacheck, J L Charest, R D Kamm. Interstitial flow influences direction of tumor cell migration through competing mechanisms. Proc Natl Acad Sci USA, 108, 11115(2011).

    [84] A S Piotrowski-Daspit, J Tien, C M Nelson. Interstitial fluid pressure regulates collective invasion in engineered human breast tumors via Snail, vimentin, and E-cadherin. Integr Biol, 8, 319(2016).

    [85] S N Bhatia, D E Ingber. Microfluidic organs-on-chips. Nat Biotechnol, 32, 760(2014).

    [86] L Li, J Eyckmans, C S Chen. Designer biomaterials for mechanobiology. Nat Mater, 16, 1164(2017).

    Wang Xi, Delphine Delacour, Benoit Ladoux. Designer substrates and devices for mechanobiology study[J]. Journal of Semiconductors, 2020, 41(4): 041607
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