Appreciating force and shape—the rise of mechanotransduction in cell biology
Open accessAbstract
Although the shapes of organisms are encoded in their genome, the developmental processes that lead to the final form of vertebrates involve a constant feedback between dynamic mechanical forces, and cell growth and motility. Mechanobiology has emerged as a discipline dedicated to the study of the effects of mechanical forces and geometry on cell growth and motility—for example, during cell-matrix adhesion development—through the signalling process of mechanotransduction.
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Cells such as macrophages actively interact with their mechanical environment and modulate their inflammatory activity in response.
“Cells such as macrophages are known to actively interact with their mechanical environment and modulate their inflammatory activity in response (Iskratsch et al., 2014).”
From Foreign Body Reaction to Implanted Biomaterials and Its Impact in Nerve Neuroprosthetics (2021) · cites this paper as Iskratsch et al., 2014
The Abstract describes cells dynamically interacting with mechanical aspects of their microenvironment, and Future perspective and conclusions says cells actively test that environment and respond to it. Neither passage establishes the claim specifically for macrophages or says that mechanical cues modulate their inflammatory activity. (LLM, conf=0.85)
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Cites
Calcium's Role in Mechanotransduction during Muscle Development
Damm, T. B., & Egli, M. (2014) · Cellular Physiology and Biochemistry · doi:10.1159/000356667 · Cited by 14,548 · see citing works
Matrix elasticity directs stem cell lineage specification
Engler, A. J., Sen, S., Sweeney, H. L., & Discher, D. E. (2006) · Cell · doi:10.1016/j.cell.2006.06.044 · Cited by 13,915 · see citing works
Role of YAP/TAZ in mechanotransduction
Dupont, S., Morsut, L., Aragona, M., Enzo, E., Giulitti, S., Cordenonsi, M., Zanconato, F., Le Digabel, J., Forcato, M., Bicciato, S., et al. (2011) · Nature · doi:10.1038/nature10137 · Cited by 5,979 · see citing works
The heat of shortening and the dynamic constants of muscle
Hill, A. V. (1938) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1938.0050 · Cited by 5,570 · see citing works
Geometric Control of Cell Life and Death
Chen, C. S., Mrksich, M., Huang, S., Whitesides, G. M., & Ingber, D. E. (1997) · Science · doi:10.1126/science.276.5317.1425 · Cited by 4,628 · see citing works
Cellular Motility Driven by Assembly and Disassembly of Actin Filaments
Pollard, T. D., & Borisy, G. G. (2003) · Cell · doi:10.1016/s0092-8674(03)00120-x · Cited by 4,203 · see citing works
Thompson, D. W. (2019) · Princeton University Press eBooks · doi:10.1515/9780691183978-018 · Cited by 4,179 · see citing works
Cell locomotion and focal adhesions are regulated by substrate flexibility.
Pelham, R., & Wang, Y.-L. (1997) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.94.25.13661 · Cited by 3,156 · see citing works
Reversible Unfolding of Individual Titin Immunoglobulin Domains by AFM
Rief, M., Gautel, M., Oesterhelt, F., Fernández, J. M., & Gaub, H. E. (1997) · Science · doi:10.1126/science.276.5315.1109 · Cited by 3,081 · see citing works
Mechanotransduction Across the Cell Surface and Through the Cytoskeleton
Wang, N., Butler, J. P., & Ingber, D. E. (1993) · Science · doi:10.1126/science.7684161 · Cited by 3,007 · see citing works
Regulatory networks defining EMT during cancer initiation and progression
Craene, B. D., & Berx, G. (2013) · Nature Reviews Cancer · doi:10.1038/nrc3447 · Cited by 2,487 · see citing works
Balaban, N. Q., Schwarz, U. S., Riveline, D., Goichberg, P., Tzur, G., Sabanay, I., Mahalu, D., Safran, S. A., Bershadsky, A. D., Addadi, L., et al. (2001) · Nature Cell Biology · doi:10.1038/35074532 · Cited by 2,137 · see citing works
Cells lying on a bed of microneedles: An approach to isolate mechanical force
Tan, J. L., Tien, J., Pirone, D. M., Gray, D. S., Bhadriraju, K., & Chen, C. S. (2003) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.0235407100 · Cited by 2,036 · see citing works
The Mechanism of Muscular Contraction
Huxley, H. E. (1969) · Science · doi:10.1126/science.164.3886.1356 · Cited by 1,974 · see citing works
Thompson, D. W. (1917) · University Press eBooks · doi:10.5962/bhl.title.11332 · Cited by 1,923 · see citing works
Huxley, H. E., & Hanson, J. (1954) · Nature · doi:10.1038/173973a0 · Cited by 1,755 · see citing works
Energy landscapes of receptor–ligand bonds explored with dynamic force spectroscopy
Merkel, R., Nassoy, P., Leung, A., Ritchie, K. P., & Evans, E. A. (1999) · Nature · doi:10.1038/16219 · Cited by 1,724 · see citing works
Aragona, M., Panciera, T., Manfrin, A., Giulitti, S., Michielin, F., Elvassore, N., Dupont, S., & Piccolo, S. (2013) · Cell · doi:10.1016/j.cell.2013.07.042 · Cited by 1,651 · see citing works
Structural Changes in Muscle During Contraction: Interference Microscopy of Living Muscle Fibres
HUXLEY, A. F., & NIEDERGERKE, R. (1954) · Nature · doi:10.1038/173971a0 · Cited by 1,608 · see citing works
Measuring mechanical tension across vinculin reveals regulation of focal adhesion dynamics
Grashoff, C., Hoffman, B. D., Brenner, M. D., Zhou, R., Parsons, M., Yang, M. T., McLean, M. A., Sligar, S. G., Chen, C. S., Ha, T., et al. (2010) · Nature · doi:10.1038/nature09198 · Cited by 1,549 · see citing works
Stretching Single Talin Rod Molecules Activates Vinculin Binding
Hernández, A. E. D. R., Pérez‐Jiménez, R., Liu, R., Roca‐Cusachs, P., Fernández, J. M., & Sheetz, M. P. (2009) · Science · doi:10.1126/science.1162912 · Cited by 1,509 · see citing works
Self-citationEngineering cell shape and function
Singhvi, R., Kumar, A., Lopez, G. P., Stephanopoulos, G. N., Wang, D. I. C., Whitesides, G. M., & Ingber, D. E. (1994) · Science · doi:10.1126/science.8171320 · Cited by 1,453 · see citing works
Focal Contacts as Mechanosensors
Riveline, D., Zamir, E., Balaban, N. Q., Schwarz, U. S., Ishizaki, T., Narumiya, S., Kam, Z., Geiger, B., & Bershadsky, A. D. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.153.6.1175 · Cited by 1,421 · see citing works
Biological Membranes as Bilayer Couples. A Molecular Mechanism of Drug-Erythrocyte Interactions
Sheetz, M. P., & Singer, S. J. (1974) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.71.11.4457 · Cited by 1,389 · see citing works
Self-citationSilicone Rubber Substrata: A New Wrinkle in the Study of Cell Locomotion
Harris, A. K., Wild, P., & Stopak, D. (1980) · Science · doi:10.1126/science.6987736 · Cited by 1,348 · see citing works
Extracellular Matrix Rigidity Causes Strengthening of Integrin–Cytoskeleton Linkages
Choquet, D., Felsenfeld, D. P., & Sheetz, M. P. (1997) · Cell · doi:10.1016/s0092-8674(00)81856-5 · Cited by 1,248 · see citing works
Self-citationNelson, C. M., & Bissell, M. J. (2006) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.22.010305.104315 · Cited by 1,121 · see citing works
Haemodynamic shear stress activates a K+ current in vascular endothelial cells
Olesen, S., Clapham, D. E., & Davies, P. F. (1988) · Nature · doi:10.1038/331168a0 · Cited by 1,002 · see citing works
The locomotion of fibroblasts in culture
Abercrombie, M., Heaysman, J. E. M., & Pegrum, S. M. (1971) · Experimental Cell Research · doi:10.1016/0014-4827(71)90420-4 · Cited by 970 · see citing works
A Nucleator Arms Race: Cellular Control of Actin Assembly
Campellone, K. G., & Welch, M. D. (2010) · Nature reviews. Molecular cell biology · doi:10.1038/nrm2867 · Cited by 959 · see citing works
Force Sensing by Mechanical Extension of the Src Family Kinase Substrate p130Cas
Sawada, Y., Tamada, M., Dubin‐Thaler, B. J., Cherniavskaya, O., Sakai, R., Tanaka, S., & Sheetz, M. P. (2006) · Cell · doi:10.1016/j.cell.2006.09.044 · Cited by 945 · see citing works
Self-citationTraction Dynamics of Filopodia on Compliant Substrates
Chan, C. E., & Odde, D. J. (2008) · Science · doi:10.1126/science.1163595 · Cited by 942 · see citing works
Stress fibers are generated by two distinct actin assembly mechanisms in motile cells
Hotulainen, P., & Lappalainen, P. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200511093 · Cited by 941 · see citing works
The relationship between force and focal complex development
Galbraith, C. G., Yamada, K. M., & Sheetz, M. P. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200204153 · Cited by 908 · see citing works
Self-citationIntermolecular Forces and Energies Between Ligands and Receptors
Moy, V. T., Florin, E., & Gaub, H. E. (1994) · Science · doi:10.1126/science.7939660 · Cited by 878 · see citing works
Plotnikov, S. V., Pasapera, A. M., Sabass, B., & Waterman, C. M. (2012) · Cell · doi:10.1016/j.cell.2012.11.034 · Cited by 866 · see citing works
Knöll, R., Hoshijima, M., Hoffman, H. M., Person, V., Lorenzen-Schmidt, I., Bang, M.-L., Hayashi, T., Shiga, N., Yasukawa, H., Schaper, W., et al. (2002) · Cell · doi:10.1016/s0092-8674(02)01226-6 · Cited by 786 · see citing works
Izzard, C. S., & Lochner, L. R. (1976) · Journal of Cell Science · doi:10.1242/jcs.21.1.129 · Cited by 711 · see citing works
On the mechanical factors which determine the output of the ventricles
Patterson, S. W., & Starling, E. H. (1914) · The Journal of Physiology · doi:10.1113/jphysiol.1914.sp001669 · Cited by 641 · see citing works
α-Actinin: Immunofluorescent localization of a muscle structural protein in nonmuscle cells
Lazarides, E., & Burridge, K. (1975) · Cell · doi:10.1016/0092-8674(75)90180-4 · Cited by 609 · see citing works
THE MECHANISM OF ADHESION OF CELLS TO GLASS
Curtis, A. S. G. (1964) · The Journal of Cell Biology · doi:10.1083/jcb.20.2.199 · Cited by 594 · see citing works
The Kinase Domain of Titin Controls Muscle Gene Expression and Protein Turnover
Lange, S., Xiang, F., Yakovenko, A. R., Vihola, A., Hackman, P., Rostkova, E. V., Kristensen, J., Brandmeier, B., Franzen, G., Hedberg, B., et al. (2005) · Science · doi:10.1126/science.1110463 · Cited by 594 · see citing works
Periodic Lamellipodial Contractions Correlate with Rearward Actin Waves
Giannone, G., Dubin‐Thaler, B. J., Döbereiner, J., Kieffer, N., Bresnick, A. R., & Sheetz, M. P. (2004) · Cell · doi:10.1016/s0092-8674(04)00058-3 · Cited by 584 · see citing works
Self-citationPrager‐Khoutorsky, M., Lichtenstein, A., Krishnan, R., Rajendran, K., Mayo, A., Kam, Z., Geiger, B., & Bershadsky, A. D. (2011) · Nature Cell Biology · doi:10.1038/ncb2370 · Cited by 564 · see citing works
IRSp53 is an essential intermediate between Rac and WAVE in the regulation of membrane ruffling
Miki, H., Yamaguchi, H., Suetsugu, S., & Takenawa, T. (2000) · Nature · doi:10.1038/35047107 · Cited by 557 · see citing works
Characteristics of an assay for Rous sarcoma virus and Rous sarcoma cells in tissue culture
Temin, H. M., & Rubin, H. (1958) · Virology · doi:10.1016/0042-6822(58)90114-4 · Cited by 554 · see citing works
Src kinase activation by direct interaction with the integrin β cytoplasmic domain
Arias‐Salgado, E. G., Lizano, S., Sarkar, S., Brugge, J. S., Ginsberg, M. H., & Shattil, S. J. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2336149100 · Cited by 554 · see citing works
The regulation of the heart beat
Patterson, S. W., Piper, H., & Starling, E. H. (1914) · The Journal of Physiology · doi:10.1113/jphysiol.1914.sp001676 · Cited by 549 · see citing works
Differential Transmission of Actin Motion Within Focal Adhesions
Hu, K., Ji, L., Applegate, K. T., Danuser, G. M., & Waterman, C. M. (2007) · Science · doi:10.1126/science.1135085 · Cited by 512 · see citing works
A micromachined device provides a new bend on fibroblast traction forces.
Galbraith, C., & Sheetz, M. (1997) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.94.17.9114 · Cited by 436 · see citing works
Self-citationThe Molecular Basis of Filamin Binding to Integrins and Competition with Talin
Kiema, T., Lad, Y., Jiang, P., Oxley, C. L., Baldassarre, M., Wegener, K. L., Campbell, I. D., Ylänne, J., & Calderwood, D. A. (2006) · Molecular Cell · doi:10.1016/j.molcel.2006.01.011 · Cited by 434 · see citing works
Cooperative effects of Rho and mechanical stretch on stress fiber organization
Kaunas, R. R., Nguyen, P., Usami, S., & Chien, S. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506041102 · Cited by 418 · see citing works
Heath, J. P., & Dunn, G. (1978) · Journal of Cell Science · doi:10.1242/jcs.29.1.197 · Cited by 415 · see citing works
Thoumine, O. R., & Ott, A. (1997) · Journal of Cell Science · doi:10.1242/jcs.110.17.2109 · Cited by 412 · see citing works
Gauthier, N. C., Fardin, M.-A., Roca‐Cusachs, P., & Sheetz, M. P. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1105845108 · Cited by 396 · see citing works
Self-citationKNOWLTON, F. P., & Starling, E. H. (1912) · The Journal of Physiology · doi:10.1113/jphysiol.1912.sp001511 · Cited by 393 · see citing works
Carisey, A. F., Tsang, R., Greiner, A. M., Nijenhuis, N., Heath, N., Nazgiewicz, A., Kemkemer, R., Derby, B., Spatz, J. P., & Ballestrem, C. (2013) · Current Biology · doi:10.1016/j.cub.2013.01.009 · Cited by 374 · see citing works
Schwarz, U. S., Balaban, N. Q., Riveline, D., et al. (2002) · Biophysical Journal · doi:10.1016/s0006-3495(02)73909-x · Cited by 371 · see citing works
Nuclear Actin Network Assembly by Formins Regulates the SRF Coactivator MAL
Baarlink, C., Wang, H., & Grosse, R. (2013) · Science · doi:10.1126/science.1235038 · Cited by 351 · see citing works
The switchable integrin adhesome
Zaidel‐Bar, R., & Geiger, B. (2010) · Journal of Cell Science · doi:10.1242/jcs.066183 · Cited by 350 · see citing works
Mechanoenzymatics of titin kinase
Puchner, E. M., Alexandrovich, A., Kho, A. L., Hensen, U., Schäfer, L. V., Brandmeier, B., Gräter, F., Grubmüller, H., Gaub, H. E., & Gautel, M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0805034105 · Cited by 347 · see citing works
Schiller, H. B., Friedel, C. C., Boulègue, C., & Fässler, R. (2011) · EMBO Reports · doi:10.1038/embor.2011.5 · Cited by 346 · see citing works
The myosin swinging cross-bridge model
Spudich, J. A. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35073086 · Cited by 341 · see citing works
Costameres, focal adhesions, and cardiomyocyte mechanotransduction
Samarel, A. M. (2005) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00749.2005 · Cited by 300 · see citing works
Focal adhesions as mechanosensors: A physical mechanism
Shemesh, T., Geiger, B., Bershadsky, A. D., & Kozlov, M. M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0500254102 · Cited by 299 · see citing works
Puklin-Faucher, E., & Sheetz, M. P. (2008) · Journal of Cell Science · doi:10.1242/jcs.042127 · Cited by 295 · see citing works
Self-citationForce transduction by Triton cytoskeletons
Sawada, Y., & Sheetz, M. P. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200110068 · Cited by 290 · see citing works
Self-citationRoca‐Cusachs, P., Hernández, A. E. D. R., Puklin-Faucher, E., Gauthier, N. C., Biais, N., & Sheetz, M. P. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1220723110 · Cited by 287 · see citing works
Self-citationCells test substrate rigidity by local contractions on submicrometer pillars
Ghassemi, S., Meacci, G., Liu, S., Gondarenko, A. A., Mathur, A., Roca‐Cusachs, P., Sheetz, M. P., & Hone, J. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1119886109 · Cited by 276 · see citing works
Self-citationGiannone, G., Jiang, G., Sutton, D. H., Critchley, D. R., & Sheetz, M. P. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200302001 · Cited by 276 · see citing works
Self-citationSubstrate rigidity and force define form through tyrosine phosphatase and kinase pathways
Giannone, G., & Sheetz, M. P. (2006) · Trends in Cell Biology · doi:10.1016/j.tcb.2006.02.005 · Cited by 271 · see citing works
Self-citationBuckley, M. J., Banes, A. J., Levin, L. G., Sumpio, B. E., Sato, M., Jordan, R., Gilbert, J. L., Link, G. W., & Tay, R. T. S. (1988) · PubMed · Cited by 269 · see citing works
Neidlinger‐Wilke, C., Wilke, H., & Claes, L. (1994) · Journal of Orthopaedic Research® · doi:10.1002/jor.1100120109 · Cited by 259 · see citing works
Finding the weakest link – exploring integrin-mediated mechanical molecular pathways
Roca‐Cusachs, P., Iskratsch, T., & Sheetz, M. P. (2012) · Journal of Cell Science · doi:10.1242/jcs.095794 · Cited by 258 · see citing works
Self-citationBeil, M., Micoulet, A., von Wichert, G., Paschke, S., Walther, P., Omary, M. B., Veldhoven, P. P. V., Gern, U., Wolf-Hieber, E., Eggermann, J., et al. (2003) · Nature Cell Biology · doi:10.1038/ncb1037 · Cited by 254 · see citing works
Visualizing mechanical tension across membrane receptors with a fluorescent sensor
Stabley, D. R., Jurchenko, C., Marshall, S., & Salaita, K. S. (2011) · Nature Methods · doi:10.1038/nmeth.1747 · Cited by 248 · see citing works
Jungbauer, S., Gao, H., Spatz, J. P., & Kemkemer, R. (2008) · Biophysical Journal · doi:10.1529/biophysj.107.128611 · Cited by 247 · see citing works
Franck, C., Hong, S. S., Maskarinec, S. A., et al. (2007) · Experimental Mechanics · doi:10.1007/s11340-007-9037-9 · Cited by 239 · see citing works
Rigidity Sensing at the Leading Edge through αvβ3 Integrins and RPTPα
Jiang, G., Huang, A., Cai, Y., Tanase, M., & Sheetz, M. P. (2005) · Biophysical Journal · doi:10.1529/biophysj.105.072462 · Cited by 234 · see citing works
Self-citationKolega, J. J. (1986) · The Journal of Cell Biology · doi:10.1083/jcb.102.4.1400 · Cited by 231 · see citing works
Formin mDia1 senses and generates mechanical forces on actin filaments
Jegou, A. G., Carlier, M., & Romet‐Lemonne, G. (2013) · Nature Communications · doi:10.1038/ncomms2888 · Cited by 222 · see citing works
Mechanotransduction In Vivo by Repeated Talin Stretch-Relaxation Events Depends upon Vinculin
Margadant, F., Chew, L. L., Hu, X., Yu, H., Bate, N., Zhang, X., & Sheetz, M. (2011) · PLoS Biology · doi:10.1371/journal.pbio.1001223 · Cited by 215 · see citing works
Self-citationThe emergence of integrins: a personal and historical perspective
Hynes, R. O. (2004) · Matrix Biology · doi:10.1016/j.matbio.2004.08.001 · Cited by 209 · see citing works
Traction forces in locomoting cells
Oliver, T., Jacobson, K., & Dembo, M. (1995) · Cell Motility and the Cytoskeleton · doi:10.1002/cm.970310306 · Cited by 207 · see citing works
Purification and properties of native titin
Trinick, J. A., Knight, P. J., & Whiting, A. H. (1984) · Journal of Molecular Biology · doi:10.1016/s0022-2836(84)80007-8 · Cited by 206 · see citing works
Yu, C., Law, J. B. K., Suryana, M., Low, H. Y., & Sheetz, M. P. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1109485108 · Cited by 205 · see citing works
Self-citationRPTP-α acts as a transducer of mechanical force on αv/β3-integrin–cytoskeleton linkages
von Wichert, G., Jiang, G., Kostić, A., Vos, K. J. D., Sap, J., & Sheetz, M. P. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200211061 · Cited by 204 · see citing works
Self-citationInvolvement of extracellular matrix constituents in breast cancer
Lochter, A., & Bissell, M. J. (1995) · Seminars in Cancer Biology · doi:10.1006/scbi.1995.0017 · Cited by 198 · see citing works
Cytoskeletal coherence requires myosin-IIA contractility
Cai, Y., Rossier, O., Gauthier, N. C., Biais, N., Fardin, M.-A., Zhang, X., Miller, L. W., Ladoux, B., Cornish, V. W., & Sheetz, M. P. (2010) · Journal of Cell Science · doi:10.1242/jcs.058297 · Cited by 192 · see citing works
Self-citationHayakawa, K., Sato, N., & Obinata, T. (2001) · Experimental Cell Research · doi:10.1006/excr.2001.5270 · Cited by 186 · see citing works
Burridge, K., & Connell, L. B. (1983) · Cell Motility · doi:10.1002/cm.970030509 · Cited by 176 · see citing works
Xu, Y., Bismar, T. A., Su, J., Xu, B., Kristiansen, G., Varga, Z., Teng, L., Ingber, D. E., Mammoto, A., Kumar, R., et al. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20100433 · Cited by 174 · see citing works
Cell locomotion, nerve elongation, and microfilaments
Ludueña, M. A., & Wessells, N. K. (1973) · Developmental Biology · doi:10.1016/0012-1606(73)90100-0 · Cited by 171 · see citing works
A fluorescence energy transfer‐based mechanical stress sensor for specific proteins in situ
Meng, F., Suchyna, T. M., & Sachs, F. (2008) · FEBS Journal · doi:10.1111/j.1742-4658.2008.06461.x · Cited by 167 · see citing works
Dynamic force sensing of filamin revealed in single-molecule experiments
Rognoni, L., Stigler, J., Pelz, B., Ylänne, J., & Rief, M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1211274109 · Cited by 159 · see citing works
FAK Potentiates Rac1 Activation and Localization to Matrix Adhesion Sites: A Role for βPIX
Chang, F., Lemmon, C. A., Park, D., et al. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-03-0207 · Cited by 156 · see citing works
The mechanism of muscular contraction. Science 164:1356-1366, 1969.
Huxley, H. E. (2002) · PubMed · Cited by 153 · see citing works
Brown, A. C., Fiore, V. F., Sulchek, T., & Barker, T. H. (2012) · The Journal of Pathology · doi:10.1002/path.4114 · Cited by 148 · see citing works
Tension modulates actin filament polymerization mediated by formin and profilin
Courtemanche, N., Lee, J. Y., Pollard, T. D., & Greene, E. C. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1308257110 · Cited by 138 · see citing works
Tension Sensing Nanoparticles for Mechano-Imaging at the Living/Nonliving Interface
Liu, Y., Yehl, K. M., Narui, Y., et al. (2013) · Journal of the American Chemical Society · doi:10.1021/ja401494e · Cited by 136 · see citing works
Liu, W. F., Nelson, C. M., Tan, J. L., & Chen, C. S. (2007) · Circulation Research · doi:10.1161/circresaha.107.158329 · Cited by 133 · see citing works
Dubin‐Thaler, B. J., Hofman, J. M., Cai, Y., Xenias, H. S., Spielman, I., Shneidman, A. V., David, L. A., Döbereiner, J., Wiggins, C. H., & Sheetz, M. P. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003735 · Cited by 127 · see citing works
Self-citationTransient Frictional Slip between Integrin and the ECM in Focal Adhesions under Myosin II Tension
Aratyn-Schaus, Y., & Gardel, M. L. (2010) · Current Biology · doi:10.1016/j.cub.2010.05.049 · Cited by 122 · see citing works
Processive capping by formin suggests a force-driven mechanism of actin polymerization
Kozlov, M. M., & Bershadsky, A. D. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200410017 · Cited by 120 · see citing works
Fibronectin Rigidity Response through Fyn and p130Cas Recruitment to the Leading Edge
Kostić, A., & Sheetz, M. P. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e05-12-1161 · Cited by 119 · see citing works
Self-citationSanford, K. K., Likely, G. D., & Earle, W. R. (1954) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/15.2.215 · Cited by 117 · see citing works
Zhao, R., Boudou, T., Wang, W., Chen, C. S., & Reich, D. H. (2013) · Advanced Materials · doi:10.1002/adma.201203585 · Cited by 107 · see citing works
Goldyn, A. M., Rioja, B. A., Spatz, J. P., Ballestrem, C., & Kemkemer, R. (2009) · Journal of Cell Science · doi:10.1242/jcs.054866 · Cited by 107 · see citing works
Limitation of Cell Adhesion by the Elasticity of the Extracellular Matrix
Nicolas, A., & Safran, S. A. (2006) · Biophysical Journal · doi:10.1529/biophysj.105.077115 · Cited by 107 · see citing works
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Iskratsch, T., Yu, C., Mathur, A., et al. (2013) · Developmental Cell · doi:10.1016/j.devcel.2013.11.003 · Cited by 105 · see citing works
Self-citationOn the constancy of the systolic output under varying conditions
Markwalder, J., & Starling, E. H. (1914) · The Journal of Physiology · doi:10.1113/jphysiol.1914.sp001668 · Cited by 93 · see citing works
O’Connor, J. W., & Gomez, E. W. (2013) · PLoS ONE · doi:10.1371/journal.pone.0083188 · Cited by 91 · see citing works
Coussen, F., Choquet, D., Sheetz, M. P., & Erickson, H. (2002) · Journal of Cell Science · doi:10.1242/jcs.115.12.2581 · Cited by 88 · see citing works
Self-citationIntegrin-Generated Forces Lead to Streptavidin-Biotin Unbinding in Cellular Adhesions
Jurchenko, C., Chang, Y., Narui, Y., et al. (2014) · Biophysical Journal · doi:10.1016/j.bpj.2014.01.049 · Cited by 83 · see citing works
Theory of Force Regulation by Nascent Adhesion Sites
Bruinsma, R. (2005) · Biophysical Journal · doi:10.1529/biophysj.104.048280 · Cited by 83 · see citing works
A Physicist's Renewed Look at Biology: Twenty Years Later
Delbrück, M. (1970) · Science · doi:10.1126/science.168.3937.1312 · Cited by 68 · see citing works
Rahmouni, S., Lindner, A., Rechenmacher, F., Neubauer, S., Sobahi, T. R., Kessler, H., Cavalcanti‐Adam, E. A., & Spatz, J. P. (2013) · Advanced Materials · doi:10.1002/adma.201301338 · Cited by 64 · see citing works
The integrin β tail is required and sufficient to regulate adhesion signaling to Rac1
Berrier, A. L., Martinez, R. J., Bokoch, G., et al. (2002) · Journal of Cell Science · doi:10.1242/jcs.00109 · Cited by 64 · see citing works
FHOD1 regulates stress fiber organization by controlling transversal arc and dorsal fiber dynamics
Schulze, N., Graessl, M., Soares, A. B., Geyer, M., Dehmelt, L., & Nalbant, P. (2014) · Journal of Cell Science · doi:10.1242/jcs.134627 · Cited by 58 · see citing works
Mechanical Response Analysis and Power Generation by Single‐Cell Stretching
Micoulet, A., Spatz, J. P., & Ott, A. (2005) · ChemPhysChem · doi:10.1002/cphc.200400417 · Cited by 57 · see citing works
Flux at Focal Adhesions: Slippage Clutch, Mechanical Gauge, or Signal Depot
Wang, Y. (2007) · Science s STKE · doi:10.1126/stke.3772007pe10 · Cited by 52 · see citing works
The NPIY motif in the integrin β1 tail dictates the requirement for talin-1 in outside-in signaling
Nieves, B., Jones, C. W., Ward, R., Ohta, Y., Reverte, C. G., & LaFlamme, S. E. (2010) · Journal of Cell Science · doi:10.1242/jcs.056549 · Cited by 52 · see citing works
Lynch, C. D., Lazar, A. M., Iskratsch, T., et al. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-05-0377 · Cited by 47 · see citing works
Self-citationLim, C. T., Bershadsky, A. D., & Sheetz, M. P. (2010) · Journal of The Royal Society Interface · doi:10.1098/rsif.2010.0150.focus · Cited by 41 · see citing works
Self-citationEvidence for Multisite Ligand Binding and Stretching of Filamin by Integrin and Migfilin
Ithychanda, S. S., & Qin, J. (2011) · Biochemistry · doi:10.1021/bi2003229 · Cited by 30 · see citing works
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Guimarães, C. F., Gasperini, L., Marques, A. P., & Reis, R. L. (2020) · Nature Reviews Materials · doi:10.1038/s41578-019-0169-1 · Cited by 1,515 · see citing works
Targeting integrin pathways: mechanisms and advances in therapy
Pang, X., He, X., Qiu, Z., Zhang, H., Xie, R., Liu, Z., Gu, Y., Zhao, N., Xiang, Q., & Cui, Y. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01259-6 · Cited by 1,275 · see citing works
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“Cells such as macrophages are known to actively interact with theirmechanical environment and modulate their inflammatory activity in response (Iskratsch et al., 2014).”
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“281 Consequently, treatments targeting the mechanical TME represent an emerging strategy in targeted therapy.”
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Su, J., Song, Y., Zhu, Z., Huang, X., Fan, J., Qiao, J., & Mao, F. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01888-z · Cited by 433 · see citing works
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Wackerhage, H., Schoenfeld, B. J., Hamilton, D. L., Lehti, M., & Hulmi, J. J. (2019) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00685.2018 · Cited by 357 · see citing works
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Goult, B. T., Yan, J., & Schwartz, M. A. (2018) · Journal of Cell Biology · doi:10.1083/jcb.201808061 · Cited by 250 · see citing works
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Friston, K., Levin, M., Sengupta, B., & Pezzulo, G. (2015) · Journal of The Royal Society Interface · doi:10.1098/rsif.2014.1383 · Cited by 234 · see citing works
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Emon, B., Bauer, J., Jain, Y., Jung, B., & Saif, T. (2018) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2018.07.003 · Cited by 245 · see citing works
Jain, N., Moeller, J., & Vogel, V. (2019) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-062117-121224 · Cited by 237 · see citing works
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Herrmann, M., Engelke, K., Ebert, R., Müller-Deubert, S., Rudert, M., Ziouti, F., Jundt, F., Felsenberg, D., & Jakob, F. (2020) · Biomolecules · doi:10.3390/biom10030432 · Cited by 197 · see citing works
Carnicer-Lombarte (2019) · doi:10.1101/829648 · Cited by 46 · see citing works
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- Authors
- Iskratsch, T., Wolfenson, H., & Sheetz, M. P.
- Affiliations
- Columbia University (US)
- National University of Singapore (SG)
- Corresponding author
- Sheetz, Michael P.
- Venue
- Nature Reviews Molecular Cell Biology
- Published
- 2014-10-30
- Volume
- 15
- Issue
- 12
- Pages
- 825-833
- ISSN
- 1471-0072 (ISSN-L)
- 1471-0080
- PMC
- PMC9339222
- OpenAlex
- W1970570245
- Cited by
- 798
- References
- 125
- Citations by year
- 2026: 46 · 2025: 61 · 2024: 76 · 2023: 73 · 2022: 90 · 2021: 80 · 2020: 77 · 2019: 71 · 2018: 73 · 2017: 62 · 2016: 48 · 2015: 39 · 2014: 2
- FWCI
- 5.05
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Molecular Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Research Portal (King's College London) (submittedVersion)
- Funders
- National Institute of Biomedical Imaging and Bioengineering (R01EB001480)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Hippo pathway signaling and YAP/TAZ
- Physical Sciences › Physics and Astronomy › Atomic and Molecular Physics, and Optics › Force Microscopy Techniques and Applications
- Keywords
- mechanotransduction, mechanobiology, mechanical forces, cell shape, cell growth, cell motility, cell-matrix adhesion, developmental forms, geometry
- MeSH terms
- Animals, Biomechanical Phenomena, Cell Biology, Extracellular Matrix, Mechanotransduction, Cellular, History, 20th Century, History, 21st Century
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