Abstract
Mechanical forces play critical roles in the function of living cells. However, the underlying mechanisms of how forces influence nuclear events remain elusive. Here, we show that chromatin deformation as well as force-induced transcription of a green fluorescent protein (GFP)-tagged bacterial-chromosome dihydrofolate reductase (DHFR) transgene can be visualized in a living cell by using three-dimensional magnetic twisting cytometry to apply local stresses on the cell surface via an Arg-Gly-Asp-coated magnetic bead. Chromatin stretching depended on loading direction. DHFR transcription upregulation was sensitive to load direction and proportional to the magnitude of chromatin stretching. Disrupting filamentous actin or inhibiting actomyosin contraction abrogated or attenuated force-induced DHFR transcription, whereas activating endogenous contraction upregulated force-induced DHFR transcription. Our findings suggest that local stresses applied to integrins propagate from the tensed actin cytoskeleton to the LINC complex and then through lamina–chromatin interactions to directly stretch chromatin and upregulate transcription.
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Loops, topologically associating domains, compartments, and territories are elastic and robust to dramatic nuclear volume swelling
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Change history
27 September 2016
In the version of this Article originally published the image in Fig. 1e was incorrect. This has been corrected in all versions of the Article.
References
Discher, D. E., Mooney, D. J. & Zandstra, P. W. Growth factors, matrices, and forces combine and control stem cells. Science 324, 1673–1677 (2009).
Vogel, V. & Sheetz, M. Local force and geometry sensing regulate cell functions. Nature Rev. Mol. Cell Biol. 7, 265–275 (2006).
Friedland, J. C., Lee, M. H. & Boettiger, D. Mechanically activated integrin switch controls α5β1 function. Science 323, 642–644 (2009).
del Rio, A. et al. Stretching single talin rod molecules activates vinculin binding. Science 323, 638–641 (2009).
Grashoff, C. et al. Measuring mechanical tension across vinculin reveals regulation of focal adhesion dynamics. Nature 466, 263–266 (2010).
Austen, K. et al. Extracellular rigidity sensing by talin isoform-specific mechanical linkages. Nature Cell Biol. 17, 1597–1606 (2015).
Dupont, S. et al. Role of YAP/TAZ in mechanotransduction. Nature 474, 179–183 (2011).
Na, S. et al. Rapid signal transduction in living cells is a unique feature of mechanotransduction. Proc. Natl Acad. Sci. USA 105, 6626–6631 (2008).
Poh, Y. C. et al. Rapid activation of Rac GTPase in living cells by force is independent of Src. PLoS ONE 4, e7886 (2009).
Ouyang, M., Sun, J., Chien, S. & Wang, Y. Determination of hierarchical relationship of Src and Rac at subcellular locations with FRET biosensors. Proc. Natl Acad. Sci. USA 105, 14353–14358 (2008).
Poh, Y. C. et al. Dynamic force-induced direct dissociation of protein complexes in a nuclear body in living cells. Nature Commun. 3, 866–875 (2012).
Maniotis, A. J., Chen, C. S. & Ingber, D. E. Demonstration of mechanical connections between integrins, cytoskeletal filaments, and nucleoplasm that stabilize nuclear structure. Proc. Natl Acad. Sci. USA 94, 849–854 (1997).
Hu, S., Chen, J., Butler, J. P. & Wang, N. Prestress mediates force propagation into the nucleus. Biochem. Biophys. Res. Commun. 329, 423–428 (2005).
Lammerding, J. et al. Lamins A and C but not lamin B1 regulate nuclear mechanics. J. Biol. Chem. 281, 25768–25780 (2006).
Pajerowski, J. D., Dahl, K. N., Zhong, F. L., Sammak, P. J. & Discher, D. E. Physical plasticity of the nucleus in stem cell differentiation. Proc. Natl Acad. Sci. USA 104, 15619–15624 (2007).
Lee, J. S. et al. Nuclear lamin A/C deficiency induces defects in cell mechanics, polarization, and migration. Biophys. J. 93, 2542–2552 (2007).
Swift, J. et al. Nuclear lamin-A scales with tissue stiffness and enhances matrix-directed differentiation. Science 341, 1240104 (2013).
Ho, C. Y., Jaalouk, D. E., Vartiainen, M. K. & Lammerding, J. Lamin A/C and emerin regulate MKL1-SRF activity by modulating actin dynamics. Nature 497, 507–511 (2013).
Jain, N., Iyer, K. V., Kumar, A. & Shivashankar, G. V. Cell geometric constraints induce modular gene-expression patterns via redistribution of HDAC3 regulated by actomyosin contractility. Proc. Natl Acad. Sci. USA 110, 11349–11354 (2013).
Guilluy, C. et al. Isolated nuclei adapt to force and reveal a mechanotransduction pathway in the nucleus. Nature Cell Biol. 16, 376–381 (2014).
Poirier, M. G., Eroglu, S. & Marko, J. F. The bending rigidity of mitotic chromosomes. Mol. Biol. Cell 13, 2170–2179 (2002).
Houchmandzadeh, B., Marko, J. F., Chatenay, D. & Libchaber, A. Elasticity and structure of eukaryote chromosomes studied by micromanipulation and micropipette aspiration. J. Cell Biol. 139, 1–12 (1997).
Carpenter, A. E., Memedula, S., Plutz, M. J. & Belmont, A. S. Common effects of acidic activators on large-scale chromatin structure and transcription. Mol. Cell. Biol. 25, 958–968 (2005).
Chuang, C. H. et al. Long-range directional movement of an interphase chromosome site. Curr. Biol. 16, 825–831 (2006).
Therizols, P. et al. Chromatin decondensation is sufficient to alter nuclear organization in embryonic stem cells. Science 346, 1238–1242 (2014).
Hu, Y., Kireev, I., Plutz, M., Ashourian, N. & Belmont, A. S. Large-scale chromatin structure of inducible genes: transcription on a condensed, linear template. J. Cell Biol. 185, 87–100 (2009).
Hu, S. et al. Mechanical anisotropy of adherent cells probed by a three dimensional magnetic twisting device. Am. J. Physiol. Cell Physiol. 287, C1184–C1191 (2004).
Sinclair, P., Bian, Q., M.Plutz, M., Heard, E. & Belmont, A. S. Dynamic plasticity of large-scale chromatin structure revealed by self-assembly of engineered chromosome regions. J. Cell Biol. 190, 761–776 (2010).
Wang, N., Tytell, J. D. & Ingber, D. E. Mechanotransduction at a distance: mechanically coupling the extracellular matrix with the nucleus. Nature Rev. Mol. Cell Biol. 10, 75–82 (2009).
Tan, Y. et al. Matrix softness regulates plasticity of tumour-repopulating cells via H3K9 demethylation and Sox2 expression. Nature Commun. 5, 4619 (2014).
Engler, A. J., Sen, S., Sweeney, H. L. & Discher, D. E. Matrix elasticity directs stem cell lineage specification. Cell 126, 677–689 (2006).
Liu, J. et al. Soft fibrin gels promote selection and growth of tumorigenic cells. Nature Mater. 11, 734–741 (2012).
Dingal, P. C. & Discher, D. E. Systems mechanobiology: tension-inhibited protein turnover is sufficient to physically control gene circuits. Biophys. J. 107, 2734–2743 (2014).
Schwachtgen, J. L., Houston, P., Campbell, C., Sukhatme, V. & Braddock, M. Fluid shear stress activation of egr-1 transcription in cultured human endothelial and epithelial cells is mediated via the extracellular signal-related kinase 1/2 mitogen-activated protein kinase pathway. J. Clin. Invest. 101, 2540–2549 (1998).
Legant, W. R. et al. Multidimensional traction force microscopy reveals out-of-plane rotational moments about focal adhesions. Proc. Natl Acad. Sci. USA 110, 881–886 (2013).
Acknowledgements
This work was supported by NIH R01 GM072744 (to N.W.) NIH R01 GM58460 (to A.S.B.), and funds from Huazhong University of Science and Technology, and Ministry of Science and Technology of China grant 2016YFA0101100. A.T. acknowledges partial support from Natural Sciences and Engineering Research Council (NSERC) of Canada through a PGS Doctoral Scholarship. R.S. acknowledges support from the NSF IGERT Program. N.W. acknowledges support from a Hoeft Professorship at University of Illinois at Urbana-Champaign.
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N.W. and A.S.B. conceived the project. N.W., A.S.B., A.T., Y.Z., F.W. and J.S. designed the project. A.T., Y.Z., F.W., J.S., Q.J., W.Z., R.S. and N.K. performed experiments and analyses. N.W., A.T., F.W., J.S. and A.S.B. wrote the manuscript with inputs from all other authors.
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Tajik, A., Zhang, Y., Wei, F. et al. Transcription upregulation via force-induced direct stretching of chromatin. Nature Mater 15, 1287–1296 (2016). https://doi.org/10.1038/nmat4729
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DOI: https://doi.org/10.1038/nmat4729
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