The DOI matches its Crossref record; 71 of the 71 references it cites were found in a registry or an index.
Chromatin and lamin A determine two different mechanical response regimes of the cell nucleus
Open accessAbstract
The cell nucleus must continually resist and respond to intercellular and intracellular mechanical forces to transduce mechanical signals and maintain proper genome organization and expression. Altered nuclear mechanics is associated with many human diseases, including heart disease, progeria, and cancer. Chromatin and nuclear envelope A-type lamin proteins are known to be key nuclear mechanical components perturbed in these diseases, but their distinct mechanical contributions are not known. Here we directly establish the separate roles of chromatin and lamin A/C and show that they determine two distinct mechanical regimes via micromanipulation of single isolated nuclei. Chromatin governs response to small extensions (<3 μm), and euchromatin/heterochromatin levels modulate the stiffness. In contrast, lamin A/C levels control nuclear strain stiffening at large extensions. These results can be understood through simulations of a polymeric shell and cross-linked polymer interior. Our results provide a framework for understanding the differential effects of chromatin and lamin A/C in cell nuclear mechanics and their alterations in disease.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Computer Simulation of Liquids
Allen, M. P., & Tildesley, D. J. (2017) · doi:10.1093/oso/9780198803195.001.0001 · Cited by 20,945
Computer Simulation of Liquids
P, S., & J, K. (1988) · Journal of Molecular Liquids · doi:10.1016/0167-7322(88)80022-9 · Cited by 15,812
Comprehensive Mapping of Long-Range Interactions Reveals Folding Principles of the Human Genome
Lieberman-Aiden, E., van Berkum, N. L., Williams, L., Imakaev, M., Ragoczy, T., Telling, A., Amit, I., Lajoie, B. R., Sabo, P. J., Dorschner, M. O., et al. (2009) · Science · doi:10.1126/science.1181369 · Cited by 8,898
Nuclear Lamin-A Scales with Tissue Stiffness and Enhances Matrix-Directed Differentiation
Swift, J., Ivanovska, I. L., Buxboim, A., Harada, T., Dingal, P. C. D. P., Pinter, J., Pajerowski, J. D., Spinler, K. R., Shin, J.-W., Tewari, M., et al. (2013) · Science · doi:10.1126/science.1240104 · Cited by 1,991
Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions
Guelen, L., Pagie, L., Brasset, E., Meuleman, W., Faza, M. B., Talhout, W., Eussen, B. H., de Klein, A., Wessels, L., de Laat, W., et al. (2008) · Nature · doi:10.1038/nature06947 · Cited by 1,953
Yoshida, M., Kijima, M., Akita, M., & Beppu, T. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)44885-x · Cited by 1,854
An oestrogen-receptor-α-bound human chromatin interactome
Fullwood, M. J., Liu, M. H., Pan, Y. F., Liu, J., Xu, H., Mohamed, Y. B., Orlov, Y. L., Velkov, S., Ho, A., Mei, P. H., et al. (2009) · Nature · doi:10.1038/nature08497 · Cited by 1,721
Wolf, K., te Lindert, M., Krause, M., Alexander, S., te Riet, J., Willis, A. L., Hoffman, R. M., Figdor, C. G., Weiss, S. J., & Friedl, P. (2013) · Journal of Cell Biology · doi:10.1083/jcb.201210152 · Cited by 1,375
Nuclear envelope rupture and repair during cancer cell migration
Denais, C. M., Gilbert, R. M., Isermann, P., McGregor, A. L., te Lindert, M., Weigelin, B., Davidson, P. M., Friedl, P., Wolf, K., & Lammerding, J. (2016) · Science · doi:10.1126/science.aad7297 · Cited by 1,318
Loss of a-Type Lamin Expression Compromises Nuclear Envelope Integrity Leading to Muscular Dystrophy
Sullivan, T., Escalante-Alcalde, D., Bhatt, H., Anver, M., Bhat, N., Nagashima, K., Stewart, C. L., & Burke, B. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.147.5.913 · Cited by 1,211
Lamin A-dependent nuclear defects in human aging
Scaffidi, P., & Misteli, T. (2006) · Science · doi:10.1126/science.1127168 · Cited by 1,125
Goldman, R. D., Shumaker, D. K., Erdos, M. R., Eriksson, M., Goldman, A. E., Gordon, L. B., Gruenbaum, Y., Khuon, S., Mendez, M., Varga, R., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402943101 · Cited by 1,103
Self-citationMendez, M. G., Kojima, S., & Goldman, R. D. (2010) · The FASEB Journal · doi:10.1096/fj.09-151639 · Cited by 939
Self-citationPhysical plasticity of the nucleus in stem cell differentiation
Pajerowski, J. D., Dahl, K. N., Zhong, F. L., Sammak, P. J., & Discher, D. E. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0702576104 · Cited by 833
Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging
Shumaker, D. K., Dechat, T., Kohlmaier, A., Adam, S. A., Bozovsky, M. R., Erdos, M. R., Eriksson, M., Goldman, A. E., Khuon, S., Collins, F. S., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602569103 · Cited by 791
Self-citationLamins A and C but Not Lamin B1 Regulate Nuclear Mechanics
Lammerding, J., Fong, L. G., Ji, J. Y., Reue, K., Stewart, C. L., Young, S. G., & Lee, R. T. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m513511200 · Cited by 688
Nuclear lamin stiffness is a barrier to 3D migration, but softness can limit survival
Harada, T., Swift, J., Irianto, J., Shin, J.-W., Spinler, K. R., Athirasala, A., Diegmiller, R., Dingal, P. C. D. P., Ivanovska, I. L., & Discher, D. E. (2014) · Journal of Cell Biology · doi:10.1083/jcb.201308029 · Cited by 611
Isolated nuclei adapt to force and reveal a mechanotransduction pathway in the nucleus
Guilluy, C., Osborne, L. D., Van Landeghem, L., Sharek, L., Superfine, R., Garcia-Mata, R., & Burridge, K. (2014) · Nature Cell Biology · doi:10.1038/ncb2927 · Cited by 607
Viscoelastic Properties of the Cell Nucleus
Guilak, F., Tedrow, J. R., & Burgkart, R. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.2360 · Cited by 587
Visualizing the molecular sociology at the HeLa cell nuclear periphery
Mahamid, J., Pfeffer, S., Schaffer, M., Villa, E., Danev, R., Kuhn Cuellar, L., Förster, F., Hyman, A. A., Plitzko, J. M., & Baumeister, W. (2016) · Science · doi:10.1126/science.aad8857 · Cited by 576
Shimi, T., Pfleghaar, K., Kojima, S.-I., Pack, C.-G., Solovei, I., Goldman, A. E., Adam, S. A., Shumaker, D. K., Kinjo, M., Cremer, T., et al. (2008) · Genes & Development · doi:10.1101/gad.1735208 · Cited by 519
Self-citationGeneralized Lévy walks and the role of chemokines in migration of effector CD8+ T cells
Harris, T. H., Banigan, E. J., Christian, D. A., Konradt, C., Tait Wojno, E. D., Norose, K., Wilson, E. H., John, B., Weninger, W., Luster, A. D., et al. (2012) · Nature · doi:10.1038/nature11098 · Cited by 512
Self-citationNuclear mechanics during cell migration
Friedl, P., Wolf, K., & Lammerding, J. (2011) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2010.10.015 · Cited by 510
Linear Arrays of Nuclear Envelope Proteins Harness Retrograde Actin Flow for Nuclear Movement
Luxton, G. W. G., Gomes, E. R., Folker, E. S., Vintinner, E., & Gundersen, G. G. (2010) · Science · doi:10.1126/science.1189072 · Cited by 456
Lamin A/C and emerin regulate MKL1–SRF activity by modulating actin dynamics
Ho, C. Y., Jaalouk, D. E., Vartiainen, M. K., & Lammerding, J. (2013) · Nature · doi:10.1038/nature12105 · Cited by 455
The nuclear matrix: Three-dimensional architecture and protein composition
Capco, D. G., Wan, K. M., & Penman, S. (1982) · Cell · doi:10.1016/0092-8674(82)90446-9 · Cited by 433
Dahl, K. N., Kahn, S. M., Wilson, K. L., & Discher, D. E. (2004) · Journal of Cell Science · doi:10.1242/jcs.01357 · Cited by 424
Dahl, K. N., Scaffidi, P., Islam, M. F., Yodh, A. G., Wilson, K. L., & Misteli, T. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601058103 · Cited by 387
Nuclear Mechanics and Mechanotransduction in Health and Disease
Isermann, P., & Lammerding, J. (2013) · Current Biology · doi:10.1016/j.cub.2013.11.009 · Cited by 384
The second decade of 3C technologies: detailed insights into nuclear organization
Denker, A., & de Laat, W. (2016) · Genes & Development · doi:10.1101/gad.281964.116 · Cited by 356
Power-Law Rheology of Isolated Nuclei with Deformation Mapping of Nuclear Substructures
Dahl, K. N., Engler, A. J., Pajerowski, J. D., & Discher, D. E. (2005) · Biophysical Journal · doi:10.1529/biophysj.105.062554 · Cited by 340
Rowat, A. C., Jaalouk, D. E., Zwerger, M., Ung, W. L., Eydelnant, I. A., Olins, D. E., Olins, A. L., Herrmann, H., Weitz, D. A., & Lammerding, J. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.441535 · Cited by 320
Micron-scale coherence in interphase chromatin dynamics
Zidovska, A., Weitz, D. A., & Mitchison, T. J. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1220313110 · Cited by 302
Mechanical Properties of the Cell Nucleus and the Effect of Emerin Deficiency
Rowat, A. C., Lammerding, J., & Ipsen, J. H. (2006) · Biophysical Journal · doi:10.1529/biophysj.106.086454 · Cited by 254
Structural organization of nuclear lamins A, C, B1, and B2 revealed by superresolution microscopy
Shimi, T., Kittisopikul, M., Tran, J., Goldman, A. E., Adam, S. A., Zheng, Y., Jaqaman, K., & Goldman, R. D. (2015) · Molecular Biology of the Cell · doi:10.1091/mbc.e15-07-0461 · Cited by 252
Self-citationThe tethering of chromatin to the nuclear envelope supports nuclear mechanics
Schreiner, S. M., Koo, P. K., Zhao, Y., Mochrie, S. G. J., & King, M. C. (2015) · Nature Communications · doi:10.1038/ncomms8159 · Cited by 244
Nuclear lamin functions and disease
Butin-Israeli, V., Adam, S. A., Goldman, A. E., & Goldman, R. D. (2012) · Trends in Genetics · doi:10.1016/j.tig.2012.06.001 · Cited by 231
Self-citationVerstraeten, V. L. R. M., Ji, J. Y., Cummings, K. S., Lee, R. T., & Lammerding, J. (2008) · Aging Cell · doi:10.1111/j.1474-9726.2008.00382.x · Cited by 212
Valproic Acid Alters Chromatin Structure by Regulation of Chromatin Modulation Proteins
Marchion, D. C., Bicaku, E., Daud, A. I., Sullivan, D. M., & Munster, P. N. (2005) · Cancer Research · doi:10.1158/0008-5472.can-04-2478 · Cited by 212
Taimen, P., Pfleghaar, K., Shimi, T., Möller, D., Ben-Harush, K., Erdos, M. R., Adam, S. A., Herrmann, H., Medalia, O., Collins, F. S., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911895106 · Cited by 211
Self-citationLamins regulate cell trafficking and lineage maturation of adult human hematopoietic cells
Shin, J.-W., Spinler, K. R., Swift, J., Chasis, J. A., Mohandas, N., & Discher, D. E. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1304996110 · Cited by 196
Nuclear lamin stiffness is a barrier to 3D-migration, but softness can limit survival
Harada, T., Swift, J., Irianto, J., Shin, J.-W., Spinler, K. R., Athirasala, A., Diegmiller, R., Dingal, P. C. D. P., Ivanovska, I. L., & Discher, D. E. (2014) · 2014 40th Annual Northeast Bioengineering Conference (NEBEC) · doi:10.1109/nebec.2014.6972810 · Cited by 189
Le Berre, M., Aubertin, J., & Piel, M. (2012) · Integrative Biology · doi:10.1039/c2ib20056b · Cited by 174
Mitotic chromosomes are chromatin networks without a mechanically contiguous protein scaffold
Poirier, M. G., & Marko, J. F. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.232442599 · Cited by 174
Self-citationZwerger, M., Jaalouk, D. E., Lombardi, M. L., Isermann, P., Mauermann, M., Dialynas, G., Herrmann, H., Wallrath, L. L., & Lammerding, J. (2013) · Human Molecular Genetics · doi:10.1093/hmg/ddt079 · Cited by 168
Köster, S., Weitz, D. A., Goldman, R. D., Aebi, U., & Herrmann, H. O. (2015) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2015.01.001 · Cited by 155
Self-citationMechanics and deformation of the nucleus in micropipette aspiration experiment
Vaziri, A., & Mofrad, M. R. K. (2006) · Journal of Biomechanics · doi:10.1016/j.jbiomech.2006.09.023 · Cited by 148
Chromatin decompaction by the nucleosomal binding protein HMGN5 impairs nuclear sturdiness
Furusawa, T., Rochman, M., Taher, L., Dimitriadis, E. K., Nagashima, K., Anderson, S. A., & Bustin, M. (2015) · Nature Communications · doi:10.1038/ncomms7138 · Cited by 141
Mazumder, A., Roopa, T., Basu, A., Mahadevan, L., & Shivashankar, G. V. (2008) · Biophysical Journal · doi:10.1529/biophysj.108.132274 · Cited by 138
Stypula‐Cyrus, Y., Damania, D. P., Kunte, D. P., Cruz, M. D., Subramanian, H., Roy, H. K., & Backman, V. (2013) · PLoS ONE · doi:10.1371/journal.pone.0064600 · Cited by 134
Polach, K. J., Lowary, P. T., & Widom, J. (2000) · Journal of Molecular Biology · doi:10.1006/jmbi.2000.3644 · Cited by 126
Lamin A/C deficiency reduces circulating tumor cell resistance to fluid shear stress
Mitchell, M. J., Denais, C., Chan, M. F., Wang, Z., Lammerding, J., & King, M. R. (2015) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00050.2015 · Cited by 126
Moving Cell Boundaries Drive Nuclear Shaping during Cell Spreading
Li, Y., Lovett, D. B., Zhang, Q., Neelam, S., Kuchibhotla, R. A., Zhu, R., Gundersen, G. G., Lele, T. P., & Dickinson, R. B. (2015) · Biophysical Journal · doi:10.1016/j.bpj.2015.07.006 · Cited by 124
Nongenetic functions of the genome
Bustin, M., & Misteli, T. (2016) · Science · doi:10.1126/science.aad6933 · Cited by 120
Schäpe, J., Prauße, S., Radmacher, M., et al. (2009) · Biophysical Journal · doi:10.1016/j.bpj.2009.02.048 · Cited by 107
Mechanical model of blebbing in nuclear lamin meshworks
Funkhouser, C. M., Sknepnek, R., Shimi, T., Goldman, A. E., Goldman, R. D., & de la Cruz, M. O. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1300215110 · Cited by 104
Self-citationReversible and Irreversible Unfolding of Mitotic Newt Chromosomes by Applied Force
Poirier, M. G., Eroğlu, S., Chatenay, D., & Marko, J. F. (2000) · Molecular Biology of the Cell · doi:10.1091/mbc.11.1.269 · Cited by 103
Self-citationAssessment of Strain Field in Endothelial Cells Subjected to Uniaxial Deformation of Their Substrate
Caille, N., Tardy, Y., & Meister, J.-J. (1998) · Annals of Biomedical Engineering · doi:10.1114/1.132 · Cited by 102
Direct Observation of Nanomechanical Properties of Chromatin in Living Cells
de Vries, A. H. B., Krenn, B. E., DRIEL, R. V., Subramaniam, V., & Kanger, J. S. (2007) · Nano Letters · doi:10.1021/nl070603+ · Cited by 94
Characterization of the elastic properties of the nuclear envelope
Rowat, A. C., Foster, L. J., Nielsen, M. M., Weiss, M., & Ipsen, J. H. (2005) · Journal of The Royal Society Interface · doi:10.1098/rsif.2004.0022 · Cited by 94
Role of Lamin B1 in Chromatin Instability
Butin‐Israeli, V., Adam, S. A., Jain, N., Otte, G. L., Neems, D. S., Wiesmüller, L., Berger, S. L., & Goldman, R. D. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.01145-14 · Cited by 88
Self-citationNuclear Envelope Breakdown Requires Overcoming the Mechanical Integrity of the Nuclear Lamina
Panorchan, P., Schafer, B. W., Wirtz, D., & Tseng, Y. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m402474200 · Cited by 74
Booth, E. A., Spagnol, S. T., Alcoser, T. A., & Dahl, K. N. (2015) · Soft Matter · doi:10.1039/c5sm00521c · Cited by 69
Improved silencing vector co-expressing GFP and small hairpin RNA
Kojima, S.-I., Vignjevic, D. M., & Borisy, G. G. (2004) · BioTechniques · doi:10.2144/04361st02 · Cited by 67
Mitotic chromosomes are constrained by topoisomerase II–sensitive DNA entanglements
Kawamura, R., Pope, L. H., Christensen, M. O., Sun, M., Terekhova, K., Boege, F., Mielke, C., Andersen, A. H., & Marko, J. F. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.200910085 · Cited by 62
Self-citationSimian virus 40 induces lamin A/C fluctuations and nuclear envelope deformation during cell entry
Butin‐Israeli, V., Ben-nun-Shaul, O., Kopatz, I., Adam, S. A., Shimi, T., Goldman, R. D., & Oppenheim, A. (2011) · Nucleus · doi:10.4161/nucl.2.4.16371 · Cited by 47
Self-citationThe nuclear lamina and heterochromatin: a complex relationship
Bank, E. M., & Gruenbaum, Y. (2011) · Biochemical Society Transactions · doi:10.1042/bst20110603 · Cited by 46
Differential Predictive Roles of A- and B-Type Nuclear Lamins in Prostate Cancer Progression
Saarinen, I., Mirtti, T. K., Seikkula, H. A., Boström, P. J., & Taimen, P. (2015) · PLoS ONE · doi:10.1371/journal.pone.0140671 · Cited by 41
The Cellular Mastermind(?)—Mechanotransduction and the Nucleus
Kaminski, A., Fedorchak, G. R., & Lammerding, J. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-394624-9.00007-5 · Cited by 38
Kunte, D. P., Wali, R. K., Koetsier, J. L., Hart, J. A. L., Kostjukova, M. N., Kilimnik, A. Y., Pyatkin, I. G., Strelnikova, S. R., & Roy, H. K. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.05.030 · Cited by 30
Modeling Nuclear Blebs in a Nucleoskeleton of Independent Filament Networks
Wren, N. S., Zhong, Z., Schwartz, R. S., & Dahl, K. N. (2011) · Cellular and Molecular Bioengineering · doi:10.1007/s12195-011-0196-5 · Cited by 17
Cited by
Liquid Nuclear Condensates Mechanically Sense and Restructure the Genome
Shin, Y., Chang, Y.-C., Lee, D. S. W., Berry, J., Sanders, D. W., Ronceray, P., Wingreen, N. S., Haataja, M., & Brangwynne, C. P. (2018) · Cell · doi:10.1016/j.cell.2018.10.057 · Cited by 676
Mechanics and functional consequences of nuclear deformations
Kalukula, Y., Stephens, A. D., Lammerding, J., & Gabriele, S. (2022) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-022-00480-z · Cited by 475
Self-citationRegulation of genome organization and gene expression by nuclear mechanotransduction
Uhler, C., & Shivashankar, G. V. (2017) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2017.101 · Cited by 445
Chromatin histone modifications and rigidity affect nuclear morphology independent of lamins
Stephens, A. D., Liu, P. Z., Banigan, E. J., Almassalha, L. M., Backman, V., Adam, S. A., Goldman, R. D., & Marko, J. F. (2018) · Molecular Biology of the Cell · doi:10.1091/mbc.e17-06-0410 · Cited by 353
Self-citationCondensed Chromatin Behaves like a Solid on the Mesoscale In Vitro and in Living Cells
Strickfaden, H., Tolsma, T. O., Sharma, A., Underhill, D. A., Hansen, J. C., & Hendzel, M. J. (2020) · Cell · doi:10.1016/j.cell.2020.11.027 · Cited by 283
Metadata
- Authors
- Stephens, A. D., Banigan, E. J., Adam, S. A., Goldman, R. D., & Marko, J. F.
- Venue
- Molecular Biology of the Cell
- Published
- 2017-07-07
- Volume
- 28
- Issue
- 14
- Pages
- 1984-1996
- ISSN
- 1059-1524 (ISSN-L)
- 1939-4586
- OpenAlex
- W2571383784
- Cited by
- 473
- References
- 71
- FWCI
- 13.78
- Type
- journal article
- Language
- en
- Open access
- green
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.