The septin cytoskeleton facilitates membrane retraction during motility and blebbing
Open accessAbstract
Increasing evidence supports a critical role for the septin cytoskeleton at the plasma membrane during physiological processes including motility, formation of dendritic spines or cilia, and phagocytosis. We sought to determine how septins regulate the plasma membrane, focusing on this cytoskeletal element's role during effective amoeboid motility. Surprisingly, septins play a reactive rather than proactive role, as demonstrated during the response to increasing hydrostatic pressure and subsequent regulatory volume decrease. In these settings, septins were required for rapid cortical contraction, and SEPT6-GFP was recruited into filaments and circular patches during global cortical contraction and also specifically during actin filament depletion. Recruitment of septins was also evident during excessive blebbing initiated by blocking membrane trafficking with a dynamin inhibitor, providing further evidence that septins are recruited to facilitate retraction of membranes during dynamic shape change. This function of septins in assembling on an unstable cortex and retracting aberrantly protruding membranes explains the excessive blebbing and protrusion observed in septin-deficient T cells.
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
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.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Functional perturbation of proteins that direct the formation and/or regulation of the cytokinetic furrow results in similar plasma membrane blebbing during mitosis.
“Previous studies have demonstrated that functional perturbation of proteins that direct the formation and/or regulation of the cytokinetic furrow results in similar plasma membrane blebbing during mitosis [17, 28].”
From Tumor Treating Fields Perturb the Localization of Septins and Cause Aberrant Mitotic Exit (2015) · cites this paper as [28]
Knockdown of Septin 2, 6 or 7 results in similar violent membrane blebbing and abnormal mitotic exit.
“Indeed, knockdown of Septin 2, 6 or 7 has been shown to result in similar violent membrane blebbing and abnormal mitotic exit [28, 29]”
From Tumor Treating Fields Perturb the Localization of Septins and Cause Aberrant Mitotic Exit (2015) · cites this paper as [28]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Lifeact: a versatile marker to visualize F-actin
Riedl, J., Crevenna, A. H., Kessenbrock, K., Yu, J. H., Neukirchen, D., Bista, M., Bradke, F., Jenne, D., Holak, T. A., Werb, Z., et al. (2008) · Nature Methods · doi:10.1038/nmeth.1220 · Cited by 2,189 · see citing works
Sahai, E. A., & Marshall, C. J. (2003) · Nature Cell Biology · doi:10.1038/ncb1019 · Cited by 1,148 · see citing works
Hydrostatic pressure and the actomyosin cortex drive mitotic cell rounding
Stewart, M. P., Helenius, J. H., Toyoda, Y., Ramanathan, S. P., Müller, D. J., & Hyman, A. A. (2010) · Nature · doi:10.1038/nature09642 · Cited by 679 · see citing works
Reassembly of contractile actin cortex in cell blebs
Charras, G., Hu, C., Coughlin, M. L., & Mitchison, T. J. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200602085 · Cited by 620 · see citing works
Cell motility through plasma membrane blebbing
Fackler, O., & Grosse, R. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200802081 · Cited by 588 · see citing works
Self- and actin-templated assembly of Mammalian septins
Kinoshita, M., Field, C. M., Coughlin, M. L., Straight, A. F., & Mitchison, T. J. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00366-0 · Cited by 526 · see citing works
Hu, Q., Milenković, L., Jin, H., Scott, M. P., Nachury, M. V., Spiliotis, E. T., & Nelson, W. J. (2010) · Science · doi:10.1126/science.1191054 · Cited by 513 · see citing works
Cell control by membrane–cytoskeleton adhesion
Sheetz, M. P. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35073095 · Cited by 478 · see citing works
Life and Times of a Cellular Bleb
Charras, G., Coughlin, M. L., Mitchison, T. J., & Mahadevan, L. (2007) · Biophysical Journal · doi:10.1529/biophysj.107.113605 · Cited by 456 · see citing works
Responses of lymphocytes to anisotonic media: volume-regulating behavior
Grinstein, S., Rothstein, A., Sarkadi, B., & Gelfand, E. W. (1984) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1984.246.3.c204 · Cited by 427 · see citing works
Migration of Zebrafish Primordial Germ Cells: A Role for Myosin Contraction and Cytoplasmic Flow
Blaser, H., Reichman‐Fried, M., Castanon, I., Dumstrei, K., Marlow, F. L., Kawakami, K., Solnica‐Krezel, L., Heisenberg, C., & Raz, E. (2006) · Developmental Cell · doi:10.1016/j.devcel.2006.09.023 · Cited by 406 · see citing works
Kinoshita, M., Kumar, S., Mizoguchi, A., Idé, C., Kinoshita, A., Haraguchi, T., Hiraoka, Y., & Noda, M. (1997) · Genes & Development · doi:10.1101/gad.11.12.1535 · Cited by 380 · see citing works
Hsu, S.-C., Hazuka, C. D., Roth, R. A., Foletti, D. L., Heuser, J., & Scheller, R. H. (1998) · Neuron · doi:10.1016/s0896-6273(00)80493-6 · Cited by 358 · see citing works
The septin cortex at the yeast mother–bud neck
Gladfelter, A. S. (2001) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(01)00269-7 · Cited by 331 · see citing works
Ihara, M., Kinoshita, A., Yamada, S., Tanaka, H., Tanigaki, A., Kitano, A., Goto, M., Okubo, K., Nishiyama, H., Ogawa, O., et al. (2005) · Developmental Cell · doi:10.1016/j.devcel.2004.12.005 · Cited by 294 · see citing works
Role of Septin Cytoskeleton in Spine Morphogenesis and Dendrite Development in Neurons
Tada, T., Simonetta, A., Batterton, M. N., Kinoshita, M., Edbauer, D., & Sheng, M. (2007) · Current Biology · doi:10.1016/j.cub.2007.09.039 · Cited by 284 · see citing works
Kinoshita, M. (2003) · The Journal of Biochemistry · doi:10.1093/jb/mvg182 · Cited by 283 · see citing works
Bertin, A., McMurray, M. A., Thai, L., García, G., Votin, V., Grob, P., Allyn, T., Thorner, J. W., & Nogales, E. (2010) · Journal of Molecular Biology · doi:10.1016/j.jmb.2010.10.002 · Cited by 272 · see citing works
The Mammalian Septin MSF Localizes with Microtubules and Is Required for Completion of Cytokinesis
Surka, M. C., Tsang, C. W., & Trimble, W. S. (2002) · Molecular Biology of the Cell · doi:10.1091/mbc.e02-01-0042 · Cited by 266 · see citing works
Pseudopodial Actin Dynamics Control Epithelial-Mesenchymal Transition in Metastatic Cancer Cells
Shankar, J., Messenberg, A., Chan, J. K. Y., et al. (2010) · Cancer Research · doi:10.1158/0008-5472.can-09-4439 · Cited by 263 · see citing works
A Mitotic Septin Scaffold Required for Mammalian Chromosome Congression and Segregation
Spiliotis, E. T., Kinoshita, M., & Nelson, W. J. (2005) · Science · doi:10.1126/science.1106823 · Cited by 256 · see citing works
The GTP-Binding Protein Septin 7 Is Critical for Dendrite Branching and Dendritic-Spine Morphology
Xie, Y., Vessey, J. P., Konecna, A., Dahm, R., Macchi, P., & Kiebler, M. A. (2007) · Current Biology · doi:10.1016/j.cub.2007.08.042 · Cited by 255 · see citing works
Mammalian SEPT2 Is Required for Scaffolding Nonmuscle Myosin II and Its Kinases
Joo, E. E., Surka, M. C., & Trimble, W. S. (2007) · Developmental Cell · doi:10.1016/j.devcel.2007.09.001 · Cited by 227 · see citing works
Septin-Mediated Uniform Bracing of Phospholipid Membranes
Tanaka-Takiguchi, Y., Kinoshita, M., & Takiguchi, K. (2009) · Current Biology · doi:10.1016/j.cub.2008.12.030 · Cited by 203 · see citing works
Tooley, A. J., Gilden, J., Jacobelli, J., Beemiller, P., Trimble, W. S., Kinoshita, M., & Krummel, M. F. (2009) · Nature Cell Biology · doi:10.1038/ncb1808 · Cited by 189 · cited 7× · see citing works
“This appears at odds with the observation that the majority of septin aggregates are present along the T cell uropod (Tooley et al., 2009).”
InfluentialSelf-citationPtdIns(4,5)P2 Functions at the Cleavage Furrow during Cytokinesis
Field, S. J., Madson, N., Kerr, M. L., Galbraith, K. A. A., Kennedy, C. E., Tahiliani, M., Wilkins, A., & Cantley, L. C. (2005) · Current Biology · doi:10.1016/j.cub.2005.06.059 · Cited by 188 · see citing works
Nagata, K., Kawajiri, A., Matsui, S., Takagishi, M., Shiromizu, T., Saitoh, N., Izawa, I., Kiyono, T., Itoh, T. J., Hotani, H., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m205246200 · Cited by 186 · see citing works
Actin and Septin Ultrastructures at the Budding Yeast Cell Cortex
Rodal, A. A., Kozubowski, L., Goode, B. L., Drubin, D. G., & Hartwig, J. H. (2004) · Molecular Biology of the Cell · doi:10.1091/mbc.e04-08-0734 · Cited by 182 · see citing works
Osaka, M., Rowley, J. D., & Zeleznik‐Le, N. J. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.11.6428 · Cited by 172 · see citing works
Ihara, M., Yamasaki, N., Hagiwara, A., Tanigaki, A., Kitano, A., Hikawa, R., Tomimoto, H., Noda, M., Takanashi, M., Mori, H., et al. (2007) · Neuron · doi:10.1016/j.neuron.2007.01.019 · Cited by 165 · see citing works
Implications of a poroelastic cytoplasm for the dynamics of animal cell shape
Mitchison, T. J., Charras, G., & Mahadevan, L. (2008) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2008.01.008 · Cited by 159 · see citing works
Proteolytic and non-proteolytic migration of tumour cells and leucocytes
Friedl, P., & Wolf, K. (2003) · Biochemical Society Symposia · doi:10.1042/bss0700277 · Cited by 148 · see citing works
Mechanisms of force generation and force transmission during interstitial leukocyte migration
Renkawitz, J., & Sixt, M. (2010) · EMBO Reports · doi:10.1038/embor.2010.147 · Cited by 145 · see citing works
Montagna, C., Lyu, M. S., Hunter, K. W., Lukes, L., Lowther, W. J., Reppert, T., Hissong, B. D., Weaver, Z., & Ried, T. (2003) · PubMed · Cited by 142 · see citing works
Nguyen, T. Q., Sawa, H., Okano, H., et al. (2000) · Journal of Cell Science · doi:10.1242/jcs.113.21.3825 · Cited by 137 · see citing works
Role of the Na+/H+ exchanger NHE1 in cell migration
Stock, C. M., & Schwab, A. (2006) · Acta Physiologica · doi:10.1111/j.1748-1716.2006.01543.x · Cited by 132 · see citing works
A prototypic platelet septin and its participation in secretion
Dent, J. A., Kato, K., Peng, X., Martı́nez, C., Cattaneo, M., Poujol, C., Nurden, P., Nurden, A. T., Trimble, W. S., & Ware, J. L. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.052715199 · Cited by 129 · see citing works
Control of cortical rigidity by the cytoskeleton: Emerging roles for septins
Gilden, J. K., & Krummel, M. F. (2010) · Cytoskeleton · doi:10.1002/cm.20461 · Cited by 119 · see citing works
Self-citationMammalian Septins Are Required for Phagosome Formation
Huang, Y., Yan, M., Collins, R. F., DiCiccio, J. E., Grinstein, S., & Trimble, W. S. (2008) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-07-0641 · Cited by 114 · see citing works
Connolly, D., Yang, Z., Castaldi, M. T., Simmons, N., Oktay, M. H., Coniglio, S. J., Fazzari, M. J., Verdier‐Pinard, P., & Montagna, C. (2011) · Breast Cancer Research · doi:10.1186/bcr2924 · Cited by 111 · see citing works
Role of the F-actin Cytoskeleton in the RVD and RVI Processes in Ehrlich Ascites Tumor Cells
Pedersen, S. F., Mills, J. W., & Hoffmann, E. K. (1999) · Experimental Cell Research · doi:10.1006/excr.1999.4615 · Cited by 103 · see citing works
Blebbing of Dictyostelium cells in response to chemoattractant
Langridge, P. D., & Kay, R. R. (2006) · Experimental Cell Research · doi:10.1016/j.yexcr.2006.03.007 · Cited by 90 · see citing works
Cornet, M., Lambert, I. H., & Hoffmann, E. K. (1993) · The Journal of Membrane Biology · doi:10.1007/bf02258534 · Cited by 83 · see citing works
Changes of actin cytoskeleton during swelling and regulatory volume decrease in cultured astrocytes
Morán, J., Sabanero, M., Meza, I., & Pasantes‐Morales, H. (1996) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1996.271.6.c1901 · Cited by 60 · see citing works
SEPT9_v4 expression induces morphological change, increased motility and disturbed polarity
Chacko, A. D., Hyland, P. L., McDade, S. S., Hamilton, P. W., Russell, S. H., & Hall, P. A. (2005) · The Journal of Pathology · doi:10.1002/path.1794 · Cited by 51 · see citing works
Carton, I., Hermans, D., & Eggermont, J. (2003) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00069.2003 · Cited by 37 · see citing works
GPI anchoring facilitates propagation and spread of misfolded Sup35 aggregates in mammalian cells
Speare, J. O., Offerdahl, D. K., Hasenkrug, A. M., Carmody, A., & Baron, G. S. (2010) · The EMBO Journal · doi:10.1038/emboj.2009.392 · Cited by 26 · see citing works
Tamma, G., Procino, G., Svelto, M., & Valenti, G. (2007) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00375.2006 · Cited by 26 · see citing works
Nielsen, D. K., Jensen, A. K., Harbak, H., Christensen, S. C., & Simonsen, L. O. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.132308 · Cited by 22 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Tumor Treating Fields Perturb the Localization of Septins and Cause Aberrant Mitotic Exit
Gera, N., Yang, A., Holtzman, T. S., Lee, S. X., Wong, E. T., & Swanson, K. D. (2015) · PLOS ONE · doi:10.1371/journal.pone.0125269 · Cited by 217 · see citing works
An Evidence-Based Review of Alternating Electric Fields Therapy for Malignant Gliomas
Wong, E. T., Lok, E., & Swanson, K. D. (2015) · Current Treatment Options in Oncology · doi:10.1007/s11864-015-0353-5 · Cited by 35 · see citing works
- Authors
- Gilden, J. K., Peck, S., M. Chen, Y.-C., & Krummel, M. F.
- Affiliations
- University of California, San Francisco (US)
- Department of Pathology 1 and 2
- Corresponding author
- Krummel, Matthew F.
- Venue
- Journal of Cell Biology
- Publisher
- Rockefeller University Press
- Published
- 2012-01-09
- Volume
- 196
- Issue
- 1
- Pages
- 103-114
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- PMC
- PMC3255977
- OpenAlex
- W2099127112
- Cited by
- 113
- References
- 49
- Citations by year
- 2026: 8 · 2025: 1 · 2024: 5 · 2023: 11 · 2022: 14 · 2021: 9 · 2020: 7 · 2019: 5 · 2018: 10 · 2017: 5 · 2016: 11 · 2015: 11 · 2014: 12 · 2013: 3 · 2012: 1
- FWCI
- 4.09
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by-nc-sa
- Locations
- The Journal of Cell Biology (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- eScholarship (California Digital Library) (submittedVersion, cc-by-nc-sa)
- Funders
- National Science Foundation
- National Institutes of Health
- National Institute of Allergy and Infectious Diseases (R01AI52116, R01AI052116)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Keywords
- septins, amoeboid movement, blebbing, cortical contraction, regulatory volume decrease, hydrostatic pressure, membrane trafficking, plasma membrane
- MeSH terms
- Actomyosin, Animals, Biological Transport, Cell Line, Cell Membrane, Cell Movement, Cytoskeleton, Recombinant Fusion Proteins, Green Fluorescent Proteins, Mice, Septins
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