The postmitotic midbody: Regulating polarity, stemness, and proliferation
Open accessAbstract
Abscission, the final stage of cell division, requires well-orchestrated changes in endocytic trafficking, microtubule severing, actin clearance, and the physical sealing of the daughter cell membranes. These processes are highly regulated, and any missteps in localized membrane and cytoskeleton dynamics often lead to a delay or a failure in cell division. The midbody, a microtubule-rich structure that forms during cytokinesis, is a key regulator of abscission and appears to function as a signaling platform coordinating cytoskeleton and endosomal dynamics during the terminal stages of cell division. It was long thought that immediately following abscission and the conclusion of cell division, the midbody is either released or rapidly degraded by one of the daughter cells. Recently, the midbody has gained prominence for exerting postmitotic functions. In this review, we detail the role of the midbody in orchestrating abscission, as well as discuss the relatively new field of postabscission midbody biology, particularly focusing on how it may act to regulate cell polarity and its potential to regulate cell tumorigenicity or stemness.
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Release of the spindle midbody during abscission was visualized.
“Importantly, we could also directly visualize how one of the half-spindle remnants often repositions to the cytoplasmic bridge formed by the midzone MTs after anaphase (Piel et al., 2001) and the release of the spindle midbody during abscission (Peterman and Prekeris 2019).”
From A live-cell marker to visualize the dynamics of stable microtubules throughout the cell cycle (2023) · cites this paper as Peterman and Prekeris 2019
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Every step of the way: integrins in cancer progression and metastasis
Hamidi, H., & Ivaska, J. (2018) · Nature Reviews Cancer · doi:10.1038/s41568-018-0038-z · Cited by 1,493 · see citing works
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Research works printed but not linked: 77
- Allison R., Lumb J.H., Fassier C., Connell J.W., Ten Martin D., Seaman M.N.J., Hazan J., and Reid E. 2013 An ESCRT-spastin interaction promotes fission of recycling tubules from the endosome. J. Cell Biol. 202: 527– 543. 10.1083/jcb.201211045 23897888 PMC3734076 · DOI
- Amon A. 1999 The spindle checkpoint. Curr. Opin. Genet. Dev. 9: 69– 75. 10.1016/S0959-437X(99)80010-0 10072359 · DOI
- Armenti S.T., Chan E., and Nance J. 2014 Polarized exocyst-mediated vesicle fusion directs intracellular lumenogenesis within the C. elegans excretory cell. Dev. Biol. 394: 110– 121. 10.1016/j.ydbio.2014.07.019 25102190 PMC4373406 · DOI
- Atilla-Gokcumen G.E., Muro E., Relat-Goberna J., Sasse S., Bedigian A., Coughlin M.L., Garcia-Manyes S., and Eggert U.S. 2014 Dividing cells regulate their lipid composition and localization. Cell. 156: 428– 439. 10.1016/j.cell.2013.12.015 24462247 PMC3909459 · DOI
- Bai X., Lee P.-Y., Chen C.-Y., Simmons J.R., Nebenfuehr B., Mitchell D., Klebanow L.R., Mattson N., Sorensen C.G. Turpin B.-C. Chen, 2018 Aurora B Is Required for Programmed Variations of Cytokinesis during Morphogenesis in the C. Elegans Embryo. bioRxiv. doi:10.1101/319657 (Preprint posted August 27, 2018). · DOI
- Bajorek M., Schubert H.L., McCullough J., Langelier C., Eckert D.M., Stubblefield W.M., Uter N.T., Myszka D.G., Hill C.P., and Sundquist W.I. 2009 Structural basis for ESCRT-III protein autoinhibition. Nat. Struct. Mol. Biol. 16: 754– 762. 10.1038/nsmb.1621 19525971 PMC2712734 · DOI
- Barker N., van Es J.H., Kuipers J., Kujala P., van den Born M., Cozijnsen M., Haegebarth A., Korving J., Begthel H., Peters P.J., and Clevers H. 2007 Identification of stem cells in small intestine and colon by marker gene Lgr5. Nature. 449: 1003– 1007. 10.1038/nature06196 17934449 · DOI · Paper page
- Barrow-McGee R., Kishi N., Joffre C., Ménard L., Hervieu A., Bakhouche B.A., Noval A.J., Mai A., Guzmán C., Robbez-Masson L., 2016 Beta 1-integrin-c-Met cooperation reveals an inside-in survival signalling on autophagy-related endomembranes. Nat. Commun. 7: 11942 10.1038/ncomms11942 27336951 PMC4931016 · DOI
- Bernabé-Rubio M., Andrés G., Casares-Arias J., Fernández-Barrera J., Rangel L., Reglero-Real N., Gershlick D.C., Fernández J.J., Millán J., Correas I., 2016 Novel Role for the Midbody in Primary Ciliogenesis by Polarized Epithelial Cells. J. Cell Biol. 214: 259– 273. 10.1083/jcb.201601020 27458130 PMC4970324 · DOI
- Capalbo L., Bassi Z.I., Geymonat M., Todesca S., Copoiu L., Enright A.J., Callaini G., Riparbelli M.G., Yu L., Choudhary J.S., 2019 The midbody interactome reveals unexpected roles for PP1 phosphatases in cytokinesis. Nat. Commun. 10: 4513 10.1038/s41467-019-12507-9 31586073 PMC6778137 · DOI
- Capalbo L., Montembault E., Takeda T., Bassi Z.I., Glover D.M., and D’Avino P.P. 2012 The chromosomal passenger complex controls the function of endosomal sorting complex required for transport-III Snf7 proteins during cytokinesis. Open Biol. 2: 120070 10.1098/rsob.120070 22724069 PMC3376741 · DOI
- Cashikar A.G., Shim S., Roth R., Maldazys M.R., Heuser J.E., and Hanson P.I. 2014 Structure of Cellular ESCRT-III Spirals and Their Relationship to HIV Budding. eLife. 3: e02184 10.7554/eLife.02184 PMC4073282 24878737 · DOI · Paper page
- Chai Y., Tian D., Yang Y., Feng G., Cheng Z., Li W., and Ou G. 2012 Apoptotic regulators promote cytokinetic midbody degradation in C. elegans. J. Cell Biol. 199: 1047– 1055. 10.1083/jcb.201209050 23253479 PMC3529525 · DOI
- Christ L., Raiborg C., Wenzel E.M., Campsteijn C., and Stenmark H. 2017 Cellular Functions and Molecular Mechanisms of the ESCRT Membrane-Scission Machinery. Trends Biochem. Sci. 42: 42– 56. 10.1016/j.tibs.2016.08.016 27669649 · DOI
- Christ L., Wenzel E.M., Liestøl K., Raiborg C., Campsteijn C., and Stenmark H. 2016 ALIX and ESCRT-I/II function as parallel ESCRT-III recruiters in cytokinetic abscission. J. Cell Biol. 212: 499– 513. 10.1083/jcb.201507009 26929449 PMC4772496 · DOI · Paper page
- Crowell E.F., Gaffuri A.L., Gayraud-Morel B., Tajbakhsh S., and Echard A. 2014 Engulfment of the midbody remnant after cytokinesis in mammalian cells. J. Cell Sci. 127: 3840– 3851. 10.1242/jcs.154732 25002399 · DOI
- D’Avino P.P. 2017 Citron kinase - renaissance of a neglected mitotic kinase. J. Cell Sci. 130: 1701– 1708. 10.1242/jcs.200253 28468989 · DOI
- D’Avino P.P., Savoian M.S., and Glover D.M. 2005 Cleavage furrow formation and ingression during animal cytokinesis: a microtubule legacy. J. Cell Sci. 118: 1549– 1558. 10.1242/jcs.02335 15811947 · DOI
- Dambournet D., Machicoane M., Chesneau L., Sachse M., Rocancourt M., El Marjou A., Formstecher E., Salomon R., Goud B., and Echard A. 2011 Rab35 GTPase and OCRL phosphatase remodel lipids and F-actin for successful cytokinesis. Nat. Cell Biol. 13: 981– 988. 10.1038/ncb2279 21706022 · DOI
- Daniel E., Daud M., Kolotuev I., Charish K., Auld V., and Le Borgne R. 2018 Coordination of Septate Junctions Assembly and Completion of Cytokinesis in Proliferative Epithelial Tissues. Curr. Biol. 28: 1380– 1391.e4. 10.1016/j.cub.2018.03.034 29706514 · DOI
- Dionne L.K., Peterman E., Schiel J., Gibieža P., Skeberdis V.A., Jimeno A., Wang X.-J., and Prekeris R. 2017 FYCO1 Regulates Accumulation of Post-Mitotic Midbodies by Mediating LC3-Dependent Midbody Degradation. J. Cell Sci. 130: 4051– 4062. 10.1242/jcs.208983 29196475 PMC5769594 · DOI
- Distel M., Hocking J.C., and Köster R.W. 2011 In vivo cell biology using Gal4-mediated multicolor subcellular labeling in zebrafish. Commun. Integr. Biol. 4: 336– 339. 10.4161/cib.4.3.15037 21980574 PMC3187902 · DOI
- Dupuy A.G., and Caron E. 2008 Integrin-dependent phagocytosis: spreading from microadhesion to new concepts. J. Cell Sci. 121: 1773– 1783. 10.1242/jcs.018036 18492791 · DOI
- Elia N., Sougrat R., Spurlin T.A., Hurley J.H., and Lippincott-Schwartz J. 2011 Dynamics of Endosomal Sorting Complex Required for Transport (ESCRT) Machinery during Cytokinesis and Its Role in Abscission. Proc. Natl. Acad. Sci. USA. 108: 4846– 4851. 10.1073/pnas.1102714108 21383202 PMC3064317 · DOI
- Ettinger A.W., Wilsch-Bräuninger M., Marzesco A.M., Bickle M., Lohmann A., Maliga Z., Karbanová J., Corbeil D., Hyman A.A., and Huttner W.B. 2011 Proliferating versus differentiating stem and cancer cells exhibit distinct midbody-release behaviour. Nat. Commun. 2: 503 10.1038/ncomms1511 22009035 PMC3207209 · DOI
- Fededa J.P., and Gerlich D.W. 2012 Molecular control of animal cell cytokinesis. Nat. Cell Biol. 14: 440– 447. 10.1038/ncb2482 22552143 · DOI
- Flannagan R.S., Jaumouillé V., and Grinstein S. 2012 The cell biology of phagocytosis. Annu. Rev. Pathol. 7: 61– 98. 10.1146/annurev-pathol-011811-132445 21910624 · DOI
- Forth S., and Kapoor T.M. 2017 The mechanics of microtubule networks in cell division. J. Cell Biol. 216: 1525– 1531. 10.1083/jcb.201612064 28490474 PMC5461028 · DOI
- Girdler G.C., Araya C., Ren X., and Clarke J.D.W. 2013 Developmental Time Rather than Local Environment Regulates the Schedule of Epithelial Polarization in the Zebrafish Neural Rod. Neural Dev. 8: 5 10.1186/1749-8104-8-5 23521850 PMC3623869 · DOI
- Gnazzo M.M., Uhlemann E.E., Villarreal A.R., Shirayama M., Dominguez E.G., and Skop A.R. 2016 The RNA-binding protein ATX-2 regulates cytokinesis through PAR-5 and ZEN-4. Mol. Biol. Cell. 27: 3052– 3064. 10.1091/mbc.e16-04-0219 27559134 PMC5063614 · DOI
- Goliand I., Adar-Levor S., Segal I., Nachmias D., Dadosh T., Kozlov M.M., and Elia N. 2018 Resolving ESCRT-III Spirals at the Intercellular Bridge of Dividing Cells Using 3D STORM. Cell Reports. 24: 1756– 1764. 10.1016/j.celrep.2018.07.051 30110633 · DOI
- Guizetti J., Schermelleh L., Mäntler J., Maar S., Poser I., Leonhardt H., Müller-Reichert T., and Gerlich D.W. 2011 Cortical constriction during abscission involves helices of escrt-iii–dependent filaments. Science. 331: 1616– 1620. 10.1126/science.1201847 21310966 · DOI
- Guo W., Pylayeva Y., Pepe A., Yoshioka T., Muller W.J., Inghirami G., and Giancotti F.G. 2006 Beta 4 integrin amplifies ErbB2 signaling to promote mammary tumorigenesis. Cell. 126: 489– 502. 10.1016/j.cell.2006.05.047 16901783 · DOI
- Haegebarth A., and Clevers H. 2009 Wnt signaling, lgr5, and stem cells in the intestine and skin. Am. J. Pathol. 174: 715– 721. 10.2353/ajpath.2009.080758 19197002 PMC2665733 · DOI
- Henne W.M., Buchkovich N.J., and Emr S.D. 2011 The ESCRT pathway. Dev. Cell. 21: 77– 91. 10.1016/j.devcel.2011.05.015 21763610 · DOI
- Higashi T., Arnold T.R., Stephenson R.E., Dinshaw K.M., and Miller A.L. 2016 Maintenance of the Epithelial Barrier and Remodeling of Cell-Cell Junctions during Cytokinesis. Curr. Biol. 26: 1829– 1842. 10.1016/j.cub.2016.05.036 27345163 PMC5884674 · DOI
- Jones T.A., Nikolova L.S., Schjelderup A., and Metzstein M.M. 2014 Exocyst-mediated membrane trafficking is required for branch outgrowth in Drosophila tracheal terminal cells. Dev. Biol. 390: 41– 50. 10.1016/j.ydbio.2014.02.021 24607370 PMC4041209 · DOI
- Karasmanis E.P., Hwang D., Nakos K., Bowen J.R., Angelis D., and Spiliotis E.T. 2019 A Septin Double Ring Controls the Spatiotemporal Organization of the ESCRT Machinery in Cytokinetic Abscission. Curr. Biol. 29: 2174– 2182.e7. 10.1016/j.cub.2019.05.050 31204162 PMC6620605 · DOI
- Klinkert K., Rocancourt M., Houdusse A., and Echard A. 2016 Rab35 GTPase couples cell division with initiation of epithelial apico-basal polarity and lumen opening. Nat. Commun. 7: 11166 10.1038/ncomms11166 27040773 PMC4822036 · DOI
- König J., Frankel E.B., Audhya A., and Müller-Reichert T. 2017 Membrane remodeling during embryonic abscission in Caenorhabditis elegans. J. Cell Biol. 216: 1277– 1286. 10.1083/jcb.201607030 28325808 PMC5412558 · DOI
- Kouranti I., Sachse M., Arouche N., Goud B., and Echard A. 2006 Rab35 regulates an endocytic recycling pathway essential for the terminal steps of cytokinesis. Curr. Biol. 16: 1719– 1725. 10.1016/j.cub.2006.07.020 16950109 · DOI
- Kuo T.C., Chen C.T., Baron D., Onder T.T., Loewer S., Almeida S., Weismann C.M., Xu P., Houghton J.M., Gao F.B., 2011 Midbody accumulation through evasion of autophagy contributes to cellular reprogramming and tumorigenicity. Nat. Cell Biol. 13: 1214– 1223. 10.1038/ncb2332 21909099 PMC4208311 · DOI
- Lafaurie-Janvore J., Maiuri P., Wang I., Pinot M., Manneville J.B., Betz T., Balland M., and Piel M. 2013 ESCRT-III assembly and cytokinetic abscission are induced by tension release in the intercellular bridge. Science. 339: 1625– 1629. 10.1126/science.1233866 23539606 · DOI
- Lata S., Schoehn G., Jain A., Pires R., Piehler J., Gottlinger H.G., and Weissenhorn W. 2008 Helical structures of ESCRT-III are disassembled by VPS4. Science. 321: 1354– 1357. 10.1126/science.1161070 18687924 PMC2758909 · DOI
- Le Bras S., and Le Borgne R. 2014 Epithelial cell division - multiplying without losing touch. J. Cell Sci. 127: 5127– 5137. 10.1242/jcs.151472 25344250 · DOI
- Li D., Mangan A., Cicchini L., Margolis B., and Prekeris R. 2014 FIP5 phosphorylation during mitosis regulates apical trafficking and lumenogenesis. EMBO Rep. 15: 428– 437. 10.1002/embr.201338128 24591568 PMC3989674 · DOI
- London N., and Biggins S. 2014 Signalling dynamics in the spindle checkpoint response. Nat. Rev. Mol. Cell Biol. 15: 736– 747. 10.1038/nrm3888 25303117 PMC4283840 · DOI
- Lujan P., Rubio T., Varsano G., and Köhn M. 2017 Keep it on the edge: The postmitotic midbody as a polarity signal unit. Commun. Integr. Biol. 10: e1338990 10.1080/19420889.2017.1338990 28919938 PMC5595415 · DOI
- Mangan A.J., Sietsema D.V., Li D., Moore J.K., Citi S., and Prekeris R. 2016 Cingulin and actin mediate midbody-dependent apical lumen formation during polarization of epithelial cells. Nat. Commun. 7: 12426 10.1038/ncomms12426 27484926 PMC4976216 · DOI
- McNally F.J., and Roll-Mecak A. 2018 Microtubule-severing enzymes: From cellular functions to molecular mechanism. J. Cell Biol. 217: 4057– 4069. 10.1083/jcb.201612104 30373906 PMC6279391 · DOI
- Mierzwa B., and Gerlich D.W. 2014 Cytokinetic abscission: molecular mechanisms and temporal control. Dev. Cell. 31: 525– 538. 10.1016/j.devcel.2014.11.006 25490264 · DOI
- Mierzwa B.E., Chiaruttini N., Redondo-Morata L., von Filseck J.M., König J., Larios J., Poser I., Müller-Reichert T., Scheuring S., Roux A., and Gerlich D.W. 2017 Dynamic subunit turnover in ESCRT-III assemblies is regulated by Vps4 to mediate membrane remodelling during cytokinesis. Nat. Cell Biol. 19: 787– 798. 10.1038/ncb3559 28604678 PMC5493987 · DOI
- Miyamoto S., Teramoto H., Gutkind J.S., and Yamada K.M. 1996 Integrins can collaborate with growth factors for phosphorylation of receptor tyrosine kinases and MAP kinase activation: roles of integrin aggregation and occupancy of receptors. J. Cell Biol. 135: 1633– 1642. 10.1083/jcb.135.6.1633 8978828 PMC2133938 · DOI
- Ou G., Gentili C., and Gönczy P. 2014 Stereotyped Distribution of Midbody Remnants in Early C. Elegans Embryos Requires Cell Death Genes and Is Dispensable for Development. Cell Res. 24: 251– 253. 10.1038/cr.2013.140 24126714 PMC3916897 · DOI
- Peterman E., and Prekeris R. 2017 Understanding Post-Mitotic Roles of the Midbody during Cell Differentiation and Polarization. Methods Cell Biol. 137: 173– 186. 10.1016/bs.mcb.2016.04.001 28065304 PMC5488711 · DOI
- Peterman E., Gibieža P., Schafer J., Skeberdis V.A., Kaupinis A., Valius M., Heiligenstein X., Hurbain I., Raposo G., and Prekeris R. 2019 The post-abscission midbody is an intracellular signaling organelle that regulates cell proliferation. Nat. Commun. 10: 3181 10.1038/s41467-019-10871-0 31320617 PMC6639393 · DOI
- Pollard T.D. 2010 Mechanics of cytokinesis in eukaryotes. Curr. Opin. Cell Biol. 22: 50– 56. 10.1016/j.ceb.2009.11.010 20031383 PMC2871152 · DOI
- Pollard T.D. 2017 Nine unanswered questions about cytokinesis. J. Cell Biol. 216: 3007– 3016. 10.1083/jcb.201612068 28807993 PMC5626534 · DOI
- Pollarolo G., Schulz J.G., Munck S., and Dotti C.G. 2011 Cytokinesis remnants define first neuronal asymmetry in vivo. Nat. Neurosci. 14: 1525– 1533. 10.1038/nn.2976 22081156 · DOI
- Renshaw M.J., Liu J., Lavoie B.D., and Wilde A. 2014 Anillin-dependent organization of septin filaments promotes intercellular bridge elongation and Chmp4B targeting to the abscission site. Open Biol. 4: 130190 10.1098/rsob.130190 24451548 PMC3909275 · DOI
- Ribet D., Boscaini S., Cauvin C., Siguier M., Mostowy S., Echard A., and Cossart P. 2017 SUMOylation of human septins is critical for septin filament bundling and cytokinesis. J. Cell Biol. 216: 4041– 4052. 10.1083/jcb.201703096 29051266 PMC5716278 · DOI
- Roll-Mecak A., and McNally F.J. 2010 Microtubule-severing enzymes. Curr. Opin. Cell Biol. 22: 96– 103. 10.1016/j.ceb.2009.11.001 19963362 PMC2822099 · DOI
- Salzmann V., Chen C., Chiang C.Y., Tiyaboonchai A., Mayer M., and Yamashita Y.M. 2014 Centrosome-dependent asymmetric inheritance of the midbody ring in Drosophila germline stem cell division. Mol. Biol. Cell. 25: 267– 275. 10.1091/mbc.e13-09-0541 24227883 PMC3890347 · DOI
- Schiel J.A., Park K., Morphew M.K., Reid E., Hoenger A., and Prekeris R. 2011 Endocytic membrane fusion and buckling-induced microtubule severing mediate cell abscission. J. Cell Sci. 124: 1411– 1424. 10.1242/jcs.081448 21486954 PMC3078810 · DOI
- Schiel J.A., Simon G.C., Zaharris C., Weisz J., Castle D., Wu C.C., and Prekeris R. 2012 FIP3-endosome-dependent formation of the secondary ingression mediates ESCRT-III recruitment during cytokinesis. Nat. Cell Biol. 14: 1068– 1078. 10.1038/ncb2577 23000966 PMC4495918 · DOI
- Sherman S., Kirchenbuechler D., Nachmias D., Tamir A., Werner S., Elbaum M., and Elia N. 2016 Resolving new ultrastructural features of cytokinetic abscission with soft-X-ray cryo-tomography. Sci. Rep. 6: 27629 10.1038/srep27629 27282220 PMC4901327 · DOI
- Sieg D.J., Hauck C.R., Ilic D., Klingbeil C.K., Schaefer E., Damsky C.H., and Schlaepfer D.D. 2000 FAK integrates growth-factor and integrin signals to promote cell migration. Nat. Cell Biol. 2: 249– 256. 10.1038/35010517 10806474 · DOI
- Singh D., and Pohl C. 2014 Coupling of rotational cortical flow, asymmetric midbody positioning, and spindle rotation mediates dorsoventral axis formation in C. elegans. Dev. Cell. 28: 253– 267. 10.1016/j.devcel.2014.01.002 24525186 · DOI
- Skop A.R., Liu H., Yates J. III, Meyer B.J., and Heald R. 2004 Dissection of the mammalian midbody proteome reveals conserved cytokinesis mechanisms. Science. 305: 61– 66. 10.1126/science.1097931 15166316 PMC3679889 · DOI
- Sorkin A., and von Zastrow M. 2009 Endocytosis and signalling: intertwining molecular networks. Nat. Rev. Mol. Cell Biol. 10: 609– 622. 10.1038/nrm2748 19696798 PMC2895425 · DOI
- Valenstein M.L., and Roll-Mecak A. 2016 Graded Control of Microtubule Severing by Tubulin Glutamylation. Cell. 164: 911– 921. 10.1016/j.cell.2016.01.019 26875866 PMC6459029 · DOI
- Vietri M., Schink K.O., Campsteijn C., Wegner C.S., Schultz S.W., Christ L., Thoresen S.B., Brech A., Raiborg C., and Stenmark H. 2015 Spastin and ESCRT-III coordinate mitotic spindle disassembly and nuclear envelope sealing. Nature. 522: 231– 235. 10.1038/nature14408 26040712 · DOI
- Wang K., Wloka C., and Bi E. 2019 Non-muscle Myosin-II Is Required for the Generation of a Constriction Site for Subsequent Abscission. iScience. 13: 69– 81. 10.1016/j.isci.2019.02.010 30825839 PMC6396101 · DOI
- Wang T., Yanger K., Stanger B.Z., Cassio D., and Bi E. 2014 Cytokinesis defines a spatial landmark for hepatocyte polarization and apical lumen formation. J. Cell Sci. 127: 2483– 2492. 10.1242/jcs.139923 24706948 PMC4038943 · DOI
- White E.A., and Glotzer M. 2012 Centralspindlin: at the heart of cytokinesis. Cytoskeleton (Hoboken). 69: 882– 892. 10.1002/cm.21065 22927365 PMC3821549 · DOI · Paper page
- Yang D., Rismanchi N., Renvoisé B., Lippincott-Schwartz J., Blackstone C., and Hurley J.H. 2008 Structural basis for midbody targeting of spastin by the ESCRT-III protein CHMP1B. Nat. Struct. Mol. Biol. 15: 1278– 1286. 10.1038/nsmb.1512 18997780 PMC2593743 · DOI
- Zheng R., Shen Z.. Tripathi V., Xuan Z., Freier S.M., Bennett C.F., Prasanth S.G., Prasanth K.V. 2010 Polypurine-repeat-containing rnas: a novel class of long non-coding rna in mammalian cells. J. Cell Sci. 123: 3734– 3744. 10.1242/jcs.070466 20940252 PMC4481618 · DOI
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A live-cell marker to visualize the dynamics of stable microtubules throughout the cell cycle
Jansen, K. I., Iwanski, M. K., Burute, M., & Kapitein, L. C. (2023) · Journal of Cell Biology · doi:10.1083/jcb.202106105 · Cited by 39 · see citing works
- Authors
- Peterman, E., & Prekeris, R.
- Affiliations
- University of Colorado Anschutz (US)
- Corresponding author
- Prekeris, Rytis
- Venue
- Journal of Cell Biology
- Publisher
- Rockefeller University Press
- Published
- 2019-11-05
- Volume
- 218
- Issue
- 12
- Pages
- 3903-3911
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- PMC
- PMC6891101
- OpenAlex
- W2987451180
- Cited by
- 60
- References
- 1
- Citations by year
- 2026: 7 · 2025: 9 · 2024: 6 · 2023: 10 · 2022: 16 · 2021: 7 · 2020: 4
- FWCI
- 0.79
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- The Journal of Cell Biology (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion, cc-by-nc-sa)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (DK064380, GM122768)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Microtubule and mitosis dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Keywords
- midbody, abscission, cytokinesis, cell polarity, stemness, cell proliferation, microtubule severing, endosomal trafficking, membrane trafficking, cytoskeletal dynamics, tumorigenicity
- MeSH terms
- Actins, Animals, Cell Division, Cell Membrane, Cytoskeleton, Endocytosis, HeLa Cells, Humans, Microtubules, Mitosis, Spindle Apparatus, Neoplasms, Phagocytes, Endosomes, Stem Cells, Signal Transduction, Cell Polarity, Cell Line, Tumor, Cytokinesis, Cell Proliferation, Endosomal Sorting Complexes Required for Transport
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