Skip to main content

Ca2+ Signalling and Membrane Dynamics During Cytokinesis in Animal Cells

  • Chapter
  • First Online:
Membrane Dynamics and Calcium Signaling

Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 981))

Abstract

Interest in the role of Ca2+ signalling as a possible regulator of the combinatorial processes that result in the separation of the daughter cells during cytokinesis, extend back almost a 100 years. One of the key processes required for the successful completion of cytokinesis in animal cells (especially in the large holoblastically and meroblastically dividing embryonic cells of a number of amphibian and fish species), is the dynamic remodelling of the plasma membrane. Ca2+ signalling was subsequently demonstrated to regulate various different aspects of cytokinesis in animal cells, and so here we focus specifically on the role of Ca2+ signalling in the remodelling of the plasma membrane. We begin by providing a brief history of the animal models used and the research accomplished by the early twentieth century investigators, with regards to this aspect of animal cell cytokinesis. We then review the most recent progress made (i.e., in the last 10 years), which has significantly advanced our current understanding on the role of cytokinetic Ca2+ signalling in membrane remodelling. To this end, we initially summarize what is currently known about the Ca2+ transients generated during animal cell cytokinesis, and then we describe the latest findings regarding the source of Ca2+ generating these transients. Finally, we review the current evidence about the possible targets of the different cytokinetic Ca2+ transients with a particular emphasis on those that either directly or indirectly affect plasma membrane dynamics. With regards to the latter, we discuss the possible role of the early Ca2+ signalling events in the deformation of the plasma membrane at the start of cytokinesis (i.e., during furrow positioning), as well as the role of the subsequent Ca2+ signals in the trafficking and fusion of vesicles, which help to remodel the plasma membrane during the final stages of cell division. As it is becoming clear that each of the cytokinetic Ca2+ transients might have multiple, integrated targets, deciphering the precise role of each transient represents a significant (and ongoing) challenge.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 109.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 139.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 199.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. Atilla-Gokcumen GE, Castoreno AB, Sasse S, Eggert US (2010) Making the cut: the chemical biology of cytokinesis. ACS Chem Biol 5:79–90

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  2. Barr FA, Gruneberg U (2007) Cytokinesis: placing and making the final cut. Cell 131:847–860

    Article  CAS  PubMed  Google Scholar 

  3. Green RA, Paluch E, Oegema K (2012) Cytokinesis in animal cells. Ann Rev Cell Dev Biol 28:29–58

    Article  CAS  Google Scholar 

  4. McMichael CM, Bednarek SY (2013) Cytoskeletal and membrane dynamics during higher plant cytokinesis. New Phytol 197:1039–1057

    Article  CAS  PubMed  Google Scholar 

  5. Oliferenko S, Chew TG, Balasubramanian MK (2009) Positioning cytokinesis. Genes Dev 23:660–674

    Article  CAS  PubMed  Google Scholar 

  6. Pollard TD (2010) Mechanics of cytokinesis in eukaryotes. Curr Opin Cell Biol 22:50–56

    Article  CAS  PubMed  Google Scholar 

  7. Dan K, Dan JC (1940) Behavior of the cell surface during cleavage III. On the formation of new surface in the eggs of Strongylocentrotus pulcherrimus. Biol Bull 78:486–501

    Article  Google Scholar 

  8. Dan K, Yanagita T, Sugiyama M (1937) Behavior of the cell surface during cleavage I. Protoplasma 28:66–81

    Article  CAS  Google Scholar 

  9. Motomura I (1940) Studies of cleavage I. Changes in the surface area of different regions of eggs of a sea urchin in the course of the first cleavage. Sci Rep Tôhoku Imp Univ Ser 4 15:121–130

    Google Scholar 

  10. Rappaport R, Ratner JH (1967) Cleavage of sand dollar eggs with altered patterns of new surface formation. J Exp Zool 165:89–100

    Article  Google Scholar 

  11. Tilney LG, Marsland D (1969) A fine structural analysis of cleavage induction and furrowing in the eggs of Arbacia punctulata. J Cell Biol 42:170–184

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  12. Gray J (1924) The mechanism of cell-division I. The forces which control the form and cleavage of the eggs of Echinus esculentus. Biol Rev 1:164–188

    Article  Google Scholar 

  13. Motomura I (1941) Studies of cleavage II. Cleavage of the cells of a sea urchin, Strongylocentrotus pulcherrimus, in calcium-free sea water. Sci Rep Tôhoku Imp Univ, Ser 4 16:283–290

    Google Scholar 

  14. Dan K (1954) Further study on the formation of the “new membrane” in the eggs of the sea urchin, Hemicentrotus (Strongylocentrotus) pulcherrimus. Embryologia 2:99–113

    Article  Google Scholar 

  15. Selman GG, Perry MM (1970) Ultrastructural changes in the surface layers of the newt’s egg in relation to the mechanism of its cleavage. J Cell Sci 6:207–227

    CAS  PubMed  Google Scholar 

  16. Selman GG, Waddington CH (1955) The mechanism of cell division in the cleavage of the newt’s egg. J Exp Biol 32:700–733

    Google Scholar 

  17. Dan K, Kuno Kojima M (1963) A study on the mechanism of cleavage in the amphibian egg. J Exp Biol 40:7–14

    Google Scholar 

  18. Sawai T (1976) Movement of the cell surface and change in surface area during cleavage in the newt’s egg. J Cell Sci 21:537–551

    CAS  PubMed  Google Scholar 

  19. Sawai T (1987) Surface movement in the region of the cleavage furrow of amphibian eggs. Zool Sci (Tokyo) 4:825–832

    Google Scholar 

  20. Woodward DJ (1968) Electrical signs of new membrane production during cleavage of Rana pipiens eggs. J Gen Physiol 52:509–531

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  21. Bluemink JG, de Latt SW (1973) New membrane formation during cytokinesis in normal and cytochalasin B-treated eggs of Xenopus laevis I. Electron microscope observations. J Cell Biol 59:89–108

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  22. Byers TJ, Armstrong PB (1986) Membrane protein redistribution during Xenopus first cleavage. J Cell Biol 102:2176–2184

    Article  CAS  PubMed  Google Scholar 

  23. Li WM, Webb SE, Lee KW, Miller AL (2006) Recruitment and SNARE-mediated fusion of vesicles in furrow membrane remodeling during cytokinesis in zebrafish embryos. Exp Cell Res 312:3260–3275

    Article  CAS  PubMed  Google Scholar 

  24. Fluck RA, Miller AL, Jaffe LA (1991) Slow calcium waves accompany cytokinesis in medaka fish eggs. J Cell Biol 115:1259–1265

    Article  CAS  PubMed  Google Scholar 

  25. Lecuit T, Wieschaus E (2000) Polarized insertion of new membrane from a cytoplasmic reservoir during cleavage of Drosophila embryo. J Cell Biol 150:849–860

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  26. Takeda T, Robinson IM, Savoian MM, Griffiths JR, Whetton AD, McMahon HT, Glover DM (2013) Drosophila F-BAR protein Syndapin contributes to coupling the plasma membrane and contractile ring in cytokinesis. Open Biol 3:130081. https://doi.org/10.1098/rsob.130081

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  27. Skop AR, Bergmann D, Mohler WA, White JG (2001) Completion of cytokinesis in C. elegans requires a brefeldin A-sensitive membrane accumulation at the cleavage furrow apex. Curr Biol 11:735–746

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  28. Rappaport R (1996) Cytokinesis in animal cells. Developmental and cell biology series. Cambridge University Press, Cambridge, UK

    Book  Google Scholar 

  29. Albertson R, Riggs B, Sullivan W (2005) Membrane traffic: a driving force in cytokinesis. Trends Cell Biol 15:92–101

    Article  CAS  PubMed  Google Scholar 

  30. Straight AF, Field CM (2000) Microtubules, membranes and cytokinesis. Curr Biol 10:R760–RR70

    Article  CAS  PubMed  Google Scholar 

  31. Dan K (1988) Mechanism of equal cleavage of sea urchin egg: transposition from astral mechanism to constricting mechanism. Zool Sci 5:507–517

    Google Scholar 

  32. Schroeder TE (1972) The contractile ring. II Determining its brief existence, volumetric changes, and vital role in cleaving Arbacia eggs. J Cell Biol 53:419–434

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  33. Li WM, Webb SE, Chan CM, Miller AL (2008) Multiple roles of the furrow deepening Ca2+ transient during cytokinesis in zebrafish embryos. Dev Biol 316:228–248

    Article  CAS  PubMed  Google Scholar 

  34. Lee KW, Ho SM, Wong CH, Webb SE, Miller AL (2004) Characterization of mid-spindle microtubules during furrow positioning in early cleavage period zebrafish embryos. Zygote 12:221–230

    Article  CAS  PubMed  Google Scholar 

  35. Lee KW, Webb SE, Miller AL (2006) Requirement for a localized, IP3R-generated Ca2+ transient during the furrow positioning process in zebrafish zygotes. Zygote 14:143–155

    Article  CAS  PubMed  Google Scholar 

  36. Webb SE, Lee KW, Karplus E, Miller AL (1997) Localized calcium transients accompany furrow positioning, propagation, and deepening during the early cleavage period of zebrafish embryos. Dev Biol 192:78–92

    Article  CAS  PubMed  Google Scholar 

  37. Lee KW, Webb SE, Miller AL (2003) Ca2+ released via IP3 receptors is required for furrow deepening during cytokinesis in zebrafish eggs. Int J Dev Biol 47:411–421

    CAS  PubMed  Google Scholar 

  38. Guertin DA, Trautmann S, McCollum D (2002) Cytokinesis in eukaryotes. Microbiol Mol Biol Rev 66:155–178

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  39. Guizetti J, Gerlich DW (2010) Cytokinetic abscission in animal cells. Sem Cell Dev Biol 21:909–916

    Article  CAS  Google Scholar 

  40. Rothfield LI, Justice SS (1997) Bacterial cell division: the cycle of the ring. Cell 88:581–584

    Article  CAS  PubMed  Google Scholar 

  41. Yeong FM (2005) Severing all ties between mother and daughter: cell separation in budding yeast. Mol Micro 55:1325–1331

    Article  CAS  Google Scholar 

  42. Danilchik MV, Brown EE (2008) Membrane dynamics of cleavage furrow closure in Xenopus laevis. Dev Dyn 237:565–579

    Article  PubMed  Google Scholar 

  43. Jesuthasan S (1998) Furrow-associated microtubule arrays are required for the cohesion of zebrafish blastomeres following cytokinesis. J Cell Sci 111:3695–3703

    CAS  PubMed  Google Scholar 

  44. Muto A, Kume S, Inoue T, Okano H, Mikoshiba K (1996) Calcium waves along the cleavage furrows in cleavage-stage Xenopus embryos and its inhibition by heparin. J Cell Biol 135:181–190

    Article  CAS  PubMed  Google Scholar 

  45. Webb SE, Miller AL (2007) Ca2+ signaling during embryonic cytokinesis in animal systems. In: Krebs J, Michalak M (eds) Calcium: a matter of life and death. Elsevier, B.V., Amsterdam, The Netherlands, pp 445–470. https://doi.org/10.1016/S0167-7306(06)41017-6

    Chapter  Google Scholar 

  46. Aimar C (1997) Formation of new plasma membrane during the first cleavage cycle in the eggs of Xenopus laevis: an immunocytological study. Dev Growth Dev 39:693–704

    Article  CAS  Google Scholar 

  47. Danilchik MV, Funk WC, Brown EE, Larkin K (1998) Requirement for microtubules in new membrane formation during cytokinesis of Xenopus embryos. Dev Biol 194:47–60

    Article  CAS  PubMed  Google Scholar 

  48. Shuster CB, Burgess DR (2002) Targeted new membrane addition in the cleavage furrow is a late, separate event in cytokinesis. Proc Natl Acad Sci USA 99:3633–3638

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  49. Finger FP, White JG (2002) Fusion and fission: membrane trafficking in animal cells. Cell 108:727–730

    Article  CAS  PubMed  Google Scholar 

  50. Schiel JA, Prekeris R (2013) Membrane dynamics during cytokinesis. Curr Opin Cell Biol 25:92–98

    Article  CAS  PubMed  Google Scholar 

  51. Bezanilla M, Gladfelter AS, Kovar DR (2015) Cytoskeletal dynamics: a view from the membrane. J Cell Biol 209:329–337

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  52. Heng YW, Koh CG (2010) Actin cytoskeleton dynamics and the cell division cycle. Int J Biochem Cell Biol 42:1622–1633

    Article  CAS  PubMed  Google Scholar 

  53. Miller AL, Fluck RA, MccLaughlin JA, Jaffe LF (1993) Calcium buffer injections inhibit cytokinesis in Xenopus eggs. J Cell Sci 106:523–534

    CAS  PubMed  Google Scholar 

  54. Simon GC, Prekeris R (2008) Mechanisms regulating targeting of recycling endosomes to the cleavage furrow during cytokinesis. Biochem Soc Trans 36:391–394

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  55. Arnold JM (1975) An effect of calcium in cytokinesis as demonstrated with ionophore A 23187. Cytobiologie 11:1–9

    CAS  Google Scholar 

  56. Baker PF, Warner AE (1972) Intracellular calcium and cell cleavage in early embryos of Xenopus laevis. J Cell Biol 53:579–581

    Article  PubMed Central  PubMed  Google Scholar 

  57. Ridgway EB, Gilkey JC, Jaffe LF (1977) Free calcium increases explosively in activating medaka eggs. Proc Natl Acad Sci USA 74:623–627

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  58. Schroeder TE, Strickland DL (1974) Ionophore A23187, calcium and contractility in frog eggs. Exp Cell Res 83:139–142

    Article  CAS  PubMed  Google Scholar 

  59. Chang DC, Meng C (1995) A localized elevation of cytosolic free calcium is associated with cytokinesis in the zebrafish embryo. J Cell Biol 131:1539–1545

    Article  CAS  PubMed  Google Scholar 

  60. Créton R, Speksnijder JE, Jaffe LF (1998) Patterns of free calcium in zebrafish embryos. J Cell Sci 111:1613–1622

    PubMed  Google Scholar 

  61. Shantz AR (1985) Cytosolic free calcium-ion concentration in cleaving embryonic cells of Oryzias latipes measured with calcium-selective microelectrodes. J Cell Biol 100:947–954

    Article  Google Scholar 

  62. Miller AL, Karplus E, Jaffe LF (1994) Use of aequorin for [Ca2+]i imaging. Chapter 13. In: Nuccitelli R (ed) Methods in cell biology, Vol 40: a practical guide to the study of Ca2+ in living cells. Academic press, San Diego, pp 305–338

    Chapter  Google Scholar 

  63. Chang DC, Lu P (2000) Multiple types of calcium signals are associated with cell division in zebrafish embryo. Micros Res Tech 49:111–122

    Article  CAS  Google Scholar 

  64. Guo YB, Wen Y, Gao WX, Li JC, Zhou P, Bai ZL, Zhang B, Wang SQ (2010) The formation of Ca2+ gradients at the cleavage furrows during cytokinesis of zebrafish embryos. Front Biol 5:369–377

    Article  CAS  Google Scholar 

  65. Chen J, Xia L, Bruchas MR, Solnica-Krezel L (2017) Imaging early embryonic calcium activity with GCaMP6s transgenic zebrafish. Dev Biol 430(2):385–396

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  66. Stricker SA (1995) Time-lapse confocal imaging of calcium dynamics in starfish embryos. Dev Biol 170:496–518

    Article  CAS  PubMed  Google Scholar 

  67. Silver RB (1996) Calcium, BOBs, QEDs, microdomains and a cellular decision: control of mitotic cell division in sand dollar blastomeres. Cell Calc 20:161–179

    Article  CAS  Google Scholar 

  68. Ciapa B, Pesando D, Wilding M, Whitaker M (1994) Cell-cycle calcium transients driven by cyclic changes in inositol trisphosphate levels. Nature 368:875–878

    Article  CAS  PubMed  Google Scholar 

  69. Peonie M, Alderton J, Tsien RY, Steinhardt RA (1985) Changes of free calcium levels with stages of the cell division cycle. Nature 315:147–149

    Article  Google Scholar 

  70. Liu X, Wang P, Fu J, Lv D, Chen D, Li Y, Ma W (2011) Two-photon fluorescence real-time imaging on the development of early mouse embryo by stages. J Microsc 241:212–218

    Article  CAS  PubMed  Google Scholar 

  71. Mitsuyama F, Sawai T, Carafoli E, Furuichi T, Mikoshiba K (1999) Microinjection of Ca2+ store-enriched microsome fractions to dividing newt eggs induces extra-cleavage furrows via inositol 1,4,5- trisphosphate-induced Ca2+ release. Dev Biol 214:160–167

    Article  CAS  PubMed  Google Scholar 

  72. Mitsuyama F, Sawai T (2001) The redistribution of Ca2+ stores with inositol 1,4,5-trisphosphate receptor to the cleavage furrow in a microtubule-dependent manner. Int J Dev Biol 45:861–868

    CAS  PubMed  Google Scholar 

  73. Mitsuyama F, Futatsugi Y, Okuya M, Karagiozov K, Kato Y, Kanno T, Sano H, Koide T, Sawai T (2008) Microinjected F-actin into dividing newt eggs moves toward the next cleavage furrow together with Ca2+ stores with inositol 1,4,5-trisphosphate receptor in a microtubule- and microtubule motor- dependent manner. It J Anat Embryol 113:143–152

    Google Scholar 

  74. Lee KW, Baker R, Galione A, Gilland EH, Miller AL (1996) Ionophore-induced calcium waves activate unfertilized zebrafish (Danio rerio) eggs. Biol Bull 191:265–267

    Google Scholar 

  75. Kühtreiber WM, Jaffe LF (1990) Detection of extracellular calcium gradients with a calcium-specific vibrating electrode. J Cell Biol 110:1565–1573

    Article  PubMed  Google Scholar 

  76. Chan CM, Chen Y, Hung TS, Miller AL, Shipley AM, Webb SE (2015) Inhibition of SOCE disrupts cytokinesis in zebrafish embryos mainly via inhibition of cleavage furrow deepening. Int J Dev Biol 59:289–301

    Article  CAS  PubMed  Google Scholar 

  77. Chan CM, Aw JTM, Webb SE, Miller AL (2016) SOCE proteins, STIM1 and Orai1, are localized to the cleavage furrow during cytokinesis of the first and second cell division cycles in zebrafish embryos. Zygote 24:880–889

    Article  CAS  PubMed  Google Scholar 

  78. Bomben VC, Sontheimer H (2010) Disruption of transient receptor potential canonical channel 1 causes incomplete cytokinesis and slows the growth of human malignant gliomas. Glia 58:1145–1156

    Article  PubMed Central  PubMed  Google Scholar 

  79. Mabuchu I, Takano-Ohmuro H (1990) Effects of inhibitors of myosin light chain kinase and other protein kinases of the first cell division of sea urchin eggs. Develop Growth Differ 32:549–556

    Article  Google Scholar 

  80. Mabuchu I, Tsukita S, Tsukita S, Sawai T (1988) Cleavage furrow isolated from newt eggs: contraction, organization of the actin filaments, and protein components of the furrow. Proc Natl Acad Sci USA 85:5966–5970

    Article  Google Scholar 

  81. Murthy K, Wadsworth R (2005) Myosin-II-dependent localization and dynamics of F-actin during cytokinesis. Curr Biol 15:724–731

    Article  CAS  PubMed  Google Scholar 

  82. Smith JL, Silveira LA, Spudich JA (1996) Myosin light chain kinase (MLCK) gene disruption in Dictyostelium: a role for MLCK-A in cytokinesis and evidence for multiple MLCKs. Proc Natl Acad Sci USA 93:12321–12326

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  83. Yamakita Y, Yamashiro S, Matsumura F (1994) In vivo phosphorylation of regulatory light chain of myosin II during mitosis of cultured cells. J Cell Biol 124:129–137

    Article  CAS  PubMed  Google Scholar 

  84. Wong R, Fabian L, Forer A, Brill JA (2007) Phospholipase C and myosin light chain kinase inhibition define a common step in actin regulation during cytokinesis. BMC Cell Biol 8:15. https://doi.org/10.1186/1471-2121-8-15

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  85. Wu Q, Sahasrabudhe RM, Luo LZ, Lewis DW, Gollin SM, Saunders WS (2010) Deficiency in myosin light-chain phosphorylation causes cytokinesis failure and multipolarity in cancer cells. Oncogene 29:4183–4193

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  86. Batchelder EL, Thomas-Virnig CL, Hardin JD, White JG (2007) Cytokinesis is not controlled by calmodulin or myosin light chain kinase in the Caenorhabditis elegans early embryo. FEBS Lett 581:4337–4341

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  87. Webb SE, Goulet C, Chan CM, Yuen MYF, Miller AL (2014) Biphasic assembly of the contractile apparatus during the first two cell division cycles in zebrafish embryos. Zygote 22:218–228

    Article  CAS  PubMed  Google Scholar 

  88. Celton-Morizur S, Bordes N, Fraisier V, Tran PT, Paoletti A (2004) C-terminal anchoring of mid1p to the membrane stabilizes cytokinetic ring position in early mitosis in fission yeast. Mol Cell Biol 24:10621–10635

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  89. Laplante C, Huang F, Tebbs IR, Bewersdorf J, Pollard TD (2016) Molecular organization of cytokinesis nodes and contractile rings by super-resolution fluorescence microscopy of live fission yeast. Proc Natl Acad Sci USA 113(40):E5876–E5885. https://doi.org/10.1073/pnas.1608252113

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  90. Field SJ, Madson N, Kerr ML, Galbraith KAA, Kennedy CE, Tahiliani M, Wilkins A, Cantley LC (2005) PtdIns(4,5)P2 functions at the cleavage furrow during cytokinesis. Curr Biol 15:1407–1412

    Article  CAS  PubMed  Google Scholar 

  91. Naito Y, Okada M, Yagisawa H (2006) Phospholipase C isoforms are localised at the cleavage furrow during cytokinesis. J Biochem 140:785–791

    Article  CAS  PubMed  Google Scholar 

  92. Han JK, Fukami K, Nuccitelli R (1992) Reducing inositol lipid hydrolysis, Ins(1,4,5)P3 receptor availability, or Ca2+ gradients lengthens the duration of the cell cycle in Xenopus laevis blastomeres. J Cell Biol 116:147–156

    Article  CAS  PubMed  Google Scholar 

  93. Wong R, Hadjiyanni I, Wei HC, Polevoy G, McBride R, Sem KP, Brill JA (2005) PIP2 hydrolysis and calcium release are required for cytokinesis in Drosophila spermatocytes. Curr Biol 15:1401–1406

    Article  CAS  PubMed  Google Scholar 

  94. Liu J, Fairn GD, Ceccarelli DF, Sicheri F, Wilde A (2012) Cleavage furrow organization requires PIP2- mediated recruitment of anillin. Curr Biol 22:64–69

    Article  CAS  PubMed  Google Scholar 

  95. Piekny AJ, Glotzer M (2007) Anillin is a scaffold protein that links RhoA, actin and myosin during cytokinesis. Curr Biol 18:30–36

    Article  CAS  PubMed  Google Scholar 

  96. Goldback P, Wong R, Beise N, Sarpal R, Trimble WS, Brill JA (2010) Stabilization of the actomyosin ring enables spermatocyte cytokinesis in Drosophila. Mol Biol Cell 21:1482–1493

    Article  CAS  Google Scholar 

  97. Rodal AA, Kozubowski L, Goode BL, Drubin DG, Hartwig JH (2005) Actin and septin ultrastructures at the budding yeast cell cortex. Mol Biol Cell 16:372–384

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  98. Foe VE, Field CM, Odell GM (2000) Microtubules and mitotic cycle phase modulate spatiotemporal distributions of F-actin and myosin II in Drosophila syncytial blastoderm embryos. Development 127:1767–1787

    CAS  PubMed  Google Scholar 

  99. Lucero A, Stack C, Bresnick AR, Shuster CB (2006) A global, myosin light chain kinase-dependent increase in myosin II contractility accompanies the metaphase-anaphase transition in sea urchin eggs. Mol Biol Cell 17:4093–4104

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  100. Li CJ, Heim R, Lu P, Pu Y, Tsien RY, Chang DC (1999) Dynamic redistribution of calmodulin in HeLa cells during cell division as revealed by a GFP-calmodulin fusion protein technique. J Cell Sci 112:1567–1577

    CAS  PubMed  Google Scholar 

  101. Yu YY, Chen Y, Dai G, Chen J, Sun XM, Wen CJ, Zhao DH, Chang DC, Li CJ (2004) The association of calmodulin with central spindle regulates the initiation of cytokinesis in HeLa cells. Int J Biochem Cell Biol 36:1562–1572

    Article  CAS  PubMed  Google Scholar 

  102. Murakoshi H, Wang H, Yasuda R (2011) Local, persistent activation of Rho GTPases during plasticity of single dendritic spines. Nature 472:100–104

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  103. Drechsel DN, Hyman AA, Hall A, Glotzer M (1997) A requirement for Rho and Cdc42 during cytokinesis in Xenopus embryos. Curr Biol 7:12–23

    Article  CAS  PubMed  Google Scholar 

  104. Bernaud C, Le Dez G, Mironov S, Galli F, Reboutier D, Prigent C (2015) Annexin A2 is required for the early steps of cytokinesis. EMBO Rep 16:481–489

    Article  CAS  Google Scholar 

  105. Feng B, Schwarz H, Jesuthasan S (2002) Furrow-specific endocytosis during cytokinesis of zebrafish blastomeres. Exp Cell Res 279:14–20

    Article  CAS  PubMed  Google Scholar 

  106. Caswell PT, Vadrevu S, Norman JC (2009) Integrins: masters and slaves of endocytic transport. Nature Rev Mol Cell Biol 10:843–853

    Article  CAS  Google Scholar 

  107. McKay HF, Burgess DR (2011) ‘Life is a highway’: membrane trafficking during cytokinesis. Traffic 12:247–251

    Article  CAS  PubMed  Google Scholar 

  108. Neto H, Collins LL, Gould GW (2011) Vesicle trafficking and membrane remodeling in cytokinesis. Biochem J 437:13–24

    Article  CAS  PubMed  Google Scholar 

  109. Urven LE, Yabe T, Pelegri F (2006) A role for non-muscle myosin II function in furrow maturation in the early zebrafish embryo. J Cell Sci 119:4342–4352

    Article  CAS  PubMed  Google Scholar 

  110. Sato K, Kawashima S (2001) Calpain function in the modulation of signal transduction molecules. Biol Chem 382:743–751

    Article  CAS  PubMed  Google Scholar 

  111. Chen MC, Zhou Y, Detrich HW III (2002) Zebrafish mitotic kinesin-like protein 1 (Mklp1) functions in embryonic cytokinesis. Physiol Gen 8:51–66

    Article  CAS  Google Scholar 

  112. Raich WB, Moran AN, Rothman JH, Hardin J (1998) Cytokinesis and midzone microtubule organization in Caenorhabditis elegans require the kinesin-like protein ZEN-4. Mol Biol Cell 9:2037–2049

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  113. Kuryama R, Gustus C, Terada Y, Uetake Y, Matuliene J (2002) CHO1, a mammalian kinesin-like protein, interacts with F-actin and is involved in the terminal phase of cytokinesis. J Cell Biol 156:783–790

    Article  CAS  Google Scholar 

  114. Matuliene J, Kuriyama R (2002) Kinesin-like protein CHO1 is required for the formation of midbody matrix and the completion of cytokinesis in mammalian cells. Mol Biol Cell 13:1832–1845

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  115. Zhu C, Bossy-Wetzel E, Jiang W (2005) Recruitment of MKLP1 to the spindle midzone/midbody by INCENP is essential for midbody formation and completion of cytokinesis in human cells. Biochem J 389:373–381

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  116. Abe H, Obinata T, Minamide LS, Bamburg JR (1996) Xenopus laevis actin-depolarizing factor/cofilin: a phosphorylation-regulated protein essential for development. J Cell Biol 132:871–885

    Article  CAS  PubMed  Google Scholar 

  117. Ono K, Parast M, Alberico C, Benian GM, Ono S (2003) Specific requirement for two ADF/cofilin isoforms in distinct actin-dependent processes in Caenorhabditis elegans. J Cell Sci 116:2073–2085

    Article  CAS  PubMed  Google Scholar 

  118. Nusco GA, Chun JT, Ercolano E, Lim D, Gragnaniello G, Kyozuka K, Santella L (2006) Modulation of calcium signalling by the actin-binding protein cofilin. Biochem Biophys Res Communs 348:109–114

    Article  CAS  Google Scholar 

  119. Creutz CE, Tomsig JL, Snyder SL, Gautier MC, Skouri F, Beisson J, Cohen J (1998) The copines, a novel class of C2 domain-containing, calcium-dependent, phospholipid-binding proteins conserved from Paramecium to humans. J Biol Chem 273:1393–1402

    Article  CAS  PubMed  Google Scholar 

  120. Damer CK, Bayeva M, Kim PS, Ho LK, Eberhardt ES, Socec CI, Lee JS, Bruce EA, Goldman-Yassen AE, Naliboff LC (2007) Copine A is required for cytokinesis, contractile vacuole function, and development in Dictyostelium. Euk Cell 6:430–442

    Article  CAS  Google Scholar 

  121. Berridge MJ, Bootman MD, Llewelyn Roderick H (2003) Calcium signalling: dynamics, homeostasis and remodelling. Nature Rev Mol Cell Biol 4:517–529

    Article  CAS  Google Scholar 

Download references

Acknowledgments

We acknowledge funding support from Hong Kong Research Grants Council (RGC) General Research Fund awards 662113, 16101714 and 16100115; the ANR/RGC joint research scheme award A-HKUST601/13 and the Hong Kong Theme-based Research Scheme award T13-706/11-1. We also acknowledge funding support from the Hong Kong Innovation and Technology Commission (ITCPD/17-9).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Andrew L. Miller .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2017 Springer International Publishing AG, part of Springer Nature

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Webb, S.E., Miller, A.L. (2017). Ca2+ Signalling and Membrane Dynamics During Cytokinesis in Animal Cells. In: Krebs, J. (eds) Membrane Dynamics and Calcium Signaling. Advances in Experimental Medicine and Biology, vol 981. Springer, Cham. https://doi.org/10.1007/978-3-319-55858-5_15

Download citation

Publish with us

Policies and ethics