Abstract
Swiss 3T3 fibroblasts and LLC-PK epithelial cells in prometaphase or metaphase were either injected with fura-2 or loaded with the acetoxymethyl ester derivative of fura-2 (fura-2 AM) and monitored by microspectrofluorimetry. With both methods of loading, we observed two aspects of intracellular free calcium (Cai) metabolism. (a) Most fibroblasts and epithelial cells exhibited a gradual rise from 75 nM in metaphase to 185 nM during cleavage, returning to baseline by early G1. (b) Mitotic Swiss 3T3 cells exhibited rapid transient Cai changes, similar to those previously reported [Poenie, M., J. Alderton, R. Y. Tsien, R. A. Steinhardt. 1985. Nature (Lond.). 315:147-149; Poenie, M., J. Alderton, R. Steinhardt, and R. Tsien. 1986. Science (Wash. DC). 233:886-889; Ratan, R., and M. L. Shelanski. 1988. J. Cell Biol. 107:993]. These Cai transients occurred repetitively, often beginning in metaphase and continuing long after daughter cell formation. Eliminating serum or calcium from the medium abolished the transients, but delayed neither the gradual Cai elevation nor anaphase onset. Co- injection of EGTA or 1,2-bis-(2-aminophenoxy)-ethane-N,N,N',N'- tetraacetic acid (BAPTA) with fura-2 in calcium-free medium, but not in calcium containing medium, blocked both anaphase and the sustained Cai elevation in almost all cases. Blocked cells were rescued by returning calcium to the medium, whereupon Cai slowly but steadily rose as the cell entered anaphase. Spindle microtubules persisted through the EGTA block. Depolymerization of spindle microtubules by nocodazole also reversibly blocked anaphase onset and the sustained Cai elevation, but did not block transients. This study has revealed the following: (a) anaphase in mammalian fibroblasts and epithelial cells is not triggered by brief calcium transients; (b) anaphase is a calcium-modulated event, usually accompanied by a sustained elevation of Cai above 50 nM; (c) the elevation of Cai is dependent upon an intact spindle; and (d) fibroblasts progress through mitosis by drawing upon either intracellular or extracellular sources of calcium.
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- Alkon D. L., Rasmussen H. A spatial-temporal model of cell activation. Science. 1988 Feb 26;239(4843):998–1005. doi: 10.1126/science.2830669. [DOI] [PubMed] [Google Scholar]
- Andersen B., Osborn M., Weber K. Specific visualization of the distribution of the calcium dependent regulatory protein of cyclic nucleotide phosphodiesterase (modulator protein) in tissue culture cells by immunofluorescence microscopy: mitosis and intercellular bridge. Cytobiologie. 1978 Aug;17(2):354–364. [PubMed] [Google Scholar]
- Baker P. F., Warner A. E. Intracellular calcium and cell cleavage in early embryos of Xenopus laevis. J Cell Biol. 1972 May;53(2):579–581. doi: 10.1083/jcb.53.2.579. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Berridge M. J., Galione A. Cytosolic calcium oscillators. FASEB J. 1988 Dec;2(15):3074–3082. doi: 10.1096/fasebj.2.15.2847949. [DOI] [PubMed] [Google Scholar]
- Carafoli E. Intracellular calcium homeostasis. Annu Rev Biochem. 1987;56:395–433. doi: 10.1146/annurev.bi.56.070187.002143. [DOI] [PubMed] [Google Scholar]
- Chen C. F., Corbley M. J., Roberts T. M., Hess P. Voltage-sensitive calcium channels in normal and transformed 3T3 fibroblasts. Science. 1988 Feb 26;239(4843):1024–1026. doi: 10.1126/science.2449730. [DOI] [PubMed] [Google Scholar]
- Chen T. L., Wolniak S. M. Mitotic progression in stamen hair cells of Tradescantia is accelerated by treatment with ruthenium red and Bay K-8644. Eur J Cell Biol. 1987 Dec;45(1):16–22. [PubMed] [Google Scholar]
- Dinsmore J. H., Sloboda R. D. Calcium and calmodulin-dependent phosphorylation of a 62 kd protein induces microtubule depolymerization in sea urchin mitotic apparatuses. Cell. 1988 Jun 3;53(5):769–780. doi: 10.1016/0092-8674(88)90094-3. [DOI] [PubMed] [Google Scholar]
- Gorbsky G. J., Sammak P. J., Borisy G. G. Chromosomes move poleward in anaphase along stationary microtubules that coordinately disassemble from their kinetochore ends. J Cell Biol. 1987 Jan;104(1):9–18. doi: 10.1083/jcb.104.1.9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gundersen G. G., Kalnoski M. H., Bulinski J. C. Distinct populations of microtubules: tyrosinated and nontyrosinated alpha tubulin are distributed differently in vivo. Cell. 1984 Oct;38(3):779–789. doi: 10.1016/0092-8674(84)90273-3. [DOI] [PubMed] [Google Scholar]
- Hafner M., Petzelt C. Inhibition of mitosis by an antibody to the mitotic calcium transport system. Nature. 1987 Nov 19;330(6145):264–266. doi: 10.1038/330264a0. [DOI] [PubMed] [Google Scholar]
- Hepler P. K. Calcium restriction prolongs metaphase in dividing Tradescantia stamen hair cells. J Cell Biol. 1985 May;100(5):1363–1368. doi: 10.1083/jcb.100.5.1363. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hepler P. K., Callaham D. A. Free calcium increases during anaphase in stamen hair cells of Tradescantia. J Cell Biol. 1987 Nov;105(5):2137–2143. doi: 10.1083/jcb.105.5.2137. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Izant J. G. The role of calcium ions during mitosis. Calcium participates in the anaphase trigger. Chromosoma. 1983;88(1):1–10. doi: 10.1007/BF00329497. [DOI] [PubMed] [Google Scholar]
- Jacob R., Merritt J. E., Hallam T. J., Rink T. J. Repetitive spikes in cytoplasmic calcium evoked by histamine in human endothelial cells. Nature. 1988 Sep 1;335(6185):40–45. doi: 10.1038/335040a0. [DOI] [PubMed] [Google Scholar]
- Keith C. H. Effect of microinjected calcium-calmodulin on mitosis in PtK2 cells. Cell Motil Cytoskeleton. 1987;7(1):1–9. doi: 10.1002/cm.970070102. [DOI] [PubMed] [Google Scholar]
- Kiehart D. P. Studies on the in vivo sensitivity of spindle microtubules to calcium ions and evidence for a vesicular calcium-sequestering system. J Cell Biol. 1981 Mar;88(3):604–617. doi: 10.1083/jcb.88.3.604. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kreis T. E., Birchmeier W. Microinjection of fluorescently labeled proteins into living cells with emphasis on cytoskeletal proteins. Int Rev Cytol. 1982;75:209–214. doi: 10.1016/s0074-7696(08)61005-0. [DOI] [PubMed] [Google Scholar]
- Kruskal B. A., Maxfield F. R. Cytosolic free calcium increases before and oscillates during frustrated phagocytosis in macrophages. J Cell Biol. 1987 Dec;105(6 Pt 1):2685–2693. doi: 10.1083/jcb.105.6.2685. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lee G. M., Diguiseppi J., Gawdi G. M., Herman B. Chloral hydrate disrupts mitosis by increasing intracellular free calcium. J Cell Sci. 1987 Dec;88(Pt 5):603–612. doi: 10.1242/jcs.88.5.603. [DOI] [PubMed] [Google Scholar]
- Malgaroli A., Milani D., Meldolesi J., Pozzan T. Fura-2 measurement of cytosolic free Ca2+ in monolayers and suspensions of various types of animal cells. J Cell Biol. 1987 Nov;105(5):2145–2155. doi: 10.1083/jcb.105.5.2145. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Murray A. W. Cell biology. Cyclins in meiosis and mitosis. Nature. 1987 Apr 9;326(6113):542–543. doi: 10.1038/326542a0. [DOI] [PubMed] [Google Scholar]
- Murray A. W., Kirschner M. W. Cyclin synthesis drives the early embryonic cell cycle. Nature. 1989 May 25;339(6222):275–280. doi: 10.1038/339275a0. [DOI] [PubMed] [Google Scholar]
- Osborn M., Weber K. Immunofluorescence and immunocytochemical procedures with affinity purified antibodies: tubulin-containing structures. Methods Cell Biol. 1982;24:97–132. doi: 10.1016/s0091-679x(08)60650-0. [DOI] [PubMed] [Google Scholar]
- Pandiella A., Malgaroli A., Meldolesi J., Vicentini L. M. EGF raises cytosolic Ca2+ in A431 and Swiss 3T3 cells by a dual mechanism. Redistribution from intracellular stores and stimulated influx. Exp Cell Res. 1987 May;170(1):175–185. doi: 10.1016/0014-4827(87)90127-3. [DOI] [PubMed] [Google Scholar]
- Petzelt C., Hafner M., Mazia D., Sawin K. W. Microtubules and Ca2+-sequestering membranes in the mitotic apparatus, isolated by a new method. Eur J Cell Biol. 1988 Feb;45(2):268–273. [PubMed] [Google Scholar]
- Poenie M., Alderton J., Steinhardt R., Tsien R. Calcium rises abruptly and briefly throughout the cell at the onset of anaphase. Science. 1986 Aug 22;233(4766):886–889. doi: 10.1126/science.3755550. [DOI] [PubMed] [Google Scholar]
- Poenie M., Alderton J., Tsien R. Y., Steinhardt R. A. Changes of free calcium levels with stages of the cell division cycle. Nature. 1985 May 9;315(6015):147–149. doi: 10.1038/315147a0. [DOI] [PubMed] [Google Scholar]
- Ratan R. R., Maxfield F. R., Shelanski M. L. Long-lasting and rapid calcium changes during mitosis. J Cell Biol. 1988 Sep;107(3):993–999. doi: 10.1083/jcb.107.3.993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ratan R. R., Shelanski M. L., Maxfield F. R. Transition from metaphase to anaphase is accompanied by local changes in cytoplasmic free calcium in Pt K2 kidney epithelial cells. Proc Natl Acad Sci U S A. 1986 Jul;83(14):5136–5140. doi: 10.1073/pnas.83.14.5136. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rieder C. L. Effect of hypothermia (20-25 degrees C) on mitosis in PtK1 cells. Cell Biol Int Rep. 1981 Jun;5(6):563–573. doi: 10.1016/s0309-1651(81)80007-0. [DOI] [PubMed] [Google Scholar]
- Rink T. J. A real receptor-operated calcium channel? Nature. 1988 Aug 25;334(6184):649–650. doi: 10.1038/334649a0. [DOI] [PubMed] [Google Scholar]
- Schliwa M., van Blerkom J. Structural interaction of cytoskeletal components. J Cell Biol. 1981 Jul;90(1):222–235. doi: 10.1083/jcb.90.1.222. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schollmeyer J. E. Calpain II involvement in mitosis. Science. 1988 May 13;240(4854):911–913. doi: 10.1126/science.2834825. [DOI] [PubMed] [Google Scholar]
- Silver R. B. Mitosis in sand dollar embryos is inhibited by antibodies directed against the calcium transport enzyme of muscle. Proc Natl Acad Sci U S A. 1986 Jun;83(12):4302–4306. doi: 10.1073/pnas.83.12.4302. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vandre D. D., Davis F. M., Rao P. N., Borisy G. G. Phosphoproteins are components of mitotic microtubule organizing centers. Proc Natl Acad Sci U S A. 1984 Jul;81(14):4439–4443. doi: 10.1073/pnas.81.14.4439. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Weisenberg R. C., Deery W. J. The mechanism of calcium-induced microtubule disassembly. Biochem Biophys Res Commun. 1981 Oct 15;102(3):924–931. doi: 10.1016/0006-291x(81)91626-0. [DOI] [PubMed] [Google Scholar]
- Weisenberg R. C. Microtubule formation in vitro in solutions containing low calcium concentrations. Science. 1972 Sep 22;177(4054):1104–1105. doi: 10.1126/science.177.4054.1104. [DOI] [PubMed] [Google Scholar]
- Welsh M. J., Dedman J. R., Brinkley B. R., Means A. R. Tubulin and calmodulin. Effects of microtubule and microfilament inhibitors on localization in the mitotic apparatus. J Cell Biol. 1979 Jun;81(3):624–634. doi: 10.1083/jcb.81.3.624. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wolniak S. M., Bart K. M. Nifedipine reversibly arrests mitosis in stamen hair cells of tradescantia. Eur J Cell Biol. 1986 Jan;39(2):273–277. [PubMed] [Google Scholar]
- Wolniak S. M., Bart K. M. The buffering of calcium with quin2 reversibly forestalls anaphase onset in stamen hair cells of Tradescantia. Eur J Cell Biol. 1985 Nov;39(1):33–40. [PubMed] [Google Scholar]
- Woods N. M., Cuthbertson K. S., Cobbold P. H. Repetitive transient rises in cytoplasmic free calcium in hormone-stimulated hepatocytes. Nature. 1986 Feb 13;319(6054):600–602. doi: 10.1038/319600a0. [DOI] [PubMed] [Google Scholar]
- Zavortink M., Welsh M. J., McIntosh J. R. The distribution of calmodulin in living mitotic cells. Exp Cell Res. 1983 Dec;149(2):375–385. doi: 10.1016/0014-4827(83)90350-6. [DOI] [PubMed] [Google Scholar]
- Ziegler M. L., Sisken J. E., Vedbrat S. The alteration of mitotic events by ionophore A23187 and carbonyl cyanide n-chlorophenylhydrazone. J Cell Sci. 1985 Apr;75:347–355. doi: 10.1242/jcs.75.1.347. [DOI] [PubMed] [Google Scholar]