Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1980 Aug 1;86(2):355–365. doi: 10.1083/jcb.86.2.355

Calcium-labile mitotic spindles isolated from sea urchin eggs (Lytechinus variegatus)

PMCID: PMC2111485  PMID: 7190569

Abstract

We isolated calcium-labile mitotic spindles from eggs of the sea urchin Lytechinus variegatus, using a low ionic strength, EGTA lysis buffer that contined 5.0 mM EGTA, 0.5 mM MgCl2, 10-50 mM PIPES, pH 6.8, with 1% Nonidet P-40 (detergent) and 20-25% glycerol. Isolated spindles were stored in EGTA buffer with 50% glycerol for 5-6 wk without deterioration. The isolated spindles were composed primarily of microtubules with the chromosomes attached. No membranes were seen. Isolated spindles, perfused with EGTA buffer to remove the detergent and glycerol, had essentially the same birefringent retardation (BR) as spindles in vivo at the same mitotic stage. Even in the absence of glycerol and exogenous tubulin, the isolated spindles were relatively stable in the EGTA buffer: BR decayed slowly to about half the initial value within 30-45 min. However, both the rate and extent of BR decay increased with concentrations of Ca2+ above 0.2-0.5 muM as assayed using Ca-EGTA buffers (0.2 mM EGTA, 0.5 mM MgCl2, 50 mM PIPES, pH 6.8, plus various amounts of CaCl2). Microtubules depolymerized almost completely in < 6 min at Ca2+ concentrations of 2 muM and within several seconds at 10 muM Ca2+. Of several divalent cations tested, only Sr2+ caused comparable changes in BR. The absence of membranes in the isolated spindles appeared to be associated with a lack of calcium- sequestering ability. Our results suggest that calcium ions play an important role in the depolymerization of spindle microtubules and that membrane components may function within the mitotic apparatus of living cells to sequester and release calcium ions during mitosis.

Full Text

The Full Text of this article is available as a PDF (1.3 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. 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]
  2. Baur P. S., Stacey T. R. The use of PIPES buffer in the fixation of mammalian and marine tissues for electron microscopy. J Microsc. 1977 Apr;109(3):315–327. doi: 10.1111/j.1365-2818.1977.tb01145.x. [DOI] [PubMed] [Google Scholar]
  3. Borisy G. G., Olmsted J. B., Marcum J. M., Allen C. Microtubule assembly in vitro. Fed Proc. 1974 Feb;33(2):167–174. [PubMed] [Google Scholar]
  4. Brinkley B. R., Cartwright J., Jr Cold-labile and cold-stable microtubules in the mitotic spindle of mammalian cells. Ann N Y Acad Sci. 1975 Jun 30;253:428–439. doi: 10.1111/j.1749-6632.1975.tb19218.x. [DOI] [PubMed] [Google Scholar]
  5. Cande W. Z., Snyder J., Smith D., Summers K., McIntosh J. R. A functional mitotic spindle prepared from mammalian cells in culture. Proc Natl Acad Sci U S A. 1974 Apr;71(4):1559–1563. doi: 10.1073/pnas.71.4.1559. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Caswell A. H. Methods of measuring intracellular calcium. Int Rev Cytol. 1979;56:145–181. doi: 10.1016/s0074-7696(08)61822-7. [DOI] [PubMed] [Google Scholar]
  7. Fuller G. M., Brinkley B. R. Structure and control of assembly of cytoplasmic microtubules in normal and transformed cells. J Supramol Struct. 1976;5(4):497(349)–514(366). doi: 10.1002/jss.400050407. [DOI] [PubMed] [Google Scholar]
  8. Gaskin F., Cantor C. R., Shelanski M. L. Turbidimetric studies of the in vitro assembly and disassembly of porcine neurotubules. J Mol Biol. 1974 Nov 15;89(4):737–755. doi: 10.1016/0022-2836(74)90048-5. [DOI] [PubMed] [Google Scholar]
  9. Goldman R. D., Rebhun L. I. The structure and some properties of the isolated mitotic apparatus. J Cell Sci. 1969 Jan;4(1):179–209. doi: 10.1242/jcs.4.1.179. [DOI] [PubMed] [Google Scholar]
  10. Good N. E., Winget G. D., Winter W., Connolly T. N., Izawa S., Singh R. M. Hydrogen ion buffers for biological research. Biochemistry. 1966 Feb;5(2):467–477. doi: 10.1021/bi00866a011. [DOI] [PubMed] [Google Scholar]
  11. Harris P. The role of membranes in the ogranization of the mitotic apparatus. Exp Cell Res. 1975 Sep;94(2):409–425. doi: 10.1016/0014-4827(75)90507-8. [DOI] [PubMed] [Google Scholar]
  12. Hartmann J. F., Zimmerman A. M. The isolated mitotic apparatus. Studies on nucleoproteins. Exp Cell Res. 1968 May;50(2):403–417. doi: 10.1016/0014-4827(68)90459-x. [DOI] [PubMed] [Google Scholar]
  13. Head J. F., Mader S., Kaminer B. Calcium-binding modulator protein from the unfertilized egg of the sea urchin Arbacia punctulata. J Cell Biol. 1979 Jan;80(1):211–218. doi: 10.1083/jcb.80.1.211. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Helenius A., Simons K. Solubilization of membranes by detergents. Biochim Biophys Acta. 1975 Mar 25;415(1):29–79. doi: 10.1016/0304-4157(75)90016-7. [DOI] [PubMed] [Google Scholar]
  15. Inoué S., Fuseler J., Salmon E. D., Ellis G. W. Functional organization of mitotic microtubules. Physical chemistry of the in vivo equilibrium system. Biophys J. 1975 Jul;15(7):725–744. doi: 10.1016/S0006-3495(75)85850-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Inoué S., Sato H. Cell motility by labile association of molecules. The nature of mitotic spindle fibers and their role in chromosome movement. J Gen Physiol. 1967 Jul;50(6 Suppl):259–292. [PMC free article] [PubMed] [Google Scholar]
  17. KANE R. E. The mitotic apparatus: isolation by controlled pH. J Cell Biol. 1962 Jan;12:47–55. doi: 10.1083/jcb.12.1.47. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Kirschner M. W. Microtubule assembly and nucleation. Int Rev Cytol. 1978;54:1–71. doi: 10.1016/s0074-7696(08)60164-3. [DOI] [PubMed] [Google Scholar]
  19. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  20. Marcum J. M., Dedman J. R., Brinkley B. R., Means A. R. Control of microtubule assembly-disassembly by calcium-dependent regulator protein. Proc Natl Acad Sci U S A. 1978 Aug;75(8):3771–3775. doi: 10.1073/pnas.75.8.3771. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Mazia D., Petzelt C., Williams R. O., Meza I. A Ca-activated ATPase in the mitotic apparatus of the sea urchin egg (isolated by a new method). Exp Cell Res. 1972 Feb;70(2):325–332. doi: 10.1016/0014-4827(72)90143-7. [DOI] [PubMed] [Google Scholar]
  22. Nishida E., Kumagai H. Calcium sensitivity of sea urchin tubulin in in vitro assembly and the effects of calcium-dependent regulator (CDR) proteins isolated from sea urchin eggs and porcine brains. J Biochem. 1980 Jan;87(1):143–151. doi: 10.1093/oxfordjournals.jbchem.a132719. [DOI] [PubMed] [Google Scholar]
  23. Olmsted J. B., Borisy G. G. Ionic and nucleotide requirements for microtubule polymerization in vitro. Biochemistry. 1975 Jul;14(13):2996–3005. doi: 10.1021/bi00684a032. [DOI] [PubMed] [Google Scholar]
  24. PORTZEHL H., CALDWELL P. C., RUEEGG J. C. THE DEPENDENCE OF CONTRACTION AND RELAXATION OF MUSCLE FIBRES FROM THE CRAB MAIA SQUINADO ON THE INTERNAL CONCENTRATION OF FREE CALCIUM IONS. Biochim Biophys Acta. 1964 May 25;79:581–591. doi: 10.1016/0926-6577(64)90224-4. [DOI] [PubMed] [Google Scholar]
  25. Petzelt C., von Ledebur-Villiger M. Ca2+-stimulated ATPase during the early development of parthenogenetically activated eggs of the sea urchin Paracentrotus lividus. Exp Cell Res. 1973 Sep;81(1):87–94. doi: 10.1016/0014-4827(73)90114-6. [DOI] [PubMed] [Google Scholar]
  26. Rasmussen H., Goodman D. B. Calcium and cAMP as interrelated intracellular messengers. Ann N Y Acad Sci. 1975 Jun 30;253:789–796. doi: 10.1111/j.1749-6632.1975.tb19247.x. [DOI] [PubMed] [Google Scholar]
  27. Rebhun L. I. Cyclic nucleotides, calcium, and cell division. Int Rev Cytol. 1977;49:1–54. doi: 10.1016/s0074-7696(08)61946-4. [DOI] [PubMed] [Google Scholar]
  28. Rebhun L. I., Mellon M., Jemiolo D., Nath J., Ivy N. Regulation of size and birefringence of the in vivo mitotic apparatus. J Supramol Struct. 1974;2(2-4):466–485. doi: 10.1002/jss.400020232. [DOI] [PubMed] [Google Scholar]
  29. Rebhun L. I., Rosenbaum J., Lefebvre P., Smith G. Reversible restoration of the birefringence of cold-treated, isolated mitotic apparatus of surf clam eggs with chick brain tubulin. Nature. 1974 May 10;249(453):113–115. doi: 10.1038/249113a0. [DOI] [PubMed] [Google Scholar]
  30. Robbins E., Jentzsch G. Ultrastructural changes in the mitotic apparatus at the metaphase-to-anaphase transition. J Cell Biol. 1969 Mar;40(3):678–691. doi: 10.1083/jcb.40.3.678. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Rose B., Loewenstein W. R. Calcium ion distribution in cytoplasm visualised by aequorin: diffusion in cytosol restricted by energized sequestering. Science. 1975 Dec 19;190(4220):1204–1206. doi: 10.1126/science.1198106. [DOI] [PubMed] [Google Scholar]
  32. Sakai H., Shimoda S., Hiramoto Y. Mass isolation of mitotic apparatus using a glycerol/Mg2+/Triton X-100 medium. Exp Cell Res. 1977 Feb;104(2):457–461. doi: 10.1016/0014-4827(77)90117-3. [DOI] [PubMed] [Google Scholar]
  33. Salmon E. D., Ellis G. W. Compensator transducer increases ease, accuracy, and rapidity of measuring changes in specimen birefringence with polarization microscopy. J Microsc. 1976 Jan;106(1):63–69. doi: 10.1111/j.1365-2818.1976.tb02384.x. [DOI] [PubMed] [Google Scholar]
  34. Salmon E. D. Pressure-induced depolymerization of brain microtubules in vitro. Science. 1975 Sep 12;189(4206):884–886. doi: 10.1126/science.1171523. [DOI] [PubMed] [Google Scholar]
  35. Salmon E. D. Pressure-induced depolymerization of spindle microtubules. I. Changes in birefringence and spindle length. J Cell Biol. 1975 Jun;65(3):603–614. doi: 10.1083/jcb.65.3.603. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Salmon E. D. Spindle microtubules: thermodynamics of in vivo assembly and role in chromosome movement. Ann N Y Acad Sci. 1975 Jun 30;253:383–406. doi: 10.1111/j.1749-6632.1975.tb19216.x. [DOI] [PubMed] [Google Scholar]
  37. Sato H., Ellis G. W., Inoué S. Microtubular origin of mitotic spindle form birefringence. Demonstration of the applicability of Wiener's equation. J Cell Biol. 1975 Dec;67(3):501–517. doi: 10.1083/jcb.67.3.501. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Schliwa M. The role of divalent cations in the regulation of microtubule assembly. In vivo studies on microtubules of the heliozoan axopodium using the ionophore A23187. J Cell Biol. 1976 Sep;70(3):527–540. doi: 10.1083/jcb.70.3.527. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Steinhardt R., Zucker R., Schatten G. Intracellular calcium release at fertilization in the sea urchin egg. Dev Biol. 1977 Jul 1;58(1):185–196. doi: 10.1016/0012-1606(77)90084-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Weber A., Herz R. The relationship between caffeine contracture of intact muscle and the effect of caffeine on reticulum. J Gen Physiol. 1968 Nov;52(5):750–759. doi: 10.1085/jgp.52.5.750. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Weber A. The mechanism of the action of caffeine on sarcoplasmic reticulum. J Gen Physiol. 1968 Nov;52(5):760–772. doi: 10.1085/jgp.52.5.760. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. 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]
  43. Welsh M. J., Dedman J. R., Brinkley B. R., Means A. R. Calcium-dependent regulator protein: localization in mitotic apparatus of eukaryotic cells. Proc Natl Acad Sci U S A. 1978 Apr;75(4):1867–1871. doi: 10.1073/pnas.75.4.1867. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. 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]
  45. Yount R. G., Babcock D., Ballantyne W., Ojala D. Adenylyl imidodiphosphate, an adenosine triphosphate analog containing a P--N--P linkage. Biochemistry. 1971 Jun 22;10(13):2484–2489. doi: 10.1021/bi00789a009. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES