Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1989 Jul 1;109(1):211–223. doi: 10.1083/jcb.109.1.211

Cell cycle-dependent changes in the dynamics of MAP 2 and MAP 4 in cultured cells

PMCID: PMC2115460  PMID: 2745548

Abstract

To examine the behavior of microtubule-associated proteins (MAPs) in living cells, MAP 4 and MAP 2 have been derivatized with 6- iodoacetamido-fluorescein, and the distribution of microinjected MAP has been analyzed using a low light level video system and fluorescence redistribution after photobleaching. Within 1 min following microinjection of fluoresceinated MAP 4 or MAP 2, fluorescent microtubule arrays were visible in interphase or mitotic PtK1 cells. After cold treatment of fluorescent MAP 2-containing cells (3 h, 4 degrees C), microtubule fluorescence disappeared, and the only fluorescence above background was located at the centrosomes; microtubule patterns returned upon warming. Loss of microtubule immunofluorescence after nocodozole treatment was similar in MAP- injected and control cells, suggesting that injected fluorescein- labeled MAP 2 did not stabilize microtubules. The dynamics of the MAPs were examined further by FRAP. FRAP analysis of interphase cells demonstrated that MAP 2 redistributed with half-times slightly longer (60 +/- 25 s) than those for MAP 4 (44 +/- 20 s), but both types of MAPs bound to microtubules in vivo exchanged with soluble MAPs at rates exceeding the rate of tubulin turnover. These data imply that microtubules in interphase cells are assembled with constantly exchanging populations of MAP. Metaphase cells at 37 degrees C or 26 degrees C showed similar mean redistribution half-times for both MAP 2 and MAP 4; these were 3-4 fold faster than the interphase rates (MAP 2, t1/2 = 14 +/- 6 s; MAP 4, t1/2 = 17 +/- 5 s). The extent of recovery of spindle fluorescence in MAP-injected cells was to 84-94% at either 26 or 37 degrees C. Although most metaphase tubulin, like the MAPs, turns over rapidly and completely under physiologic conditions, published work shows either reduced rates or extents of turnover at 26 degrees C, suggesting that the fast mitotic MAP exchange is not simply because of fast tubulin turnover. Exchange of MAP 4 bound to telophase midbodies occurred with dynamics comparable to those seen in metaphase spindles (t1/2 = approximately 27 s) whereas midbody tubulin exchange was slow (greater than 300 s). These data demonstrate that the rate of MAP exchange on microtubules is a function of time in the cell cycle.

Full Text

The Full Text of this article is available as a PDF (5.1 MB).

Selected References

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

  1. Bernhardt R., Matus A. Light and electron microscopic studies of the distribution of microtubule-associated protein 2 in rat brain: a difference between dendritic and axonal cytoskeletons. J Comp Neurol. 1984 Jun 20;226(2):203–221. doi: 10.1002/cne.902260205. [DOI] [PubMed] [Google Scholar]
  2. Binder L. I., Frankfurter A., Rebhun L. I. The distribution of tau in the mammalian central nervous system. J Cell Biol. 1985 Oct;101(4):1371–1378. doi: 10.1083/jcb.101.4.1371. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Black M. M., Greene L. A. Changes in the colchicine susceptibility of microtubules associated with neurite outgrowth: studies with nerve growth factor-responsive PC12 pheochromocytoma cells. J Cell Biol. 1982 Nov;95(2 Pt 1):379–386. doi: 10.1083/jcb.95.2.379. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bloom G. S., Schoenfeld T. A., Vallee R. B. Widespread distribution of the major polypeptide component of MAP 1 (microtubule-associated protein 1) in the nervous system. J Cell Biol. 1984 Jan;98(1):320–330. doi: 10.1083/jcb.98.1.320. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Borisy G. G., Marcum J. M., Olmsted J. B., Murphy D. B., Johnson K. A. Purification of tubulin and associated high molecular weight proteins from porcine brain and characterization of microtubule assembly in vitro. Ann N Y Acad Sci. 1975 Jun 30;253:107–132. doi: 10.1111/j.1749-6632.1975.tb19196.x. [DOI] [PubMed] [Google Scholar]
  6. Bulinski J. C., Borisy G. G. Self-assembly of microtubules in extracts of cultured HeLa cells and the identification of HeLa microtubule-associated proteins. Proc Natl Acad Sci U S A. 1979 Jan;76(1):293–297. doi: 10.1073/pnas.76.1.293. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Bulinski J. C., Borisy G. G. Widespread distribution of a 210,000 mol wt microtubule-associated protein in cells and tissues of primates. J Cell Biol. 1980 Dec;87(3 Pt 1):802–808. doi: 10.1083/jcb.87.3.802. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Caceres A., Payne M. R., Binder L. I., Steward O. Immunocytochemical localization of actin and microtubule-associated protein MAP2 in dendritic spines. Proc Natl Acad Sci U S A. 1983 Mar;80(6):1738–1742. doi: 10.1073/pnas.80.6.1738. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Carlier M. F., Simon C., Pantaloni D. Polymorphism of tubulin oligomers in the presence of microtubule-associated proteins. Implications in microtubule assembly. Biochemistry. 1984 Mar 27;23(7):1582–1590. doi: 10.1021/bi00302a037. [DOI] [PubMed] [Google Scholar]
  10. Cassimeris L. U., Wadsworth P., Salmon E. D. Dynamics of microtubule depolymerization in monocytes. J Cell Biol. 1986 Jun;102(6):2023–2032. doi: 10.1083/jcb.102.6.2023. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Cassimeris L., Pryer N. K., Salmon E. D. Real-time observations of microtubule dynamic instability in living cells. J Cell Biol. 1988 Dec;107(6 Pt 1):2223–2231. doi: 10.1083/jcb.107.6.2223. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Cleveland D. W., Hwo S. Y., Kirschner M. W. Purification of tau, a microtubule-associated protein that induces assembly of microtubules from purified tubulin. J Mol Biol. 1977 Oct 25;116(2):207–225. doi: 10.1016/0022-2836(77)90213-3. [DOI] [PubMed] [Google Scholar]
  13. Connolly J. A., Kalnins V. I. Tau and HMW microtubule-associated proteins have different microtubule binding sites in vivo. Eur J Cell Biol. 1980 Aug;21(3):296–300. [PubMed] [Google Scholar]
  14. Drubin D. G., Feinstein S. C., Shooter E. M., Kirschner M. W. Nerve growth factor-induced neurite outgrowth in PC12 cells involves the coordinate induction of microtubule assembly and assembly-promoting factors. J Cell Biol. 1985 Nov;101(5 Pt 1):1799–1807. doi: 10.1083/jcb.101.5.1799. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Drubin D. G., Kirschner M. W. Tau protein function in living cells. J Cell Biol. 1986 Dec;103(6 Pt 2):2739–2746. doi: 10.1083/jcb.103.6.2739. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Drubin D., Kobayashi S., Kirschner M. Association of tau protein with microtubules in living cells. Ann N Y Acad Sci. 1986;466:257–268. doi: 10.1111/j.1749-6632.1986.tb38398.x. [DOI] [PubMed] [Google Scholar]
  17. Díez J. C., de la Torre J., Avila J. Differential association of the different brain microtubule proteins in different in vitro assembly conditions. Biochim Biophys Acta. 1985 Jan 28;838(1):32–38. [PubMed] [Google Scholar]
  18. Goldstein L. S., Laymon R. A., McIntosh J. R. A microtubule-associated protein in Drosophila melanogaster: identification, characterization, and isolation of coding sequences. J Cell Biol. 1986 Jun;102(6):2076–2087. doi: 10.1083/jcb.102.6.2076. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Greene L. A., Liem R. K., Shelanski M. L. Regulation of a high molecular weight microtubule-associated protein in PC12 cells by nerve growth factor. J Cell Biol. 1983 Jan;96(1):76–83. doi: 10.1083/jcb.96.1.76. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Hiller G., Weber K. Radioimmunoassay for tubulin: a quantitative comparison of the tubulin content of different established tissue culture cells and tissues. Cell. 1978 Aug;14(4):795–804. doi: 10.1016/0092-8674(78)90335-5. [DOI] [PubMed] [Google Scholar]
  21. Izant J. G., Weatherbee J. A., McIntosh J. R. A microtubule-associated protein antigen unique to mitotic spindle microtubules in PtK1 cells. J Cell Biol. 1983 Feb;96(2):424–434. doi: 10.1083/jcb.96.2.424. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Keith C. H., Feramisco J. R., Shelanski M. Direct visualization of fluorescein-labeled microtubules in vitro and in microinjected fibroblasts. J Cell Biol. 1981 Jan;88(1):234–240. doi: 10.1083/jcb.88.1.234. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Leslie R. J., Saxton W. M., Mitchison T. J., Neighbors B., Salmon E. D., McIntosh J. R. Assembly properties of fluorescein-labeled tubulin in vitro before and after fluorescence bleaching. J Cell Biol. 1984 Dec;99(6):2146–2156. doi: 10.1083/jcb.99.6.2146. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Lewis S. A., Wang D. H., Cowan N. J. Microtubule-associated protein MAP2 shares a microtubule binding motif with tau protein. Science. 1988 Nov 11;242(4880):936–939. doi: 10.1126/science.3142041. [DOI] [PubMed] [Google Scholar]
  25. Magendantz M., Solomon F. Analyzing the components of microtubules: antibodies against chartins, associated proteins from cultured cells. Proc Natl Acad Sci U S A. 1985 Oct;82(19):6581–6585. doi: 10.1073/pnas.82.19.6581. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Mitchison T., Evans L., Schulze E., Kirschner M. Sites of microtubule assembly and disassembly in the mitotic spindle. Cell. 1986 May 23;45(4):515–527. doi: 10.1016/0092-8674(86)90283-7. [DOI] [PubMed] [Google Scholar]
  27. Morrissey J. H. Silver stain for proteins in polyacrylamide gels: a modified procedure with enhanced uniform sensitivity. Anal Biochem. 1981 Nov 1;117(2):307–310. doi: 10.1016/0003-2697(81)90783-1. [DOI] [PubMed] [Google Scholar]
  28. Olmsted J. B., Asnes C. F., Parysek L. M., Lyon H. D., Kidder G. M. Distribution of MAP-4 in cells and in adult and developing mouse tissues. Ann N Y Acad Sci. 1986;466:292–305. doi: 10.1111/j.1749-6632.1986.tb38401.x. [DOI] [PubMed] [Google Scholar]
  29. Olmsted J. B., Cox J. V., Asnes C. F., Parysek L. M., Lyon H. D. Cellular regulation of microtubule organization. J Cell Biol. 1984 Jul;99(1 Pt 2):28s–32s. doi: 10.1083/jcb.99.1.28s. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Olmsted J. B., Lyon H. D. A microtubule-associated protein specific to differentiated neuroblastoma cells. J Biol Chem. 1981 Apr 10;256(7):3507–3511. [PubMed] [Google Scholar]
  31. Parysek L. M., Asnes C. F., Olmsted J. B. MAP 4: occurrence in mouse tissues. J Cell Biol. 1984 Oct;99(4 Pt 1):1309–1315. doi: 10.1083/jcb.99.4.1309. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Parysek L. M., Wolosewick J. J., Olmsted J. B. MAP 4: a microtubule-associated protein specific for a subset of tissue microtubules. J Cell Biol. 1984 Dec;99(6):2287–2296. doi: 10.1083/jcb.99.6.2287. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Parysek L. M., del Cerro M., Olmsted J. B. Microtubule-associated protein 4 antibody: a new marker for astroglia and oligodendroglia. Neuroscience. 1985 Jul;15(3):869–875. doi: 10.1016/0306-4522(85)90084-3. [DOI] [PubMed] [Google Scholar]
  34. 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]
  35. Salmon E. D., Leslie R. J., Saxton W. M., Karow M. L., McIntosh J. R. Spindle microtubule dynamics in sea urchin embryos: analysis using a fluorescein-labeled tubulin and measurements of fluorescence redistribution after laser photobleaching. J Cell Biol. 1984 Dec;99(6):2165–2174. doi: 10.1083/jcb.99.6.2165. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Saxton W. M., McIntosh J. R. Interzone microtubule behavior in late anaphase and telophase spindles. J Cell Biol. 1987 Aug;105(2):875–886. doi: 10.1083/jcb.105.2.875. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Saxton W. M., Stemple D. L., Leslie R. J., Salmon E. D., Zavortink M., McIntosh J. R. Tubulin dynamics in cultured mammalian cells. J Cell Biol. 1984 Dec;99(6):2175–2186. doi: 10.1083/jcb.99.6.2175. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Scherson T., Kreis T. E., Schlessinger J., Littauer U. Z., Borisy G. G., Geiger B. Dynamic interactions of fluorescently labeled microtubule-associated proteins in living cells. J Cell Biol. 1984 Aug;99(2):425–434. doi: 10.1083/jcb.99.2.425. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Schulze E., Kirschner M. Microtubule dynamics in interphase cells. J Cell Biol. 1986 Mar;102(3):1020–1031. doi: 10.1083/jcb.102.3.1020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Sheetz M. P., Koppel D. E. Membrane damage caused by irradiation of fluorescent concanavalin A. Proc Natl Acad Sci U S A. 1979 Jul;76(7):3314–3317. doi: 10.1073/pnas.76.7.3314. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Shelanski M. L., Gaskin F., Cantor C. R. Microtubule assembly in the absence of added nucleotides. Proc Natl Acad Sci U S A. 1973 Mar;70(3):765–768. doi: 10.1073/pnas.70.3.765. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Soltys B. J., Borisy G. G. Polymerization of tubulin in vivo: direct evidence for assembly onto microtubule ends and from centrosomes. J Cell Biol. 1985 May;100(5):1682–1689. doi: 10.1083/jcb.100.5.1682. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Stemple D. L., Sweet S. C., Welsh M. J., McIntosh J. R. Dynamics of a fluorescent calmodulin analog in the mammalian mitotic spindle at metaphase. Cell Motil Cytoskeleton. 1988;9(3):231–242. doi: 10.1002/cm.970090305. [DOI] [PubMed] [Google Scholar]
  44. Vallee R. B. A taxol-dependent procedure for the isolation of microtubules and microtubule-associated proteins (MAPs). J Cell Biol. 1982 Feb;92(2):435–442. doi: 10.1083/jcb.92.2.435. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Vandenbunder B., Borisy G. G. Decoration of microtubules by fluorescently labeled microtubule-associated protein 2 (MAP2) does not interfere with their spatial organization and progress through mitosis in living fibroblasts. Cell Motil Cytoskeleton. 1986;6(6):570–579. doi: 10.1002/cm.970060605. [DOI] [PubMed] [Google Scholar]
  46. Vigers G. P., Coue M., McIntosh J. R. Fluorescent microtubules break up under illumination. J Cell Biol. 1988 Sep;107(3):1011–1024. doi: 10.1083/jcb.107.3.1011. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Wadsworth P., Salmon E. D. Analysis of the treadmilling model during metaphase of mitosis using fluorescence redistribution after photobleaching. J Cell Biol. 1986 Mar;102(3):1032–1038. doi: 10.1083/jcb.102.3.1032. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Wadsworth P., Salmon E. D. Microtubule dynamics in mitotic spindles of living cells. Ann N Y Acad Sci. 1986;466:580–592. doi: 10.1111/j.1749-6632.1986.tb38434.x. [DOI] [PubMed] [Google Scholar]
  49. Walker R. A., O'Brien E. T., Pryer N. K., Soboeiro M. F., Voter W. A., Erickson H. P., Salmon E. D. Dynamic instability of individual microtubules analyzed by video light microscopy: rate constants and transition frequencies. J Cell Biol. 1988 Oct;107(4):1437–1448. doi: 10.1083/jcb.107.4.1437. [DOI] [PMC free article] [PubMed] [Google Scholar]

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

RESOURCES