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. 1989 Nov 1;109(5):2207–2213. doi: 10.1083/jcb.109.5.2207

Identification of actin nucleation activity and polymerization inhibitor in ameboid cells: their regulation by chemotactic stimulation

PMCID: PMC2115889  PMID: 2553744

Abstract

Actin polymerization occurs in amebae of Dictyostelium discoideum after chemotactic stimulation (Hall, A. L., A. Schlein, and J. Condeelis. 1988. J. Cell. Biochem. 37:285-299). When cells are lysed with Triton X- 100 during stimulation, an actin nucleation activity is detected in lysates by measuring the rate of pyrene-labeled actin polymerization. This stimulated nucleation activity is closely correlated with actin polymerization observed in vivo in its kinetics, developmental regulation, and cytochalasin D sensitivity. Actin polymerization is coordinate with pseudopod extension in synchronized populations of cells and is correlated with the accumulation of F actin in pseudopods. The stimulated actin nucleation activity is present in low-speed pellets from Triton lysates (cytoskeletons) within 3 s of stimulation and is stable compared with the nucleation activity of whole cell lysates. Low-speed supernatants contain a reversible inhibitor of the actin nucleation activity that is itself regulated by chemotactic stimulation. Neither activity requires Ca2+ and both are fully expressed in 10 mM EGTA. Fractions containing the inhibitor do not sever actin filaments but do inhibit actin polymerization that is seeded by fragments of purified F actin. These results indicate that chemotactic stimulation of Dictyostelium discoideum generates both an actin-nucleating activity and an actin-polymerization inhibitor, and suggest that the parallel regulation of these two activities leads to the transient phases of actin polymerization observed in vivo. The different compartmentation of these two activities may account for polarized pseudopod extension in gradients of chemoattractant.

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Selected References

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  1. André E., Lottspeich F., Schleicher M., Noegel A. Severin, gelsolin, and villin share a homologous sequence in regions presumed to contain F-actin severing domains. J Biol Chem. 1988 Jan 15;263(2):722–727. [PubMed] [Google Scholar]
  2. Bonder E. M., Mooseker M. S. Cytochalasin B slows but does not prevent monomer addition at the barbed end of the actin filament. J Cell Biol. 1986 Jan;102(1):282–288. doi: 10.1083/jcb.102.1.282. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bonner J. T., Hall E. M., Sachsenmaier W., Walker B. K. Evidence for a second chemotactic system in the cellular slime mold, Dictyostelium discoideum. J Bacteriol. 1970 Jun;102(3):682–687. doi: 10.1128/jb.102.3.682-687.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Brenner M., Thoms S. D. Caffeine blocks activation of cyclic AMP synthesis in Dictyostelium discoideum. Dev Biol. 1984 Jan;101(1):136–146. doi: 10.1016/0012-1606(84)90124-6. [DOI] [PubMed] [Google Scholar]
  5. Bumann J., Wurster B., Malchow D. Attractant-induced changes and oscillations of the extracellular Ca++ concentration in suspensions of differentiating Dictyostelium cells. J Cell Biol. 1984 Jan;98(1):173–178. doi: 10.1083/jcb.98.1.173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Carson M., Weber A., Zigmond S. H. An actin-nucleating activity in polymorphonuclear leukocytes is modulated by chemotactic peptides. J Cell Biol. 1986 Dec;103(6 Pt 2):2707–2714. doi: 10.1083/jcb.103.6.2707. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Condeelis J. S., Taylor D. L. The contractile basis of amoeboid movement. V. The control of gelation, solation, and contraction in extracts from Dictyostelium discoideum. J Cell Biol. 1977 Sep;74(3):901–927. doi: 10.1083/jcb.74.3.901. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Condeelis J., Hall A., Bresnick A., Warren V., Hock R., Bennett H., Ogihara S. Actin polymerization and pseudopod extension during amoeboid chemotaxis. Cell Motil Cytoskeleton. 1988;10(1-2):77–90. doi: 10.1002/cm.970100113. [DOI] [PubMed] [Google Scholar]
  9. Cooper J. A., Walker S. B., Pollard T. D. Pyrene actin: documentation of the validity of a sensitive assay for actin polymerization. J Muscle Res Cell Motil. 1983 Apr;4(2):253–262. doi: 10.1007/BF00712034. [DOI] [PubMed] [Google Scholar]
  10. Detmers P. A., Goodenough U. W., Condeelis J. Elongation of the fertilization tubule in Chlamydomonas: new observations on the core microfilaments and the effect of transient intracellular signals on their structural integrity. J Cell Biol. 1983 Aug;97(2):522–532. doi: 10.1083/jcb.97.2.522. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Dharmawardhane S., Warren V., Hall A. L., Condeelis J. Changes in the association of actin-binding proteins with the actin cytoskeleton during chemotactic stimulation of Dictyostelium discoideum. Cell Motil Cytoskeleton. 1989;13(1):57–63. doi: 10.1002/cm.970130107. [DOI] [PubMed] [Google Scholar]
  12. Europe-Finner G. N., Newell P. C. Inositol 1,4,5-trisphosphate and calcium stimulate actin polymerization in Dictyostelium discoideum. J Cell Sci. 1986 Jun;82:41–51. doi: 10.1242/jcs.82.1.41. [DOI] [PubMed] [Google Scholar]
  13. Futrelle R. P., Traut J., McKee W. G. Cell behavior in Dictyostelium discoideum: preaggregation response to localized cyclic AMP pulses. J Cell Biol. 1982 Mar;92(3):807–821. doi: 10.1083/jcb.92.3.807. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Galvin N. J., Stockhausen D., Meyers-Hutchins B. L., Frazier W. A. Association of the cyclic AMP chemotaxis receptor with the detergent-insoluble cytoskeleton of Dictyostelium discoideum. J Cell Biol. 1984 Feb;98(2):584–595. doi: 10.1083/jcb.98.2.584. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Giffard R. G., Spudich J. A., Spudich A. Ca2+-sensitive isolation of a cortical actin matrix from Dictyostelium amoebae. J Muscle Res Cell Motil. 1983 Feb;4(1):115–131. doi: 10.1007/BF00711962. [DOI] [PubMed] [Google Scholar]
  16. Gomer R. H., Armstrong D., Leichtling B. H., Firtel R. A. cAMP induction of prespore and prestalk gene expression in Dictyostelium is mediated by the cell-surface cAMP receptor. Proc Natl Acad Sci U S A. 1986 Nov;83(22):8624–8628. doi: 10.1073/pnas.83.22.8624. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Hall A. L., Schlein A., Condeelis J. Relationship of pseudopod extension to chemotactic hormone-induced actin polymerization in amoeboid cells. J Cell Biochem. 1988 Jul;37(3):285–299. doi: 10.1002/jcb.240370304. [DOI] [PubMed] [Google Scholar]
  18. Lind S. E., Janmey P. A., Chaponnier C., Herbert T. J., Stossel T. P. Reversible binding of actin to gelsolin and profilin in human platelet extracts. J Cell Biol. 1987 Aug;105(2):833–842. doi: 10.1083/jcb.105.2.833. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. McRobbie S. J., Newell P. C. Changes in actin associated with the cytoskeleton following chemotactic stimulation of dictyostelium discoideum. Biochem Biophys Res Commun. 1983 Aug 30;115(1):351–359. doi: 10.1016/0006-291x(83)91011-2. [DOI] [PubMed] [Google Scholar]
  20. Pollard T. D., Cooper J. A. Actin and actin-binding proteins. A critical evaluation of mechanisms and functions. Annu Rev Biochem. 1986;55:987–1035. doi: 10.1146/annurev.bi.55.070186.005011. [DOI] [PubMed] [Google Scholar]
  21. Schaap P., van Driel R. V. Induction of post-aggregative differentiation in Dictyostelium discoideum by cAMP. Evidence of involvement of the cell surface cAMP receptor. Exp Cell Res. 1985 Aug;159(2):388–398. doi: 10.1016/s0014-4827(85)80012-4. [DOI] [PubMed] [Google Scholar]
  22. Schleicher M., Gerisch G., Isenberg G. New actin-binding proteins from Dictyostelium discoideum. EMBO J. 1984 Sep;3(9):2095–2100. doi: 10.1002/j.1460-2075.1984.tb02096.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Selve N., Wegner A. Rate constants and equilibrium constants for binding of the gelsolin-actin complex to the barbed ends of actin filaments in the presence and absence of calcium. Eur J Biochem. 1986 Oct 15;160(2):379–387. doi: 10.1111/j.1432-1033.1986.tb09982.x. [DOI] [PubMed] [Google Scholar]
  24. Swanson J. A., Taylor D. L. Local and spatially coordinated movements in Dictyostelium discoideum amoebae during chemotaxis. Cell. 1982 Feb;28(2):225–232. doi: 10.1016/0092-8674(82)90340-3. [DOI] [PubMed] [Google Scholar]
  25. Theibert A., Palmisano M., Jastorff B., Devreotes P. The specificity of the cAMP receptor mediating activation of adenylate cyclase in Dictyostelium discoideum. Dev Biol. 1986 Apr;114(2):529–533. doi: 10.1016/0012-1606(86)90216-2. [DOI] [PubMed] [Google Scholar]
  26. Varnum-Finney B. J., Voss E., Soll D. R. Frequency and orientation of pseudopod formation of Dictyostelium discoideum amebae chemotaxing in a spatial gradient: further evidence for a temporal mechanism. Cell Motil Cytoskeleton. 1987;8(1):18–26. doi: 10.1002/cm.970080104. [DOI] [PubMed] [Google Scholar]
  27. Wanger M., Wegner A. Equilibrium constant for binding of an actin filament capping protein to the barbed end of actin filaments. Biochemistry. 1985 Feb 12;24(4):1035–1040. doi: 10.1021/bi00325a035. [DOI] [PubMed] [Google Scholar]
  28. Yamamoto K., Pardee J. D., Reidler J., Stryer L., Spudich J. A. Mechanism of interaction of Dictyostelium severin with actin filaments. J Cell Biol. 1982 Dec;95(3):711–719. doi: 10.1083/jcb.95.3.711. [DOI] [PMC free article] [PubMed] [Google Scholar]

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