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. 1977 Feb 1;72(2):339–350. doi: 10.1083/jcb.72.2.339

Structural and biochemical aspects of cell motility in amebas of Dictyostelium discoideum

PMCID: PMC2111002  PMID: 188829

Abstract

Amebas of Dictyostelium discoideum contain both microfilaments and microtubules. Microfilaments, found primarily in a cortical filament network, aggregate into bundles when glycerinated cells contract in response to Mg-ATP. These cortical filaments bind heavy meromyosin. Microtubules are sparse in amebas before aggregation. Colchicine, griseofulvin, or cold treatments do not affect cell motility or cell shape. Saltatory movement of cytoplasmic particles is inhibited by these treatments and the particles subsequently accumulate in the posterior of the cell. Cell motility rate changes as Dicytostelium amebas go through different stages of the life cycle. Quantitation of cellular actin by sodium dodecyl sulfate-polyacrylamide gel electrophoresis shows that the quantity of cellular actin changes during the life cycle. These changes in actin are directly correlated with changes in motility rate. Addition of cyclic AMP to Dictyostelium cultures at the end of the feeding stage prevents a decline in motility rate during the preaggregation stage. Cyclic AMP also modifies the change in actin content of the cells during preaggregation.

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Selected References

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  1. Adelstein R. S., Conti M. A., Johnson G. S., Pastan I., Pollard T. D. Isolation and characterization of myosin from cloned mouse fibroblasts. Proc Natl Acad Sci U S A. 1972 Dec;69(12):3693–3697. doi: 10.1073/pnas.69.12.3693. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Allen R. D., Taylor D. L. The molecular basis of amoeboid movement. Soc Gen Physiol Ser. 1975;30:239–258. [PubMed] [Google Scholar]
  3. Bonner J. T. Aggregation and differentiation in the cellular slime molds. Annu Rev Microbiol. 1971;25:75–92. doi: 10.1146/annurev.mi.25.100171.000451. [DOI] [PubMed] [Google Scholar]
  4. 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]
  5. Bray D., Brownlee S. M. Peptide mapping of proteins from acrylamide gels. Anal Biochem. 1973 Sep;55(1):213–221. doi: 10.1016/0003-2697(73)90306-0. [DOI] [PubMed] [Google Scholar]
  6. Clarke M., Schatten G., Mazia D., Spudich J. A. Visualization of actin fibers associated with the cell membrane in amoebae of Dictyostelium discoideum. Proc Natl Acad Sci U S A. 1975 May;72(5):1758–1762. doi: 10.1073/pnas.72.5.1758. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Clarke M., Spudich J. A. Biochemical and structural studies of actomyosin-like proteins from non-muscle cells. Isolation and characterization of myosin from amoebae of Dictyostelium discoideum. J Mol Biol. 1974 Jun 25;86(2):209–222. doi: 10.1016/0022-2836(74)90013-8. [DOI] [PubMed] [Google Scholar]
  8. Francis D. Cyclic AMP-induced changes in protein synthesis in a cellular slime mould, Polysphondylium pallidum. Nature. 1975 Dec 25;258(5537):763–765. doi: 10.1038/258763a0. [DOI] [PubMed] [Google Scholar]
  9. Gail M. H., Boone C. W. Effect of colcemid on fibroblast motility. Exp Cell Res. 1971 Mar;65(1):221–227. doi: 10.1016/s0014-4827(71)80070-8. [DOI] [PubMed] [Google Scholar]
  10. Gail M. H., Boone C. W. The locomotion of mouse fibroblasts in tissue culture. Biophys J. 1970 Oct;10(10):980–993. doi: 10.1016/S0006-3495(70)86347-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Garrod D. R., Born G. V. Effect of temperature on the mutual adhesion of preaggregation cells of the slime mould, Dictyostelium discoideum. J Cell Sci. 1971 May;8(3):751–765. doi: 10.1242/jcs.8.3.751. [DOI] [PubMed] [Google Scholar]
  12. Kane R. E. Preparation and purification of polymerized actin from sea urchin egg extracts. J Cell Biol. 1975 Aug;66(2):305–315. doi: 10.1083/jcb.66.2.305. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. 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]
  14. Malchow D., Gerisch G. Short-term binding and hydrolysis of cyclic 3':5'-adenosine monophosphate by aggregating Dictyostelium cells. Proc Natl Acad Sci U S A. 1974 Jun;71(6):2423–2427. doi: 10.1073/pnas.71.6.2423. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Pannbacker R. G., Bravard L. J. Phosphodiesterase in Dictyostelium discoideum and the chemotactic response to cyclic adenosine monophosphate. Science. 1972 Mar 3;175(4025):1014–1015. doi: 10.1126/science.175.4025.1014. [DOI] [PubMed] [Google Scholar]
  16. Pollard T. D. Functional implications of the biochemical and structural properties of cytoplasmic contractile proteins. Soc Gen Physiol Ser. 1975;30:259–286. [PubMed] [Google Scholar]
  17. Pollard T. D. The role of actin in the temperature-dependent gelation and contraction of extracts of Acanthamoeba. J Cell Biol. 1976 Mar;68(3):579–601. doi: 10.1083/jcb.68.3.579. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Pollard T. D., Weihing R. R. Actin and myosin and cell movement. CRC Crit Rev Biochem. 1974 Jan;2(1):1–65. doi: 10.3109/10409237409105443. [DOI] [PubMed] [Google Scholar]
  19. SAMUEL E. W. Orientation and rate of locomotion of individual amebas in the life cycle of the cellular slime mold Dictyostelium mucoroides. Dev Biol. 1961 Jun;3:317–335. doi: 10.1016/0012-1606(61)90050-1. [DOI] [PubMed] [Google Scholar]
  20. SIMARD-DUQUESNE N., COUILLARD P. Ameboid movement, I. Reactivation of glycerinated models of Amoeba proteus with adenosinetriphosphate. Exp Cell Res. 1962 Oct;28:85–91. doi: 10.1016/0014-4827(62)90314-2. [DOI] [PubMed] [Google Scholar]
  21. SZENT-GYORGYI A. G. Meromyosins, the subunits of myosin. Arch Biochem Biophys. 1953 Feb;42(2):305–320. doi: 10.1016/0003-9861(53)90360-9. [DOI] [PubMed] [Google Scholar]
  22. Spudich J. A. Biochemical and structural studies of actomyosin-like proteins from non-muscle cells. II. Purification, properties, and membrane association of actin from amoebae of Dictyostelium discoideum. J Biol Chem. 1974 Sep 25;249(18):6013–6020. [PubMed] [Google Scholar]
  23. Spudich J. A., Clarke M. The contractile proteins of Dictyostelium discoideum. J Supramol Struct. 1974;2(2-4):150–162. doi: 10.1002/jss.400020209. [DOI] [PubMed] [Google Scholar]
  24. Spurr A. R. A low-viscosity epoxy resin embedding medium for electron microscopy. J Ultrastruct Res. 1969 Jan;26(1):31–43. doi: 10.1016/s0022-5320(69)90033-1. [DOI] [PubMed] [Google Scholar]
  25. Taylor D. L., Rhodes J. A., Hammond S. A. The contractile basis of ameboid movement. II. Structure and contractility of motile extracts and plasmalemma-ectoplasm ghosts. J Cell Biol. 1976 Jul;70(1):123–143. doi: 10.1083/jcb.70.1.123. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Tuchman J., Alton T., Lodish H. F. Preferential synthesis of actin during early development of the slime mold Dictyostelium discoideum. Dev Biol. 1974 Sep;40(1):116–128. doi: 10.1016/0012-1606(74)90113-4. [DOI] [PubMed] [Google Scholar]
  27. Woolley D. E. An actin-like protein from amoebae of dictyostelium discoideum. Arch Biochem Biophys. 1972 Jun;150(2):519–530. doi: 10.1016/0003-9861(72)90070-7. [DOI] [PubMed] [Google Scholar]

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