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. 1984 Sep 1;99(3):894–899. doi: 10.1083/jcb.99.3.894

Localization of actin and myosin for the study of ameboid movement in Dictyostelium using improved immunofluorescence

PMCID: PMC2113401  PMID: 6381508

Abstract

The distribution of actin and myosin in Dictyostelium amebae at different developmental stages was studied by improved immunofluorescence ("agar-overlay" technique). Both were localized at the cortical region of amebae in all early developmental stages. In amebae with polarized morphology, bright fluorescence with antiactin was seen in the anterior pseudopode. The cortex in the posterior end was also stained with antiactin. On the other hand, very specific crescent-shaped staining with antimyosin was seen at the posterior cortex. In cells in contact with each other, actin was concentrated at the contact region, whereas myosin was localized specifically in the cortex on the other side of the contact region. At the aggregation stage, when monopodial amebae migrate forming streams, actin staining was seen all around the cell periphery, with intense fluorescence in the anterior pseudopode. On the other hand, specific staining of myosin was seen only at the posterior cortex. The cleavage furrow of cells performing cytokinesis displayed distinct myosin staining, and this staining represented the filamentous structure aligned in parallel to the axis of constriction. These findings indicate that myosin staining reflects the portion of the cell cortex where contraction occurs and the motive force of ameboid movement is generated at the posterior cortex of a migrating cell.

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Selected References

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  1. Amato P. A., Unanue E. R., Taylor D. L. Distribution of actin in spreading macrophages: a comparative study on living and fixed cells. J Cell Biol. 1983 Mar;96(3):750–761. doi: 10.1083/jcb.96.3.750. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Brier J., Fechheimer M., Swanson J., Taylor D. L. Abundance, relative gelation activity, and distribution of the 95,000-dalton actin-binding protein from Dictyostelium discoideum. J Cell Biol. 1983 Jul;97(1):178–185. doi: 10.1083/jcb.97.1.178. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. 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]
  4. Condeelis J., Vahey M. A calcium- and pH-regulated protein from Dictyostelium discoideum that cross-links actin filaments. J Cell Biol. 1982 Aug;94(2):466–471. doi: 10.1083/jcb.94.2.466. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Dulbecco R., Allen R., Okada S., Bowman M. Functional changes of intermediate filaments in fibroblastic cells revealed by a monoclonal antibody. Proc Natl Acad Sci U S A. 1983 Apr;80(7):1915–1918. doi: 10.1073/pnas.80.7.1915. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Eckert B. S., Lazarides E. Localization of actin in Dictyostelium amebas by immunofluorescence. J Cell Biol. 1978 Jun;77(3):714–721. doi: 10.1083/jcb.77.3.714. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Engvall E., Perlmann P. Enzyme-linked immunosorbent assay, Elisa. 3. Quantitation of specific antibodies by enzyme-labeled anti-immunoglobulin in antigen-coated tubes. J Immunol. 1972 Jul;109(1):129–135. [PubMed] [Google Scholar]
  8. Fukui Y. Intranuclear actin bundles induced by dimethyl sulfoxide in interphase nucleus of Dictyostelium. J Cell Biol. 1978 Jan;76(1):146–157. doi: 10.1083/jcb.76.1.146. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Fukui Y., Katsumaru H. Dynamics of nuclear actin bundle induction by dimethyl sulfoxide and factors affecting its development. J Cell Biol. 1980 Jan;84(1):131–140. doi: 10.1083/jcb.84.1.131. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. 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]
  11. Hellewell S. B., Taylor D. L. The contractile basis of ameboid movement. VI. The solation-contraction coupling hypothesis. J Cell Biol. 1979 Dec;83(3):633–648. doi: 10.1083/jcb.83.3.633. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Huxley H. E. The mechanism of muscular contraction. Science. 1969 Jun 20;164(3886):1356–1365. doi: 10.1126/science.164.3886.1356. [DOI] [PubMed] [Google Scholar]
  13. Johnson G. D., Nogueira Araujo G. M. A simple method of reducing the fading of immunofluorescence during microscopy. J Immunol Methods. 1981;43(3):349–350. doi: 10.1016/0022-1759(81)90183-6. [DOI] [PubMed] [Google Scholar]
  14. Kuczmarski E. R., Spudich J. A. Regulation of myosin self-assembly: phosphorylation of Dictyostelium heavy chain inhibits formation of thick filaments. Proc Natl Acad Sci U S A. 1980 Dec;77(12):7292–7296. doi: 10.1073/pnas.77.12.7292. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kuriyama R., Sato C., Fukui Y., Nishibayashi S. In vitro nucleation of microtubules from microtubule-organizing center prepared from cellular slime mold. Cell Motil. 1982;2(3):257–272. doi: 10.1002/cm.970020306. [DOI] [PubMed] [Google Scholar]
  16. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  17. Mockrin S. C., Spudich J. A. Calcium control of actin-activated myosin adenosine triphosphatase from Dictyostelium discoideum. Proc Natl Acad Sci U S A. 1976 Jul;73(7):2321–2325. doi: 10.1073/pnas.73.7.2321. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Naib-Majani W., Stockem W., Wohlfarth-Bottermann K. E., Osborn M., Weber K. Immunocytochemistry of the acellular slime mold Physarum polycephalum. II. Spatial organization of cytoplasmic actin. Eur J Cell Biol. 1982 Aug;28(1):103–114. [PubMed] [Google Scholar]
  19. RODRIGUEZ J., DEINHARDT F. Preparation of a semipermanent mounting medium for fluorescent antibody studies. Virology. 1960 Oct;12:316–317. doi: 10.1016/0042-6822(60)90205-1. [DOI] [PubMed] [Google Scholar]
  20. Roos U. P. Mitosis in the cellular slime mold Polysphondylium violaceum. J Cell Biol. 1975 Feb;64(2):480–491. doi: 10.1083/jcb.64.2.480. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Rubino S., Fighetti M., Unger E., Cappuccinelli P. Location of actin, myosin, and microtubular structures during directed locomotion of Dictyostelium amebae. J Cell Biol. 1984 Feb;98(2):382–390. doi: 10.1083/jcb.98.2.382. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Salisbury J. L., Condeelis J. S., Maihle N. J., Satir P. Calmodulin localization during capping and receptor-mediated endocytosis. Nature. 1981 Nov 12;294(5837):163–166. doi: 10.1038/294163a0. [DOI] [PubMed] [Google Scholar]
  23. Shulman M., Wilde C. D., Köhler G. A better cell line for making hybridomas secreting specific antibodies. Nature. 1978 Nov 16;276(5685):269–270. doi: 10.1038/276269a0. [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. Towbin H., Staehelin T., Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci U S A. 1979 Sep;76(9):4350–4354. doi: 10.1073/pnas.76.9.4350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Watts D. J., Ashworth J. M. Growth of myxameobae of the cellular slime mould Dictyostelium discoideum in axenic culture. Biochem J. 1970 Sep;119(2):171–174. doi: 10.1042/bj1190171. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Yumura S., Fukui Y. Filopodelike projections induced with dimethyl sulfoxide and their relevance to cellular polarity in Dictyostelium. J Cell Biol. 1983 Mar;96(3):857–865. doi: 10.1083/jcb.96.3.857. [DOI] [PMC free article] [PubMed] [Google Scholar]

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