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. 1992 May 2;117(4):765–774. doi: 10.1083/jcb.117.4.765

Relationship of F-actin distribution to development of polar shape in human polymorphonuclear neutrophils

PMCID: PMC2289466  PMID: 1577856

Abstract

Polymerization of actin has been associated with development of polar shape in human neutrophils (PMN). To examine the relation of filamentous actin (F-actin) distribution to shape change in PMN, we developed a method using computerized video image analysis and fluorescence microscopy to quantify distribution of F-actin in single cells. PMN were labeled with fluorescent probe NBD-phallicidin to measure filamentous actin and Texas red to assess cell thickness. We show that Texas red fluorescence is a reasonable measure of cell thickness and that correction of the NBD-phallicidin image for cell thickness using the Texas red image permits assessment of focal F-actin content. Parameters were derived that quantify total F-actin content, movement of F-actin away from the center of the cell, asymmetry of F- actin distribution, and change from round to polar shape. The sequence of change in F-actin distribution and its relation to development of polar shape in PMN was determined using these parameters. After stimulation with chemotactic peptide at 25 degrees C, F-actin polymerized first at the rim of the PMN. This was followed by development of asymmetry of F-actin distribution and change to polar shape. The dominant pseudopod developed first in the region of lower F- actin concentration followed later by polymerization of actin in the end of the developed pseudopod. Asymmetric F-actin distribution was detected in round PMN before development of polar shape. Based upon these data, asymmetric distribution of F-actin is coincident with and probably precedes development of polar shape in PMN stimulated in suspension by chemotactic peptide.

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Selected References

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  1. Blikstad I., Carlsson L. On the dynamics of the microfilament system in HeLa cells. J Cell Biol. 1982 Apr;93(1):122–128. doi: 10.1083/jcb.93.1.122. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Brennan P. J., Zigmond S. H., Schreiber A. D., Smith E. R., Southwick F. S. Binding of IgG containing immune complexes to human neutrophil Fc gamma RII and Fc gamma RIII induces actin polymerization by a pertussis toxin-insensitive transduction pathway. J Immunol. 1991 Jun 15;146(12):4282–4288. [PubMed] [Google Scholar]
  3. Cassimeris L., McNeill H., Zigmond S. H. Chemoattractant-stimulated polymorphonuclear leukocytes contain two populations of actin filaments that differ in their spatial distributions and relative stabilities. J Cell Biol. 1990 Apr;110(4):1067–1075. doi: 10.1083/jcb.110.4.1067. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Condeelis J., Bresnick A., Demma M., Dharmawardhane S., Eddy R., Hall A. L., Sauterer R., Warren V. Mechanisms of amoeboid chemotaxis: an evaluation of the cortical expansion model. Dev Genet. 1990;11(5-6):333–340. doi: 10.1002/dvg.1020110504. [DOI] [PubMed] [Google Scholar]
  5. Diaz G., Quacci D., Dell'Orbo C. Recognition of cell surface modulation by elliptic Fourier analysis. Comput Methods Programs Biomed. 1990 Jan;31(1):57–62. doi: 10.1016/0169-2607(90)90031-4. [DOI] [PubMed] [Google Scholar]
  6. Fechheimer M., Zigmond S. H. Changes in cytoskeletal proteins of polymorphonuclear leukocytes induced by chemotactic peptides. Cell Motil. 1983;3(4):349–361. doi: 10.1002/cm.970030406. [DOI] [PubMed] [Google Scholar]
  7. Greenberg S., el Khoury J., di Virgilio F., Kaplan E. M., Silverstein S. C. Ca(2+)-independent F-actin assembly and disassembly during Fc receptor-mediated phagocytosis in mouse macrophages. J Cell Biol. 1991 May;113(4):757–767. doi: 10.1083/jcb.113.4.757. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Grinstein S., Furuya W., Cragoe E. J., Jr Volume changes in activated human neutrophils: the role of Na+/H+ exchange. J Cell Physiol. 1986 Jul;128(1):33–40. doi: 10.1002/jcp.1041280107. [DOI] [PubMed] [Google Scholar]
  9. 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]
  10. Harvath L. Regulation of neutrophil chemotaxis: correlations with actin polymerization. Cancer Invest. 1990;8(6):651–654. doi: 10.3109/07357909009018937. [DOI] [PubMed] [Google Scholar]
  11. Hiraoka Y., Sedat J. W., Agard D. A. Determination of three-dimensional imaging properties of a light microscope system. Partial confocal behavior in epifluorescence microscopy. Biophys J. 1990 Feb;57(2):325–333. doi: 10.1016/S0006-3495(90)82534-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Howard T. H., Oresajo C. O. A method for quantifying F-actin in chemotactic peptide activated neutrophils: study of the effect of tBOC peptide. Cell Motil. 1985;5(6):545–557. doi: 10.1002/cm.970050609. [DOI] [PubMed] [Google Scholar]
  13. Howard T. H., Oresajo C. O. The kinetics of chemotactic peptide-induced change in F-actin content, F-actin distribution, and the shape of neutrophils. J Cell Biol. 1985 Sep;101(3):1078–1085. doi: 10.1083/jcb.101.3.1078. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Howard T. H., Wang D., Berkow R. L. Lipopolysaccharide modulates chemotactic peptide-induced actin polymerization in neutrophils. J Leukoc Biol. 1990 Jan;47(1):13–24. doi: 10.1002/jlb.47.1.13. [DOI] [PubMed] [Google Scholar]
  15. Howard T., Chaponnier C., Yin H., Stossel T. Gelsolin-actin interaction and actin polymerization in human neutrophils. J Cell Biol. 1990 Jun;110(6):1983–1991. doi: 10.1083/jcb.110.6.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. MacFarlane G. D., Herzberg M. C., Nelson R. D. Analysis of polarization and orientation of human polymorphonuclear leukocytes by computer-interfaced video microscopy. J Leukoc Biol. 1987 Apr;41(4):307–317. doi: 10.1002/jlb.41.4.307. [DOI] [PubMed] [Google Scholar]
  17. Nathan C., Sanchez E. Tumor necrosis factor and CD11/CD18 (beta 2) integrins act synergistically to lower cAMP in human neutrophils. J Cell Biol. 1990 Nov;111(5 Pt 1):2171–2181. doi: 10.1083/jcb.111.5.2171. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Oliver J. M., Krawiec J. A., Becker E. L. The distribution of actin during chemotaxis in rabbit neutrophils. J Reticuloendothel Soc. 1978 Dec;24(6):697–704. [PubMed] [Google Scholar]
  19. Oster G. F., Perelson A. S. The physics of cell motility. J Cell Sci Suppl. 1987;8:35–54. doi: 10.1242/jcs.1987.supplement_8.3. [DOI] [PubMed] [Google Scholar]
  20. Scanlon M., Williams D. A., Fay F. S. A Ca2+-insensitive form of fura-2 associated with polymorphonuclear leukocytes. Assessment and accurate Ca2+ measurement. J Biol Chem. 1987 May 5;262(13):6308–6312. [PubMed] [Google Scholar]
  21. Senda N., Tamura H., Shibata N., Yoshitake J., Konko K., Tanaka K. The mechanism of the movement of leucocytes. Exp Cell Res. 1975 Mar 15;91(2):393–407. doi: 10.1016/0014-4827(75)90120-2. [DOI] [PubMed] [Google Scholar]
  22. Sklar L. A., Omann G. M., Painter R. G. Relationship of actin polymerization and depolymerization to light scattering in human neutrophils: dependence on receptor occupancy and intracellular Ca++. J Cell Biol. 1985 Sep;101(3):1161–1166. doi: 10.1083/jcb.101.3.1161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Southwick F. S., Dabiri G. A., Paschetto M., Zigmond S. H. Polymorphonuclear leukocyte adherence induces actin polymerization by a transduction pathway which differs from that used by chemoattractants. J Cell Biol. 1989 Oct;109(4 Pt 1):1561–1569. doi: 10.1083/jcb.109.4.1561. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Stossel T. P. From signal to pseudopod. How cells control cytoplasmic actin assembly. J Biol Chem. 1989 Nov 5;264(31):18261–18264. [PubMed] [Google Scholar]
  25. Symons M. H., Mitchison T. J. Control of actin polymerization in live and permeabilized fibroblasts. J Cell Biol. 1991 Aug;114(3):503–513. doi: 10.1083/jcb.114.3.503. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Wallace P. J., Wersto R. P., Packman C. H., Lichtman M. A. Chemotactic peptide-induced changes in neutrophil actin conformation. J Cell Biol. 1984 Sep;99(3):1060–1065. doi: 10.1083/jcb.99.3.1060. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Wang Y. L. Mobility of filamentous actin in living cytoplasm. J Cell Biol. 1987 Dec;105(6 Pt 1):2811–2816. doi: 10.1083/jcb.105.6.2811. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Watson P. A. Function follows form: generation of intracellular signals by cell deformation. FASEB J. 1991 Apr;5(7):2013–2019. doi: 10.1096/fasebj.5.7.1707019. [DOI] [PubMed] [Google Scholar]
  29. Watts R. G., Crispens M. A., Howard T. H. A quantitative study of the role of F-actin in producing neutrophil shape. Cell Motil Cytoskeleton. 1991;19(3):159–168. doi: 10.1002/cm.970190304. [DOI] [PubMed] [Google Scholar]
  30. Watts R. G., Howard T. H. Evidence for a gelsolin-rich, labile F-actin pool in human polymorphonuclear leukocytes. Cell Motil Cytoskeleton. 1992;21(1):25–37. doi: 10.1002/cm.970210104. [DOI] [PubMed] [Google Scholar]
  31. Wymann M. P., Kernen P., Bengtsson T., Andersson T., Baggiolini M., Deranleau D. A. Corresponding oscillations in neutrophil shape and filamentous actin content. J Biol Chem. 1990 Jan 15;265(2):619–622. [PubMed] [Google Scholar]
  32. Zigmond S. H., Levitsky H. I., Kreel B. J. Cell polarity: an examination of its behavioral expression and its consequences for polymorphonuclear leukocyte chemotaxis. J Cell Biol. 1981 Jun;89(3):585–592. doi: 10.1083/jcb.89.3.585. [DOI] [PMC free article] [PubMed] [Google Scholar]

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