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. 1990 Jun 1;110(6):1965–1973. doi: 10.1083/jcb.110.6.1965

The actin released from profilin--actin complexes is insufficient to account for the increase in F-actin in chemoattractant-stimulated polymorphonuclear leukocytes

PMCID: PMC2116129  PMID: 2351690

Abstract

Chemoattractant stimulation of polymorphonuclear leukocytes is associated with a nearly two-fold rise in actin filament content. We examined the role of the actin monomer sequestering protein, profilin, in the regulation of PMN actin filament assembly during chemoattractant stimulation using a Triton extraction method. Poly-L-proline-conjugated Sepharose beads were used to assess the relative concentration of actin bound to profilin with high enough affinity to withstand dilution (profilin-actin complex) and DNase I-conjugated beads to measure the relative concentration of actin in the Triton-soluble fraction not bound to profilin. Actin associated with the Triton-insoluble fraction (F-actin) was also measured. In unstimulated PMN, the relative concentration of actin bound to profilin was maximum. After FMLP stimulation, profilin released actin monomers within 10 s, with the profilin-actin complex concentration reaching a nadir by 40 s and remaining low as long as the cells were exposed to chemoattractant (up to 30 min). If FMLP was dissociated from PMN membrane receptors using t- BOC, actin reassociated with profilin within 20 s. Quantitative analysis of these reactions, however, revealed that profilin release of and rebinding to actin could account for only a small percentage of the total change in F-actin content. Determination of the total profilin and actin concentrations in PMN revealed that the molar ratio of profilin to actin was 1 to 5.2. When purified actin was polymerized in PMN Triton extract containing EGTA, removal of profilin from the extract minimally affected (12% reduction) the high apparent critical concentration at which actin began to assemble. Although profilin released actin at the appropriate time to stimulate actin assembly during exposure to chemoattractants, the concentration of profilin in PMN was insufficient to explain the high unpolymerized actin content in unstimulated PMN and the quantity of actin released from profilin too small to account for the large shifts from unpolymerized to polymerized actin associated with maximal chemoattractant stimulation.

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Selected References

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  1. Amrein P. C., Stossel T. P. Prevention of degradation of human polymorphonuclear leukocyte proteins by diisopropylfluorophosphate. Blood. 1980 Sep;56(3):442–447. [PubMed] [Google Scholar]
  2. Bamburg J. R., Bray D. Distribution and cellular localization of actin depolymerizing factor. J Cell Biol. 1987 Dec;105(6 Pt 1):2817–2825. doi: 10.1083/jcb.105.6.2817. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bamburg J. R., Harris H. E., Weeds A. G. Partial purification and characterization of an actin depolymerizing factor from brain. FEBS Lett. 1980 Nov 17;121(1):178–182. doi: 10.1016/0014-5793(80)81292-0. [DOI] [PubMed] [Google Scholar]
  4. Blikstad I., Sundkvist I., Eriksson S. Isolation and characterization of profilactin and profilin from calf thymus and brain. Eur J Biochem. 1980 Apr;105(3):425–433. doi: 10.1111/j.1432-1033.1980.tb04517.x. [DOI] [PubMed] [Google Scholar]
  5. Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1006/abio.1976.9999. [DOI] [PubMed] [Google Scholar]
  6. Carlsson L., Nyström L. E., Sundkvist I., Markey F., Lindberg U. Actin polymerizability is influenced by profilin, a low molecular weight protein in non-muscle cells. J Mol Biol. 1977 Sep 25;115(3):465–483. doi: 10.1016/0022-2836(77)90166-8. [DOI] [PubMed] [Google Scholar]
  7. 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]
  8. Chaponnier C., Yin H. L., Stossel T. P. Reversibility of gelsolin/actin interaction in macrophages. Evidence of Ca2+-dependent and Ca2+-independent pathways. J Exp Med. 1987 Jan 1;165(1):97–106. doi: 10.1084/jem.165.1.97. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. DiNubile M. J., Southwick F. S. Effects of macrophage profilin on actin in the presence and absence of acumentin and gelsolin. J Biol Chem. 1985 Jun 25;260(12):7402–7409. [PubMed] [Google Scholar]
  10. 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]
  11. Forehand J. R., Pabst M. J., Phillips W. A., Johnston R. B., Jr Lipopolysaccharide priming of human neutrophils for an enhanced respiratory burst. Role of intracellular free calcium. J Clin Invest. 1989 Jan;83(1):74–83. doi: 10.1172/JCI113887. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Guthrie L. A., McPhail L. C., Henson P. M., Johnston R. B., Jr Priming of neutrophils for enhanced release of oxygen metabolites by bacterial lipopolysaccharide. Evidence for increased activity of the superoxide-producing enzyme. J Exp Med. 1984 Dec 1;160(6):1656–1671. doi: 10.1084/jem.160.6.1656. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Harris H. E., Weeds A. G. Platelet actin: sub-cellular distribution and association with profilin. FEBS Lett. 1978 Jun 1;90(1):84–88. doi: 10.1016/0014-5793(78)80303-2. [DOI] [PubMed] [Google Scholar]
  14. Hartwig J. H., Chambers K. A., Hopcia K. L., Kwiatkowski D. J. Association of profilin with filament-free regions of human leukocyte and platelet membranes and reversible membrane binding during platelet activation. J Cell Biol. 1989 Oct;109(4 Pt 1):1571–1579. doi: 10.1083/jcb.109.4.1571. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. 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]
  16. 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]
  17. Kwiatkowski D. J., Bruns G. A. Human profilin. Molecular cloning, sequence comparison, and chromosomal analysis. J Biol Chem. 1988 Apr 25;263(12):5910–5915. [PubMed] [Google Scholar]
  18. Lal A. A., Korn E. D. Reinvestigation of the inhibition of actin polymerization by profilin. J Biol Chem. 1985 Aug 25;260(18):10132–10138. [PubMed] [Google Scholar]
  19. Lambooy P. K., Korn E. D. Purification and characterization of actobindin, a new actin monomer-binding protein from Acanthamoeba castellanii. J Biol Chem. 1986 Dec 25;261(36):17150–17155. [PubMed] [Google Scholar]
  20. Larsson H., Lindberg U. The effect of divalent cations on the interaction between calf spleen profilin and different actins. Biochim Biophys Acta. 1988 Mar 2;953(1):95–105. doi: 10.1016/0167-4838(88)90013-1. [DOI] [PubMed] [Google Scholar]
  21. Lassing I., Lindberg U. Evidence that the phosphatidylinositol cycle is linked to cell motility. Exp Cell Res. 1988 Jan;174(1):1–15. doi: 10.1016/0014-4827(88)90136-x. [DOI] [PubMed] [Google Scholar]
  22. Lassing I., Lindberg U. Specific interaction between phosphatidylinositol 4,5-bisphosphate and profilactin. Nature. 1985 Apr 4;314(6010):472–474. doi: 10.1038/314472a0. [DOI] [PubMed] [Google Scholar]
  23. 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]
  24. Maekawa S., Nishida E., Ohta Y., Sakai H. Isolation of low molecular weight actin-binding proteins from porcine brain. J Biochem. 1984 Feb;95(2):377–385. doi: 10.1093/oxfordjournals.jbchem.a134618. [DOI] [PubMed] [Google Scholar]
  25. Markey F., Lindberg U., Eriksson L. Human platelets contain profilin, a potential regulator of actin polymerisability. FEBS Lett. 1978 Apr 1;88(1):75–79. doi: 10.1016/0014-5793(78)80610-3. [DOI] [PubMed] [Google Scholar]
  26. Markey F., Persson T., Lindberg U. Characterization of platelet extracts before and after stimulation with respect to the possible role of profilactin as microfilament precursor. Cell. 1981 Jan;23(1):145–153. doi: 10.1016/0092-8674(81)90279-8. [DOI] [PubMed] [Google Scholar]
  27. Mc Leod J. F., Kowalski M. A., Haddad J. G., Jr Interactions among serum vitamin D binding protein, monomeric actin, profilin, and profilactin. J Biol Chem. 1989 Jan 15;264(2):1260–1267. [PubMed] [Google Scholar]
  28. Nishida E., Maekawa S., Sakai H. Cofilin, a protein in porcine brain that binds to actin filaments and inhibits their interactions with myosin and tropomyosin. Biochemistry. 1984 Oct 23;23(22):5307–5313. doi: 10.1021/bi00317a032. [DOI] [PubMed] [Google Scholar]
  29. Northrop J., Weber A., Mooseker M. S., Franzini-Armstrong C., Bishop M. F., Dubyak G. R., Tucker M., Walsh T. P. Different calcium dependence of the capping and cutting activities of villin. J Biol Chem. 1986 Jul 15;261(20):9274–9281. [PubMed] [Google Scholar]
  30. O'Farrell P. H. High resolution two-dimensional electrophoresis of proteins. J Biol Chem. 1975 May 25;250(10):4007–4021. [PMC free article] [PubMed] [Google Scholar]
  31. Ozaki K., Sugino H., Hasegawa T., Takahashi S., Hatano S. Isolation and characterization of Physarum profilin. J Biochem. 1983 Jan;93(1):295–298. doi: 10.1093/oxfordjournals.jbchem.a134167. [DOI] [PubMed] [Google Scholar]
  32. Reichstein E., Korn E. D. Acanthamoeba profilin. A protein of low molecular weight from Acanpthamoeba castellanii that inhibits actin nucleation. J Biol Chem. 1979 Jul 10;254(13):6174–6179. [PubMed] [Google Scholar]
  33. Shalit M., Dabiri G. A., Southwick F. S. Platelet-activating factor both stimulates and "primes" human polymorphonuclear leukocyte actin filament assembly. Blood. 1987 Dec;70(6):1921–1927. [PubMed] [Google Scholar]
  34. 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]
  35. Sonobe S., Takahashi S., Hatano S., Kuroda K. Phosphorylation of Amoeba G-actin and its effect on actin polymerization. J Biol Chem. 1986 Nov 5;261(31):14837–14843. [PubMed] [Google Scholar]
  36. 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]
  37. Southwick F. S., Stossel T. P. Isolation of an inhibitor of actin polymerization from human polymorphonuclear leukocytes. J Biol Chem. 1981 Mar 25;256(6):3030–3036. [PubMed] [Google Scholar]
  38. Spudich J. A., Watt S. The regulation of rabbit skeletal muscle contraction. I. Biochemical studies of the interaction of the tropomyosin-troponin complex with actin and the proteolytic fragments of myosin. J Biol Chem. 1971 Aug 10;246(15):4866–4871. [PubMed] [Google Scholar]
  39. Tanaka M., Shibata H. Poly(L-proline)-binding proteins from chick embryos are a profilin and a profilactin. Eur J Biochem. 1985 Sep 2;151(2):291–297. doi: 10.1111/j.1432-1033.1985.tb09099.x. [DOI] [PubMed] [Google Scholar]
  40. Tseng P. C., Pollard T. D. Mechanism of action of Acanthamoeba profilin: demonstration of actin species specificity and regulation by micromolar concentrations of MgCl2. J Cell Biol. 1982 Jul;94(1):213–218. doi: 10.1083/jcb.94.1.213. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Tseng P. C., Runge M. S., Cooper J. A., Williams R. C., Jr, Pollard T. D. Physical, immunochemical, and functional properties of Acanthamoeba profilin. J Cell Biol. 1984 Jan;98(1):214–221. doi: 10.1083/jcb.98.1.214. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. 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]
  43. White J. R., Naccache P. H., Sha'afi R. I. Stimulation by chemotactic factor of actin association with the cytoskeleton in rabbit neutrophils. Effects of calcium and cytochalasin B. J Biol Chem. 1983 Nov 25;258(22):14041–14047. [PubMed] [Google Scholar]
  44. Zechel K. Isolation of polymerization-competent cytoplasmic actin by affinity chromatography on immobilized DNAse I using formamide as eluant. Eur J Biochem. 1980 Sep;110(2):343–348. doi: 10.1111/j.1432-1033.1980.tb04873.x. [DOI] [PubMed] [Google Scholar]

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