Tyrosine phosphorylation: a signal for the activation of the phagocyte respiratory burst

References

• Roos D. The involvement of oxygen radicals in microbicidal mechanisms of leukocytes and macrophages. Klin Wochenschr 1991; 69: 975–980.
   PubMedGoogle Scholar
• Morel F, Doussiere J, Vignais P V. The superoxide-generating oxidase of phagocytic cells. Physiological, molecular and pathological aspects. Eur J Biochem 1991; 201: 523–546.
   PubMedGoogle Scholar
• Halliwell B. Oxidants and human disease: some new concepts. FASEB J 1987; 1: 358–364.
   PubMed Web of Science ®Google Scholar
• Thelen M, Dewald B, Baggiolini M. Neutrophil signal transduction and activation of the respiratory burst. Physiol Rev 1993; 73: 797–821.
   PubMed Web of Science ®Google Scholar
• Tauber A I. Protein kinase C and the activation of the human neutrophil NADPH-oxidase. Blood 1987; 69: 711–720.
   PubMed Web of Science ®Google Scholar
• Eckhart W, Hutchinson M A, Hunter T. An activity phosphorylating tyrosine in polyoma T antigen immunoprecipitates. Cell 1979; 18: 925–933.
   PubMed Web of Science ®Google Scholar
• Hunter T, Cooper J A. Protein-tyrosine kinases. Ann Rev Biochem 1985; 54: 897–930.
   PubMed Web of Science ®Google Scholar
• Hunter T. A thousand and one protein kinases. Cell 1987; 50: 823–829.
   PubMed Web of Science ®Google Scholar
• Wang J Y J. Antibodies for phosphotyrosine: analytical and preparative tool for tyrosyl-phosphorylated proteins. Anal Biochem 1988; 172: 1–7.
   PubMed Web of Science ®Google Scholar
• Cantley L C, Auger K R, Carpenter C et al. Oncogenes and signal transduction. Cell 1991; 64: 281–302.
   PubMed Web of Science ®Google Scholar
• Pawson T. Tyrosine kinases and their interactions with signalling proteins. Curr Opin Genet Dev 1992; 2: 4–12.
   PubMed Web of Science ®Google Scholar
• Kraft A S, Berkow R L. Tyrosine kinase and phosphotyrosine phosphatase activity in human promyelocytic leukemia cells and human polymorphonuclear leukocytes. Blood 1987; 70: 356–362.
   PubMed Web of Science ®Google Scholar
• Berkow R L, Dodson R W, Kraft A S. Human neutrophils contain distinct cytosolic and particulate tyrosine kinase activities: possible role in neutrophil activation. Biochim Biophys Acta 1989; 997: 292–301.
   PubMed Web of Science ®Google Scholar
• Nasmith P E, Mills G B, Grinstein S. Guanine nucleotides induce tyrosine phosphorylation and activation of the respiratory burst in neutrophils. Biochem J 1989; 257: 893–897.
   PubMed Web of Science ®Google Scholar
• Gomez-Cambronero J, Huang C K, Bonak V A et al. Tyrosine phosphorylation in human neutrophil. Biochem Biophys Res Commun 1989; 162: 1478–1485.
   PubMed Web of Science ®Google Scholar
• Huang C-K, Laramee G R, Casnellie J E. Chemotactic factor induced tyrosine phosphorylation of membrane associated proteins in rabbit peritoneal neutrophils. Biochem Biophys Res Commun 1988; 151: 794–801.
   PubMed Web of Science ®Google Scholar
• Kusunoki T, Higashi H, Hosoi S et al. Tyrosine phosphorylation and its possible role in superoxide production by human neutrophils stimulated with FMLP and IgG. Biochem Biophys Res Commun 1992; 183: 789–796.
   PubMed Web of Science ®Google Scholar
• Torres M, Hall F L, O'Neill K. Stimulation of human neutrophils with formyl-methionyl-leucyl-phenylalanine induces tyrosine phosphorylation and activation of two distinct mitogen-activated protein-kinases. J Immunol 1993; 150: 1563–1577.
   PubMed Web of Science ®Google Scholar
• Huang C K, Laramee G R, Casnellie J E. Chemotactic factor induced tyrosine phosphorylation of membrane associated proteins in rabbit peritoneal neutrophils. Biochem Biophys Res Commun 1988; 151: 794–801.
   PubMed Web of Science ®Google Scholar
• Richard S, Farrell C A, Shaw A S, Showell H J, Connelly P A. C5a as a model for chemotactic factor-stimulated tyrosine phosphorylation in the human neutrophil. J Immunol 1994; 152: 2479–2487.
   PubMed Web of Science ®Google Scholar
• Ohta S, Inazu T, Taniguchi T, Nakagawara G, Yamamura H. Protein-tyrosine phosphorylations induced by concanavalin A and N-formyl-methionyl-leucyl-phenylalanine in human neutrophils. Eur J Biochem 1992; 206: 895–900.
   PubMedGoogle Scholar
• Gaudry M, Roberge C J, de Medicis R, Lussier A, Poubelle P E, Naccache P H. Crystal-induced neutrophil activation. III. Inflammatory microcrystals induce a distinct pattern of tyrosine phosphorylation in human neutrsophils. J Clin Invest 1994; 91: 1649–1655.
   Web of Science ®Google Scholar
• Green S P, Hamilton J A, Phillips W A. Zymosan-triggered tyrosine phosphorylation in mouse bone-marrow-derived macrophages is enhanced by respiratory-burst priming agents. Biochem J 1992; 288: 427–432.
   PubMed Web of Science ®Google Scholar
• Boulet I, Ralph S, Stanley E et al. LPS- and IFN-γ-induced expression of hck and lyn tyrosine kinases in murine bone marrow-derived macrophages. Oncogene 1992; 7: 703–710.
   PubMed Web of Science ®Google Scholar
• Green S P, Phillips W A. Activation of the macrophage respiratory burst by phorbol myristate acetate: evidence for both tyrosine kinase dependent and independent pathways. Biochim Biophys Acta 1994; 1222: 241–248.
   PubMed Web of Science ®Google Scholar
• Dryden P, Duronio V, Martin L, Hudson A T, Salari H. Inhibition of human neutrophil responses by α-cyano-3,4-dihydroxythiocinnamamide; a protein-tyrosine kinase inhibitor. Br J Pharmacol 1992; 106: 656–664.
   PubMed Web of Science ®Google Scholar
• Rollet E, Caon A C, Roberge C J et al. Tyrosine phosphorylation in activated human neutrophils. Comparison of the effects of different classes of agonists and identification of the signaling pathways involved. J Immunol 1994; 153: 353–363.
   PubMed Web of Science ®Google Scholar
• Gomez-Cambronero J, Yamazaki M, Metwally F et al. Granulocyte-macrophage colony-stimulating factor and human neutrophils: role of guanine nucleotide regulatory proteins. Proc Natl Acad Sci USA 1989; 86: 3569–3573.
   Google Scholar
• Grinstein S, Furuya W. Tyrosine phosphorylation and oxygen consumption induced by G proteins in neutrophils. Am J Physiol Cell Physiol 1991; 260: C1019–C1027.
   Web of Science ®Google Scholar
• Fialkow L, Chan C K, Grinstein S, Downey G P. Regulation of tyrosine phosphorylation in neutrophils by the NADPH oxidase-role of reactive oxygen intermediates. J Biol Chem 1993; 268: 17131–17137.
   PubMed Web of Science ®Google Scholar
• Naccache P H, Gilbert C, Caon A C et al. Selective inhibition of human neutrophil functional responsiveness by erbstatin, an inhibitor of tyrosine protein kinase. Blood 1990; 76: 2098–2104.
   PubMed Web of Science ®Google Scholar
• Azuma E K, Kitagawa S, Yuo A et al. Activation of the respiratory burst and tyrosine phosphorylation of proteins in human neutrophils—no direct relationship and involvement of protein kinase c-dependent and -independent signaling pathways. Biochim Biophys Acta 1993; 1179: 213–223.
   PubMed Web of Science ®Google Scholar
• Fuortes M, Jin W W, Nathan C. Adhesion-dependent protein tyrosine phosphorylation in neutrophils treated with tumor necrosis factor. J Cell Biol 1993; 120: 777–784.
   PubMed Web of Science ®Google Scholar
• Yamada K, Jelsema C L, Beaven M A. Certain inhibitors of protein serine/threonine kinases also inhibit tyrosine phosphorylation of phospholipase Cγ1 and other proteins and reveal distinct roles for tyrosine kinase(s) and protein kinase C in stimulated, rat basophilic RBL-2H3 cells. J Immunol 1992; 149: 1031–1037.
   PubMed Web of Science ®Google Scholar
• Laudanna C, Rossi F, Berton G. Effect of inhibitors of distinct signalling pathways on neutrophil O2-generation in response to tumor necrosis factor-alpha, and antibodies against CD18 and CD11a: evidence for a common and unique pattern of sensitivity to wortmannin and protein tyrosine kinase inhibitors. Biochem Biophys Res Commun 1993; 190: 935–940.
   PubMed Web of Science ®Google Scholar
• Phillips W A, Croatto M, Veis N, Hamilton J A. Protein kinase C has both stimulatory and suppressive effects on macrophage superoxide production. J Cell Physiol 1992; 152: 64–70.
   PubMed Web of Science ®Google Scholar
• Errasfa M, Stern A. Inhibition of epidermal growth factor-dependent protein tyrosine phosphorylation by phorbol myristate acetate is mediated by protein tyrosine phosphatase activity. FEBS Lett 1994; 339: 7–10.
   PubMed Web of Science ®Google Scholar
• Forehand J R, Pabst M J, Phillips W A, Johnston R B Jr. Lipopolysaccharide priming of neutrophils for an enhanced respiratory burst. Role of intracellular free calcium. J Clin Invest 1989; 83: 74–83.
   PubMed Web of Science ®Google Scholar
• McColl S R, Beauseigle D, Gilbert C, Naccache P H. Priming of the human neutrophil respiratory burst by granulocyte-macrophage colony-stimulating factor and tumor necrosis factor-α involves regulation at a post-cell surface receptor level: enhancement of the effect of agents which directly activate G proteins. J Immunol 1990; 145: 3047–3053.
   PubMed Web of Science ®Google Scholar
• Murray H W, Spitalny G L, Nathan C F. Activation of mouse peritoneal macrophages in vitro and in vivo by interferon-γ J Immunol 1985; 134: 1619–1622.
   PubMed Web of Science ®Google Scholar
• Berkow R L, Wang D, Larrick J W, Dodson R W, Howard T H. Enhancement of neutrophil superoxide production by preincubation with recombinant human tumor necrosis factor. J Immunol 1987; 139: 3783–3791.
   PubMed Web of Science ®Google Scholar
• Phillips W A, Hamilton J A. Phorbol ester-stimulated superoxide production by bone marrow-derived macrophages require preexposure to cytokines. J Immunol 1989; 142: 2445–2449.
   PubMed Web of Science ®Google Scholar
• Weinstein S L, Sanghera J S, Lemke K, DeFranco A L, Pelech S L. Bacterial lipopolysaccharide induces tyrosine phosphorylation and activation of mitogen-activated protein kinases in macrophages. J Biol Chem 1992; 267: 14955–14962.
   PubMed Web of Science ®Google Scholar
• Gomez-Cambronero J, Huang C-K, Gomez-Cambronero T M, Waterman W H, Becker E L, Sha'afi R I. Granulocyte-macrophage colony-stimulating factor-induced protein tyrosine phosphorylation of microtubule-associated protein kinase in human neutrophils. Proc Natl Acad Sci USA 1992; 89: 7551–7555.
   PubMed Web of Science ®Google Scholar
• McColl S R, DiPersio J F, Caon A C, Ho P, Naccache P H. Involvement of tyrosine kinases in the activation of human peripheral blood neutrophils by granulocyte-macrophage colony-stimulating factor. Blood 1991; 78: 1842–1852.
   PubMed Web of Science ®Google Scholar
• Berkow R L. Granulocyte-macrophage colony-stimulating factor induces a staurosporine inhibitable tyrosine phosphorylation of unique neutrophil proteins. Blood 1992; 79: 2446–2454.
   PubMed Web of Science ®Google Scholar
• Evans J P, Mire Sluis A R, Hoffbrand A V, Wickremasinghe R G. Binding of G-CSF, GM-CSF, tumor necrosis factor-alpha, and gamma-interferonto cell surface receptors on human myeloid leukemia cells triggers rapid tyrosine and serine phosphorylation of a 75-Kd protein. Blood 1990; 75: 88–95.
   PubMed Web of Science ®Google Scholar
• Tanimura M, Kobuchi H, Utsumi T et al. Neutrophil priming by granulocyte colony stimulating factor and its modulation by protein kinase inhibitors. Biochem Pharmacol 1992; 44: 1045–1052.
   PubMed Web of Science ®Google Scholar
• Zor U, Ferber E, Gergely P, Szucs K, Dombradi V, Goldman R. Reactive oxygen species mediate phorbol ester-regulated tyrosine phosphorylation and phospholipase-a(2) activation—potentiation by vanadate. Biochem J 1993; 295: 879–888.
   PubMed Web of Science ®Google Scholar
• Grinstein S, Furuya W, Lu D J, Mills G B. Vanadate stimulates oxygen consumption and tyrosine phosphorylation in electropermeabilized human neutrophils. J Biol Chem 1990; 265: 318–327.
   PubMed Web of Science ®Google Scholar
• Trudel S, Downey G P, Grinstein S, Paquet M R. Activation of permeabilized HL60 cells by vanadate. Biochem J 1990; 269: 127–131.
   PubMed Web of Science ®Google Scholar
• Yi T L, Willman C L. Cloning of the murine c-fgr proto-oncogene cDNA and induction of c-fgr expression by proliferation and activation factors in normal bone marrow-derived monocytic cells. Oncogene 1989; 4: 1081–1087.
   PubMed Web of Science ®Google Scholar
• Gutkind J S, Robbins K C. Translocation of the FGR protein-tyrosine kinase as a consequence of neutrophil activation. Proc Natl Acad Sci USA 1989; 86: 8783–8787.
   PubMed Web of Science ®Google Scholar
• Grinstein S, Furuya W. Chemoattractant-induced tyrosine phosphorylation and activation of microtubule-associated protein kinase in human neutrophils. J Biol Chem 1992; 267: 18122–18125.
   PubMed Web of Science ®Google Scholar
• Ding A, Sanchez E, Nathan C F. Taxol shares the ability of bacterial lipopolysaccharide to induce tyrosine phosphorylation of microtubule-associated protein kinase. J Immunol 1993; 151: 5596–5602.
   PubMed Web of Science ®Google Scholar
• Huang C-K, Bonak V, Laramee G R, Casnellie J E. Protein tyrosine phosphorylation in rabbit peritoneal neutrophils. Biochem J 1990; 269: 431–436.
   PubMed Web of Science ®Google Scholar
• Liu F, Roth R A. Insulin-stimulated tyrosine phosphorylation of protein kinase C alpha: evidence for direct interaction of the insulin receptor and protein kinase C in cells. Biochem Biophys Res Commun 1994; 200: 1570–1577.
   PubMed Web of Science ®Google Scholar
• Li W, Mischak H, Yu J C et al. Tyrosine phosphorylation of protein kinase c-δ in response to its activation. J Biol Chem 1994; 269: 2349–2352.
   PubMed Web of Science ®Google Scholar
• Heldin C-H. SH2 domains: elements that control protein interactions during signal transduction. Trends Biochem Sci 1991; 16: 450–452.
   PubMed Web of Science ®Google Scholar