Polarization and interaction of adhesion molecules P-selectin glycoprotein ligand 1 and intercellular adhesion molecule 3 with moesin and ezrin in myeloid cells

Blood

Volumn 95, Issue 7, 2000, Pages 2413-2419

  Alonso Lebrero, José L ^b   Serrador, Juan M ^b   Dominguez Jiménez, Carmen ^b   Barreiro, Olga ^b   Luque, Alfonso ^b   Del Pozo, Miguel A ^b   Snapp, Karen ^b   Kansas, Geoffrey ^b   Schwartz Albiez, Reinhard ^b   Furthmayr, Heinz ^b   Lozano, Francisco ^b   Sánchez Madrid, Francisco ^a  

^a HOSPITAL UNIVERSITARIO DE LA PRINCESA   (Spain)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBODY; COMPLEMENT COMPONENT C5A; EZRIN; FORMYLMETHIONYLLEUCYLPHENYLALANINE; GLUTATHIONE TRANSFERASE; HERMES ANTIGEN; INTERCELLULAR ADHESION MOLECULE 3; INTERLEUKIN 15; INTERLEUKIN 8; LEUKOSIALIN; MOESIN; P SELECTIN GLYCOPROTEIN LIGAND 1;

AMINO TERMINAL SEQUENCE; ANTIBODY AFFINITY; ARTICLE; BONE MARROW CELL; CELL STRAIN HL 60; CHEMOTAXIS; CONTROLLED STUDY; CYTOSKELETON; HUMAN; HUMAN CELL; IMMUNOBLOTTING; IMMUNOFLUORESCENCE MICROSCOPY; LEUKOCYTE ACTIVATION; NEUTROPHIL; PRIORITY JOURNAL; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; PSEUDOPODIUM;

EID: 12944283144     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v95.7.2413     Document Type: Article

References (58)

1. Foxman EF, Campbell JJ, Butcher EC. MultiStep navigation and the combinatorial control of leukocyte chemotaxis. J Cell Biol. 1997;139:1349.
2. Shields JM, Haston WS. Behaviour of neutrophil leukocytes in uniform concentrations of chemotactic factors: contraction waves, cell polarity and persistence. J Cell Sci. 1985;74:75.
3. Baggiolini M. Chemokines and leukocyte traffic. Nature. 1998;392:565.
4. Luster AD. Chemokines-chemotactic cytokines that mediate inflammation. New Engl J Med. 1998;338:436.
5. Baggiolini M, Dewald B, Moser B. Interleukin-8 and related chemotactic cytokines: CXC and CC chemokines. Adv Immunol. 1994;55:97.
6. Gerard C, Chemoweth DE, Hugli TE. Response of human neutrophils to C5a: a role for the oligosaccharide moiety of human C5ades Arg74 but not of C5a in biologic activity. J Immunol. 1981; 127:1978.
7. Bajaj MS, Kew RR., Webster RO, Hyers TM. Priming of human neutrophil functions by tumor necrosis factor: enhancement of superoxide anion generation, degranulation, and chemotaxis to chemoattractants C5a and F-Met-Leu-Phe. Inflammation. 1992;16:241.
8. Gerard NP, Gerard C. The chemotactic receptor for human C5a anaphylatoxin. Nature. 1991;349: 614.
9. Murphy PM, Tiffany HL. Cloning of complementary DNA encoding a functional human interleukin-8 receptor. Science. 1991;253:1280.
10. Holmes WE, Lee J, Kuang WJ, Rice GC, Wood WI. Structure and functional expression of a human interleukin-8 receptor. Science. 1991;253: 1278.
11. Kansas GS. Selectins and their ligands: current concepts and controversies. Blood. 1996;88: 3259.
12. Rosen SD, Bertozzi CR. The selectins and their ligands. Curr Opin Cell Biol. 1994;6:663.
13. Sako D, Chang XJ, Barone KM, et al. Expression cloning of a functional glycoprotein ligand for P-selectin. Cell. 1993;75:1179.
14. Moore KL, Patel KD, Bruehl RE, et al. P-selectin glycoprotein ligand-1 mediates rolling of human neutrophils on P-selectin. J Cell Biol. 1995;128: 661.
15. Laszik Z, Jansen PJ, Cummings RD, et al. P-selectin glycoprotein ligand-1 is broadly expressed in cells of myeloid, lymphoid and dendritic lineage and in some non-hematopoietic cells. Blood. 1996;88:3010.
16. McEver R, Cummings R. Role of PSGL-1 binding to selectins in leukocyte recruitment. J Clin Invest. 1997;100:485.
17. Snapp KR, Ding H, Atkins K, Warnke R, Luscinskas F, Kansas GS. A novel P-selectin glycoprotein ligand-1 monoclonal antibody recognizes an epitope within the tyrosine sulphate motif of human PSGL-1 and blocks recognition of both P- and L- selectin. Blood. 1998;91:154.
18. del Pozo MA, Sánchez-Mateos P, Nieto M, Sánchez-Madrid F. Chemokines regulate cellular polarization and adhesion receptor redistribution lymphocyte interaction with endothelium and extracellular matrix: involvement of cAMP signaling pathways. J Cell Biol. 1995;131:495.
19. Nieto M, Navarro F, Pérez-Villar JJ, et al. Roles of chemokines and receptor polarization in NK-target cell interactions. J Immunol. 1998;161:3330.
20. Vicente-Manzanares M, Montoya MC, Mellado M, et al. The chemokine SDF-1α triggers a chemotactic response and induces cell polarization in human B lymphocytes. Eur J Immunol. 1998;28: 2197.
21. Lorant DE, McEver RP, McIntyre TM, Moore KL, Prescott SM, Zimmerman GA. Activation of polymorphonuclear leukocytes reduces their adhesion to P-selectin and causes redistribution of ligands for P-selectin on their surfaces. J Clin Invest. 1995;96:171.
22. Doré M, Burns AR, Hughes BJ, Entman ML, Smith CW. Chemoattractant-induced changes in surface expression and redistribution of a functional ligand for P-selectin on neutrophils. Blood. 1996;87:2029.
23. del Pozo MA, Cabanas C, Montoya M, Ager A, Sénchez-Mateos P, Sánchez-Madrid F. ICAMs redistributed by chemokines to cellular uropods as a mechanism for recruitment of T lymphocytes. J Cell Biol. 1997;137:493.
24. Serrador JM, Alonso-Lebrero JL, del Pozo MA, et al. Moesin interacts with the cytoplasmic region of intercellular adhesion molecule-3 and is redistributed to the uropod of T lymphocytes during cell polarization. J Cell Biol. 1997;138:1409.
25. Serraoof JM, Nieto M, Alonso-Lebrero JL, et al. CD43 interacts with moesin and ezrin and regulates its redistribution to the uropods of T lymphocytes at the cell-cell contacts. Blood. 1998;91: 4632.
26. Tsukita SA, Yonemura S, Tsukita SH. ERM (ezrin/ radixin/moesin) family: from cytoskeleton to signal transduction. Curr Opin Cell Biol. 1997;9:70.
27. Vaheri A, Carpén O, Heiska L, et al. The ezrin protein family: membrane-cytoskeleton interactions and disease associations. Curr Opin Cell Biol. 1997;9:659.
28. Bretscher A. Regulation of cortical structure by the ezrin-radixin-moesin protein family. Curr Opin Cell Biol. 1999;11:109.
29. Amieva MR, Furthmayr H. Subcellular localization of moesin in dynamic filopodia, retraction fibers, and other structures involved in substrate exploration, attachment and cell-cell contacts. Exp Cell Res. 1995;219:180.
30. Schwartz-Albiez R, Merling A, Spring H, Möller P, Korenz K. Differential expression of the microspike-associate protein moesin in human tissues. Eur J Cell Biol. 1995;67:189.
31. Berryman M, Gary R, Bretscher A. Ezrin oligomers are major cytoskeletal components of placental microvilli: a proposal for their involvement in cortical morphogenesis. J Cell Biol. 1995;131: 1231.
32. Fath KR, Burgess DR. Not actin alone. Curr Biol. 1995;5:591.
33. Paglini G, Kunda P, Quiroga S, Kosik K. Caceres AJ. Suppression of radixin and moesin alters growth cone morphology, motility, and process formation in primary cultured neurons. J Cell Biol. 1998;143:443
34. Pestonjamasp K, Amieva MR, Strassel CP, Nauseef WM, Furthmayr H, Luna EJ. Moesin, ezrin and p205 are actin-binding proteins associated with neutrophil plasma membranes. Mol Biol Cell. 1995;6:247.
35. Lankes W, Griesmacher A, Grunwald J, Schwartz-Albiez R, Keller R. A heparin-binding protein involved in inhibition of smooth-muscle cell proliferation. Biochem J. 1988;251:831.
36. Campanero MR, Pulido R, Alonso JL, et al. Down-regulation by tumor necrosis factor-α of neutrophil cell surface expression of the sialophorin CD43 and the hyaluronate receptor CD44 though a proteolytic mechanism. Eur J Immunol. 1991;21:3045.
37. Campanero MR, del Pozo MA, Arroyo AG, et al. ICAM-3 interacts with LFA-1 and regulates the LFA-1/ICAM-1 cell adhesion pathway. J Cell Biol. 1993;123:1007.
38. Lankes W, Furthmayr H. Moesin: a member of the protein 4.1-talin-ezrin family of proteins. Proc Natl Acad Sci U S A. 1991;88:8297.
39. Dejana E, Colella S, Languino R, Balconi G, Corbascio GC, Marchisio PC. Fibrinogen induces adhesion, spreading and microfilament organization of human endothelial cells in vitro. J Cell Biol. 1987;104:1403.
40. Huang L, Won TYW, Lin RCC, Furthmayr H. Replacement of 558 threonine, a critical site of phosphorylation of moesin in vivo, with aspartate activates F-actin binding of moesin: regulation by conformational change. J Biol Chem. 1999;274: 12,803.
41. Nakamura F, Huang L, Pestonjamasp K, Luna EJ, Furthmayr H. Regulation of F-actin binding of platelet moesin in vitro by both phosphorylation of threonine 558 and polyphosphoinositides. Mol Biol Cell. 1999;10:2669.
42. Bevilacqua MP. Endothelial-leukocyte adhesion molecules. Ann Rev Immunol. 1993;11:767.
43. Adams DH, Shaw S. Leukocyle-endothelial interactions and regulation of leukocyte migration. Lancet. 1994;343:831.
44. Finger EB, Puri KD, Alon R, Lawrence MB, Von Adrian UH, Springer TA. Adhesion through L-selectin requires a threshold hydrodynamic shear. Nature. 1996;379:266.
45. Walcheck B, Moore KL, McEver RP, Kishimoto TK. Neutrophil-neutrophil interactions under hydrodynamic shear stress involve L-selectin and PSGL-1. J Clin Invest. 1996;98:1081.
46. von Andrian UH, Hasslen SR, Nelson RD, Erlandsen SL, Butcher EC. A central role for microvillous receptor presentation in leukocyte adhesion under flow. Cell. 1995;82:989.
47. McFarland W. Microspikes on the lymphocyte uropod. Science. 1969;163:818.
48. Feng D, Nagy JA, Pyne K, Dvorak HF, Dvorak AM. Neutrophils emigrate from venules by a transendothelial cell pathway in response to fMLP.J Exp Med. 1998;187:903.
49. Matsui T, Maeda M, Doi Y, et al. Rho kinase phosphorylates COOH-terminal threonine of ezrin/ radixin/moesin (ERM) proteins and regulates their head-to-tail association. J Cell Biol. 1998; 140:647.
50. Tsukita SA, Oishi K, Sato N, Sagara J, Kawai A, Tsukita SH. ERM family members as molecular linkers between the cell surface glycoprotein CD44 and actin-based cytoskeletons. J Cell Biol. 1994;126:391.
51. Heiander TS, Carpén O, Turunen O, Kovanen PE, Vaheri A, Timonen T. ICAM-2 redistributed by ezrin as a target for killer cells. Nature. 1996;382: 265.
52. Heiska L, Alfthan K, Gronholm M, Vilja P, Vaheri A, Carpen O. Association of ezrin with intercellular adhesion molecule-1 and -2 (ICAM-1 and ICAM-2). J Biol Chem. 1998;273:21,893.
53. Yonemura S, Hirao M, Doi M, et al. Ezrin/radixin/ moesin (ERM) proteins bind to a positively charged amino acid cluster in the juxta-membrane cytoplasmic domain of CD44, CD43, and ICAM-2. J Cell Biol. 1998;140:885.
54. Pietromonaco SF, Simons PC, Altman A, Laurence E. Protein kinase C-6 phosphorylation of moesin in the actin-binding sequence. J Biol Chem 1998;273:7594.
55. Hirao M, Sato N, Kondo T, et al. Regulation mechanism of ERM (ezrin/radixin/moesin) protein/plasma membrane association: possible involvement of phosphatidylinositol turnover and Rho-dependent signaling pathway. J Cell Biol. 1996;135:37.
56. Gautreau A, Poullet P, Louvard D, Arpin M. Ezrin, a plasma membrane-microfilament linker, signals cell survival through the phosphatidylinositol 3-kinase/Akt pathway. Proc Natl Acad Sci U S A. 1999;96:7300.
57. Reczek D, Berryman M, Bretscher A. Identification of EBP50: a PDZ-containing phosphoprotein that associates with members of the ezrin-radixinmoesin family. J Cell Biol. 1997;139:169.
58. Cao TT, Deacon HW, Reczek D, Bretscher A, von Zasfrow M. A kinase-regulated PDZ-domain interaction controls endocytic sorting of the β2-adrenergic receptor. Nature. 1999;401:286.