Polarization and interaction of adhesion molecules P-selectin glycoprotein ligand 1 and intercellular adhesion molecule 3 with moesin and ezrin in myeloid cells.
Polarization and interaction of adhesion molecules P-selectin glycoprotein ligand 1 and intercellular adhesion molecule 3 with moesin and ezrin in myeloid cells.
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骨髓细胞中粘附分子 P-选择素糖蛋白配体 1 和细胞间粘附分子 3 的极化和与 moesin 和 ezrin 的相互作用。
DOI:
10.1182/blood.v95.7.2413
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发表时间:
2000
期刊:
影响因子:
20.3
通讯作者:
F. Sánchez‐Madrid
中科院分区:
文献类型:
--
作者:
J. Alonso;J. Serrador;C. Domı́nguez;O. Barreiro;A. Luque;M. A. del Pozo;K. Snapp;G. Kansas;R. Schwartz;H. Furthmayr;F. Lozano;F. Sánchez‐Madrid
In response to the chemoattractants interleukin 8, C5a, N-formyl-methionyl-leucyl-phenylalanine, and interleukin 15, adhesion molecules P-selectin glycoprotein ligand 1 (PSGL-1), intercellular adhesion molecule 3 (ICAM-3), CD43, and CD44 are redistributed to a newly formed uropod in human neutrophils. The adhesion molecules PSGL-1 and ICAM-3 were found to colocalize with the cytoskeletal protein moesin in the uropod of stimulated neutrophils. Interaction of PSGL-1 with moesin was shown in HL-60 cell lysates by isolating a complex with glutathione S-transferase fusions of the cytoplasmic domain of PSGL-1. Bands of 78- and 81-kd were identified as moesin and ezrin by Western blot analysis. ICAM-3 and moesin also coeluted from neutrophil lysates with an anti-ICAM-3 immunoaffinity assay. Direct interaction of the cytoplasmic domains of ICAM-3 and PSGL-1 with the amino-terminal domain of recombinant moesin was demonstrated by protein-protein binding assays. These results suggest that the redistribution of PSGL-1 and its association with intracellular molecules, including the ezrin-radixin-moesin actin-binding proteins, regulate functions mediated by PSGL-1 in leukocytes stimulated by chemoattractants.
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影响因子:
20.3
作者:
Laszik, Z;Jansen, PJ;Moore, KL
通讯作者:
Moore, KL
影响因子:
7.5
作者:
ROSEN, SD;BERTOZZI, CR
通讯作者:
BERTOZZI, CR
DOI:
--
发表时间:
1981
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Gerard,C;Chenoweth,DE;Hugli,TE
通讯作者:
Hugli,TE
影响因子:
3.3
作者:
Nakamura, F;Huang, LQ;Furthmayr, H
通讯作者:
Furthmayr, H
影响因子:
7.5
作者:
Bretscher, A
通讯作者:
Bretscher, A