TY - JOUR
T1 - Cytohesin-1 regulates beta-2 integrin-mediated adhesion through both ARF-GEF function and interaction with LFA-1
AU - Geiger, C
AU - Nagel, W
AU - Boehm, T
AU - van Kooyk, Y
AU - Figdor, C G
AU - Kremmer, E
AU - Hogg, N
AU - Zeitlmann, L
AU - Dierks, H
AU - Weber, K S
AU - Kolanus, W
PY - 2000/6/1
Y1 - 2000/6/1
N2 - Intracellular signaling pathways, which regulate the interactions of integrins with their ligands, affect a wide variety of biological functions. Here we provide evidence of how cytohesin-1, an integrin-binding protein and guanine-nucleotide exchange factor (GEF) for ARF GTPases, regulates cell adhesion. Mutational analyses of the beta-2 cytoplasmic domain revealed that the adhesive function of LFA-1 depends on its interaction with cytohesin-1, unless the integrin is activated by exogenous divalent cations. Secondly, cytohesin-1 induces expression of an extracellular activation epitope of LFA-1, and the exchange factor function is not essential for this activity. In contrast, LFA-1-mediated cell adhesion and spreading on intercellular cell adhesion molecule 1 is strongly inhibited by a cytohesin-1 mutant, which fails to catalyze ARF GDP-GTP exchange in vitro. Thus, cytohesin-1 is involved in the activation of LFA-1, most probably through direct interaction with the integrin, and induces cell spreading by its ARF-GEF activity. We therefore propose that both direct regulation of the integrin and concomitant changes in the membrane topology of adherent T cells are modulated by dissectable functions of cytohesin-1.
AB - Intracellular signaling pathways, which regulate the interactions of integrins with their ligands, affect a wide variety of biological functions. Here we provide evidence of how cytohesin-1, an integrin-binding protein and guanine-nucleotide exchange factor (GEF) for ARF GTPases, regulates cell adhesion. Mutational analyses of the beta-2 cytoplasmic domain revealed that the adhesive function of LFA-1 depends on its interaction with cytohesin-1, unless the integrin is activated by exogenous divalent cations. Secondly, cytohesin-1 induces expression of an extracellular activation epitope of LFA-1, and the exchange factor function is not essential for this activity. In contrast, LFA-1-mediated cell adhesion and spreading on intercellular cell adhesion molecule 1 is strongly inhibited by a cytohesin-1 mutant, which fails to catalyze ARF GDP-GTP exchange in vitro. Thus, cytohesin-1 is involved in the activation of LFA-1, most probably through direct interaction with the integrin, and induces cell spreading by its ARF-GEF activity. We therefore propose that both direct regulation of the integrin and concomitant changes in the membrane topology of adherent T cells are modulated by dissectable functions of cytohesin-1.
KW - ADP-Ribosylation Factors/physiology
KW - Animals
KW - CD18 Antigens/physiology
KW - Cell Adhesion/physiology
KW - Cell Adhesion Molecules/genetics
KW - Cell Size
KW - Epitopes/chemistry
KW - Guanine Nucleotide Exchange Factors
KW - Guanosine Diphosphate/metabolism
KW - Guanosine Triphosphate/metabolism
KW - HeLa Cells
KW - Humans
KW - Intercellular Adhesion Molecule-1/physiology
KW - Lymphocyte Function-Associated Antigen-1/physiology
KW - Macromolecular Substances
KW - Mice
KW - Models, Molecular
KW - Rats
KW - Recombinant Fusion Proteins/physiology
KW - T-Lymphocytes/cytology
KW - Two-Hybrid System Techniques
U2 - 10.1093/emboj/19.11.2525
DO - 10.1093/emboj/19.11.2525
M3 - Article
C2 - 10835351
SN - 0261-4189
VL - 19
SP - 2525
EP - 2536
JO - EMBO Journal
JF - EMBO Journal
IS - 11
ER -