Alpha9beta1 integrin in melanoma cells can signal different adhesion states for migration and anchorage

Magnus C Lydolph; Marie Morgan-Fisher; Anette M Høye; John R Couchman; Ulla M Wewer; Atsuko Yoneda

doi:10.1016/j.yexcr.2009.09.022

Alpha9beta1 integrin in melanoma cells can signal different adhesion states for migration and anchorage

Magnus C Lydolph, Marie Morgan-Fisher, Anette M Høye, John R Couchman, Ulla M Wewer, Atsuko Yoneda

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

41 Citationer (Scopus)

Abstract

Udgivelsesdato: 2009-Nov-15

Originalsprog	Engelsk
Tidsskrift	Experimental Cell Research
Vol/bind	315
Udgave nummer	19
Sider (fra-til)	3312-24
Antal sider	12
ISSN	0014-4827
DOI	https://doi.org/10.1016/j.yexcr.2009.09.022
Status	Udgivet - 2009

Adgang til dokumentet

10.1016/j.yexcr.2009.09.022

Citationsformater

@article{5aa1dc70d5ce11dea1f3000ea68e967b,

title = "Alpha9beta1 integrin in melanoma cells can signal different adhesion states for migration and anchorage",

abstract = "Cell surface integrins are the primary receptors for cell migration on extracellular matrix, and exist in several activation states regulated in part by ectodomain conformation. The alpha9 integrin subunit, which pairs only with beta1, has specific roles in the immune system and may regulate cell migration. Melanoma cells express abundant alpha9beta1 integrin, and its role in cell migration was assessed. Ligands derived from Tenascin-C and ADAM12 supported alpha9beta1 integrin-mediated cell attachment and GTP-Rac dependent migration, but not focal adhesion formation. Manganese ions induced alpha9beta1 integrin- and Rho kinase-dependent focal adhesion and stress fibre formation, suggesting that the activation status of alpha9beta1 integrin was altered. The effect of manganese ions in promoting focal adhesion formation was reproduced by beta1 integrin activating antibody. The alpha9beta1 integrin translocated to focal adhesions, where active beta1 integrin was also detected by conformation-specific antibodies. Focal adhesion assembly was commensurate with reduced cell migration. Endogenous alpha9beta1 integrin-mediated adhesion was sensitive to the PP1 chemical inhibitor and an inhibitor of endosomal vesicle recycling, but not inhibitors of protein kinase C or the small GTPase Rho. Our results demonstrated that although alpha9beta1 integrin can induce and localise to focal adhesions in a high activation state, its intermediate activity state normally supports cell adhesion consistent with migration.",

author = "Lydolph, {Magnus C} and Marie Morgan-Fisher and H{\o}ye, {Anette M} and Couchman, {John R} and Wewer, {Ulla M} and Atsuko Yoneda",

year = "2009",

doi = "10.1016/j.yexcr.2009.09.022",

language = "English",

volume = "315",

pages = "3312--24",

journal = "Experimental Cell Research",

issn = "0014-4827",

publisher = "Academic Press",

number = "19",

}

TY - JOUR

T1 - Alpha9beta1 integrin in melanoma cells can signal different adhesion states for migration and anchorage

AU - Lydolph, Magnus C

AU - Morgan-Fisher, Marie

AU - Høye, Anette M

AU - Couchman, John R

AU - Wewer, Ulla M

AU - Yoneda, Atsuko

PY - 2009

Y1 - 2009

N2 - Cell surface integrins are the primary receptors for cell migration on extracellular matrix, and exist in several activation states regulated in part by ectodomain conformation. The alpha9 integrin subunit, which pairs only with beta1, has specific roles in the immune system and may regulate cell migration. Melanoma cells express abundant alpha9beta1 integrin, and its role in cell migration was assessed. Ligands derived from Tenascin-C and ADAM12 supported alpha9beta1 integrin-mediated cell attachment and GTP-Rac dependent migration, but not focal adhesion formation. Manganese ions induced alpha9beta1 integrin- and Rho kinase-dependent focal adhesion and stress fibre formation, suggesting that the activation status of alpha9beta1 integrin was altered. The effect of manganese ions in promoting focal adhesion formation was reproduced by beta1 integrin activating antibody. The alpha9beta1 integrin translocated to focal adhesions, where active beta1 integrin was also detected by conformation-specific antibodies. Focal adhesion assembly was commensurate with reduced cell migration. Endogenous alpha9beta1 integrin-mediated adhesion was sensitive to the PP1 chemical inhibitor and an inhibitor of endosomal vesicle recycling, but not inhibitors of protein kinase C or the small GTPase Rho. Our results demonstrated that although alpha9beta1 integrin can induce and localise to focal adhesions in a high activation state, its intermediate activity state normally supports cell adhesion consistent with migration.

AB - Cell surface integrins are the primary receptors for cell migration on extracellular matrix, and exist in several activation states regulated in part by ectodomain conformation. The alpha9 integrin subunit, which pairs only with beta1, has specific roles in the immune system and may regulate cell migration. Melanoma cells express abundant alpha9beta1 integrin, and its role in cell migration was assessed. Ligands derived from Tenascin-C and ADAM12 supported alpha9beta1 integrin-mediated cell attachment and GTP-Rac dependent migration, but not focal adhesion formation. Manganese ions induced alpha9beta1 integrin- and Rho kinase-dependent focal adhesion and stress fibre formation, suggesting that the activation status of alpha9beta1 integrin was altered. The effect of manganese ions in promoting focal adhesion formation was reproduced by beta1 integrin activating antibody. The alpha9beta1 integrin translocated to focal adhesions, where active beta1 integrin was also detected by conformation-specific antibodies. Focal adhesion assembly was commensurate with reduced cell migration. Endogenous alpha9beta1 integrin-mediated adhesion was sensitive to the PP1 chemical inhibitor and an inhibitor of endosomal vesicle recycling, but not inhibitors of protein kinase C or the small GTPase Rho. Our results demonstrated that although alpha9beta1 integrin can induce and localise to focal adhesions in a high activation state, its intermediate activity state normally supports cell adhesion consistent with migration.

U2 - 10.1016/j.yexcr.2009.09.022

DO - 10.1016/j.yexcr.2009.09.022

M3 - Journal article

C2 - 19796635

VL - 315

SP - 3312

EP - 3324

JO - Experimental Cell Research

JF - Experimental Cell Research

SN - 0014-4827

IS - 19

ER -