DIVALENT-CATIONS AND LIGANDS INDUCE CONFORMATIONAL-CHANGES THAT ARE HIGHLY DIVERGENT AMONG BETA(1) INTEGRINS

Citation
G. Bazzoni et al., DIVALENT-CATIONS AND LIGANDS INDUCE CONFORMATIONAL-CHANGES THAT ARE HIGHLY DIVERGENT AMONG BETA(1) INTEGRINS, The Journal of biological chemistry, 273(12), 1998, pp. 6670-6678
Citations number
73
Categorie Soggetti
Biology
ISSN journal
00219258
Volume
273
Issue
12
Year of publication
1998
Pages
6670 - 6678
Database
ISI
SICI code
0021-9258(1998)273:12<6670:DALICT>2.0.ZU;2-5
Abstract
Here we show striking differences in conformational regulation among b eta(1) integrins. Upon manganese stimulation, a beta(1) epitope define d by monoclonal antibody (mAb) 9EG7 was induced strongly (on alpha(4) beta(1)), moderately (on alpha(5) beta(1)), weakly (on alpha(2) beta(1 )), or was scarcely detectable (on alpha(6) beta(1) and alpha(3) beta( 1)). Comparable results were seen for the beta(1) epitope defined by m Ab 15/7. Likewise, soluble ligands caused strong (alpha(4) beta(1)), m oderate (alpha(5) beta(1)), weak (alpha(2) beta(1), alpha(6) beta(1)), Or minimal (alpha(3) beta(1)) induction of the 9EG7 epitope. Exchange or deletion of alpha chain cytoplasmic tails did not alter Mn2+-induc ed 9EG7 epitope levels. Upon removal of calcium by EGTA or EDTA, the h ierarchy of 9EG7 epitope induction was similar (alpha(5) beta(1) > alp ha(2) beta(1) > alpha(6) beta(1) > alpha(3) beta(1)), except that EGTA reduced rather than induced 9EG7 expression on alpha(4) beta(1). Thus in contrast to other beta(1) integrins, calcium uniquely supports con stitutive expression of the 9EG7 epitope on alpha(4) beta(1). Likewise , calcium supported vascular cell adhesion molecule-stimulated 9EG7 ap pearance on alpha(4) beta(1), whereas calcium inhibited ligand-induced 9EG7 epitope on other integrins. Constitutive expression of 9EG7 on a lpha(4) beta(1) was eliminated by a D698E mutation in alpha(4), sugges ting that Asp-698 may play a key role in maintaining atypical alpha(4) beta(1) response to calcium. In conclusion, our results (i) demonstra te that mAb such as 9EG7 and 15/7 have limited diagnostic utility as r eporters of ligand or Mn2+ occupancy for beta(1) integrins, (ii) indic ate pronounced differences in conformational flexibilities (alpha(4) b eta(1) > alpha(5) beta(1) > alpha(2) beta(1) > alpha(6) beta(1) > alph a(3) beta(1)), (iii) allow us to hypothesize that beta(1) integrins ma y differ markedly in conformation-dependent inside-out signaling, and (iv) have uncovered an atypical alpha(4) beta(1) response to calcium t hat requires alpha(4) Asp-698.