EXPRESSION OF FUSION REGULATORY PROTEINS (FRPS) ON HUMAN PERIPHERAL-BLOOD MONOCYTES - INDUCTION OF HOMOTYPIC CELL-AGGREGATION AND FORMATIONOF MULTINUCLEATED GIANT-CELLS BY ANTI-FRP-1 MONOCLONAL-ANTIBODIES
M. Ito et al., EXPRESSION OF FUSION REGULATORY PROTEINS (FRPS) ON HUMAN PERIPHERAL-BLOOD MONOCYTES - INDUCTION OF HOMOTYPIC CELL-AGGREGATION AND FORMATIONOF MULTINUCLEATED GIANT-CELLS BY ANTI-FRP-1 MONOCLONAL-ANTIBODIES, The Journal of immunology, 153(7), 1994, pp. 3256-3266
Fusion regulatory proteins (FRPs) are newly defined cell surface molec
ules that enhance and/or induce virus-mediated cell fusion. Anti-FRP-1
Abs reacted with all of the established cells derived from humans and
monkeys, whereas FRPs were found to be selectively expressed on a fra
ction of monocytes in human PBMCs. Granulocytes expressed no FRP-1 mol
ecules, but approximately 18% of granulocytes expressed FRP-2 molecule
s. Alveolar macrophages also expressed FRP-1 molecules. FRP-1 expressi
on was enhanced by culture of monocytes, but CD14 expression was not i
nfluenced by cultivation. Anti-FRP-1 Abs induced homotypic cell aggreg
ation and multinucleated giant cell formation of monocytes. Anti-beta
2 integrin Ab blocked anti-FRP-1 Ab-induced cell aggregation, and anti
-beta 1 integrin Ab and fibronectin inhibited anti-FRP-1 Ab-induced po
lykaryocyte formation. There was no competitive binding to monocytes b
etween anti-FRP-1 Ab and anti-beta 1 or anti-beta 2 integrin Ab or fib
ronectin. Furthermore, there was no enhancement of beta 1 and beta 2 i
ntegrin expression by anti-FRP-1 Ab on monocytes. These findings sugge
st that anti-FRP-1 Ab activated integrin systems, and that the functio
ns of anti-FRP-1 Ab were demonstrated through the activated integrin s
ystems. Furthermore, it is inferred that integrin systems are involved
in polykaryocyte formation of monocytes.