VLA family in rheumatoid arthritis: evidence forin vivoregulated adhesion of synovial fluid T cells to fibronectin through VLA-5 integrin

Abstract

Adhesion of T cells to extracellular matrix (ECM) proteins through VLA integrin receptors is crucial for lymphocyte trafficking, tissue localization and inflammatory function. We have investigated the expression of different VLA integrins (VLA‐l‐5) on peripheral blood (PB) and synovial fluid (SF) T lymphocytes from patients with rheumatoid arthritis (RA). Their expression on different cell types from synovial membrane (SM) is also reported. The role of VLA‐4 fibronectin (FN) receptors in the interaction of activated SF T cells from RA patients with a 38‐kD fragment of FN has been previously demonstrated. Here we have focused functional studies on VLA‐5 as an alternative FN receptor for RA T cells. A significant higher proportion of SF T cells were able to bind to an 80‐kD fragment of FN, containing the Arg–Gly–Asp (RGD) cell binding site, compared with PB T cells. This attachment was almost completely inhibited by anti‐VLA‐5 MoAbs as well as by RGD peptides. This enhanced capability by SFT cells appears to be independent of the level of the surface expression of the receptor and correlates better with their activation state as determined by the expression of the activation molecule AIM (CD69). The evidence for the expression of VLA heterodimers on both SF and SM cells from R.A patients suggests the possible implication of ECM proteins in mediating and perpetuating inflammation in vivo.