Brain and retinal endothelial cells (EC) form the blood-brain and vasc
ular blood-retinal barriers, respectively, and are believed to play a
role in mediating T cell responses in the central nervous system. In t
his study, Lewis rat retinal and brain EC grown in vitro were capable
of expressing MHC class II I-A but not I-E molecules following treatme
nt with interferon-gamma. In the presence of their antigen, CD4(+) ant
igen-specific T cells were able to mediate lysis of retinal EC monolay
ers to a similar extent as brain EC. T cell proliferation was poorly s
upported by confluent retinal or brain EC monolayers, but subconfluent
EC monolayers supported proliferation in a MHC class II (I-A)-restric
ted manner (P < 0.001). Exposure of T cells to confluent retinal EC mo
nolayers resulted in them becoming less responsive to subsequent antig
en presentation by thymocytes. Conversely, pre-exposure with subconflu
ent EC had no such effect. These results suggest that a non-proliferat
ing EC monolayer is able to downregulate T cell responsiveness which m
ay have important implications during lymphocyte traffic across the bl
ood-tissue barriers of the central nervous system.