Lymphocyte migration into a tissue depends on properties of both the l
ymphocyte and the tissue's vascular endothelium. The central nervous s
ystem (CNS) possesses a specialized microvasculature and lymphocytes a
ppear to enter the CNS less readily than peripheral tissues. We invest
igated whether those lymphocytes that interact with the CNS, as repres
ented by cerebrospinal fluid (CSF)-derived lymphocytes, express adhesi
ve properties distinct from peripheral blood lymphocytes (PBLs). Adhes
ion of human lymphocytes to bovine endothelial cell monolayers was qua
ntitated microscopically. A greater number of PBLs adhered to aortic t
han to retinal endothelial cell cultures (e.g., 10.9 +/- 0.6 and 4.5 /- 0.2, respectively; P = 0.0023). Preincubation of either endothelial
cell type with tumor necrosis factor-alpha (TNF-alpha) enhanced lymph
ocyte adhesion. Activation of PBLs with concanavalin A or phytohemaggl
utinin increased endothelial cell adhesion and the effect was additive
with that of TNF-alpha. The number of CSF lymphocytes adhering to end
othelial cell cultures (retinal, 67.5 +/- 9.0; aortic, 83.7 +/- 10.6)
was more than 10 times the number of PBLs (retinal, 5.4 +/- 0.8; aorti
c, 8.0 +/- 1.3; P < 0.0001), CSF lymphocytes did not, however, adhere
preferentially to CNS-derived endothelial cell cultures. These results
suggest that CSF may be enriched, compared with peripheral blood, in
its content of surveillance lymphocytes, but that these cells might en
ter target tissues nonspecifically.