Re. Mebius et al., DEVELOPMENTAL REGULATION OF VASCULAR ADDRESSIN EXPRESSION - A POSSIBLE ROLE FOR SITE-ASSOCIATED ENVIRONMENTS, International immunology, 5(5), 1993, pp. 443-449
Tissue selective traffic of lymphocytes into different lymphoid organs
is mediated by adherence of blood borne lymphocytes to specialized en
dothelial cells lining the high endothelial venules (HEV) in lymphoid
organs. Lymphocytes discriminate between HEV in peripheral lymph nodes
and in mucosal lymphoid tissues by means of membrane associated lymph
ocyte homing receptors adhering to their putative HEV ligands, the vas
cular addressins. The expression of particular vascular addressins on
HEV is site- or tissue-selective and may be directed by factors unique
to a specific location or lymph node environment. In this study we in
vestigated the impact of regional environments on lymph node HEV diffe
rentiation and function. Experimentally, this problem was approached b
y the transplantation of lymph nodes from one region to a second regio
n. The sites selected for receipt of tissues were the mesentery, a muc
osal site, and the popliteal fossa, a peripheral site. We found that t
he phenotype of lymph node HEV following transplantation was influence
d by both donor age and transplantation site. The transplantation site
could influence vascular addressin expression, when tissues were obta
ined from late fetal or early neonatal donors and not when obtained fr
om adult donors. Transplanted adult tissues retained their pre-transpl
antation vascular addressin expression phenotype regardless of transpl
antation site. Thus the endothelium within adult lymph nodes may be co
mmitted to expression of a particular addressin or addressins during l
ymph node development. It is also possible that regulatory cells or st
ructures present within lymph nodes at the time of transplantation dir
ect vascular addressin expression following tissue engraftment. These
studies show that regional environments of the lymph nodes could play
a role in HEV differentiation and function during lymph node developme
nt.