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*
Laboratory of Molecular and Cellular Recognition, Osaka University Graduate School of Medicine; and
Institute for Molecular and Cellular Biology, Osaka University, Suita, Japan
High endothelial venule (HEV) cells support lymphocyte migration
from the peripheral blood into secondary lymphoid tissues. Using gene
expression profiling of mucosal addressin cell adhesion
molecule-1+ mesenteric lymph node HEV cells by quantitative
3'-cDNA collection, we have identified a leucine-rich protein, named
leucine-rich HEV glycoprotein (LRHG) that is selectively expressed in
these cells. Northern blot analysis revealed that LRHG mRNA is
1.3
kb and is expressed in lymph nodes, liver, and heart. In situ
hybridization analysis demonstrated that the mRNA expression in lymph
nodes is strictly restricted to the HEV cells, and immunofluorescence
analysis with polyclonal Abs against LRHG indicated that the LRHG
protein is localized mainly to HEV cells and possibly to some lymphoid
cells surrounding the HEVs. LRHG cDNA encodes a 342-aa protein
containing 8 tandem leucine-rich repeats of 24 aa each and has high
homology to human leucine-rich
2-glycoprotein. Similar
to some other leucine-rich repeat protein family members, LRHG can bind
extracellular matrix proteins that are expressed on the basal lamina of
HEVs, such as fibronectin, collagen IV, and laminin. In addition, LRHG
binds TGF-
. These results suggest that LRHG is likely to be
multifunctional in that it may capture TGF-
and/or other related
humoral factors to modulate cell adhesion locally and may also be
involved in the adhesion of HEV cells to the surrounding basal
lamina.
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