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Blood, 1 August 2001, Vol. 98, No. 3, pp. 688-695
IMMUNOBIOLOGY
Transendothelial migration of lymphocytes across high endothelial
venules into lymph nodes is affected by metalloproteinases
Christelle Faveeuw,
Graham Preece, and
Ann Ager
From the Division of Cellular Immunology, National
Institute for Medical Research, The Ridgeway, Mill Hill, London,
United Kingdom.
The migration of lymphocytes from the bloodstream into lymph nodes
(LNs) via high endothelial venules (HEVs) is a prerequisite for the
detection of processed antigen on mature dendritic cells and the
initiation of immune responses. The capture and arrest of lymphocytes
from flowing blood is mediated by the multistep adhesion cascade, but
the mechanisms that lymphocytes use to penetrate the endothelial lining
and the basement membrane of HEVs are poorly understood. Matrix
metalloproteinases (MMPs) control the metastatic spread of tumor cells
by regulating the penetration blood vessel basement membranes. In this
study, synthetic and natural inhibitors were used to determine the role
of MMPs and MMP-related enzymes in regulating lymphocyte extravasation
in mice. Mice were treated systemically with the hydroxamate-based MMP
inhibitor Ro 31-9790 and plasma monitored for effective
levels of Ro 31-9790, which block shedding of L-selectin. The total
numbers of lymphocytes recruited into LNs were not altered, but
L-selectin levels were higher in mice treated with Ro
31-9790. A reduced number of lymphocytes completed diapedesis and
there was an increase in the number of lymphocytes in the endothelial
cell lining, rather than the lumen or the basement membrane of HEVs.
Lymphocyte migration and L-selectin expression in the spleen were not
altered by Ro 31-9790 treatment. Two MMP inhibitors,
TIMP1 and Ro 32-1541, did not block L-selectin shedding and had
no effect on lymphocyte migration across HEVs. These results suggest
that metalloproteinase activity is required for lymphocyte
transmigration across HEVs into LNs and provide evidence for the
concept that metalloproteinases are important players in some forms of
transendothelial migration.

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