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J Biol Chem, Vol. 273, Issue 32, 20677-20684, August 7, 1998
From the Matrix metalloproteinases (MMPs) are involved in
the remodeling of connective tissue as well as in disease states
associated with acute and chronic inflammation or tumoral metastatic
processes. Despite detailed and extensive studies of the mechanisms of
lymphocyte extravasation, remarkably little is known about the
expression and regulation of metalloproteinases involved in the
migratory process. By using zymography and reverse
transcription-polymerase chain reaction experiments, we have
demonstrated that Epstein-Barr virus-immortalized B lymphocytes are
able to secrete a 92-kDa metalloproteinase with gelatinolytic activity
which has been purified and identified as being MMP-9. Moreover, the
tissue inhibitor of metalloproteinase was shown to be constitutively
expressed by the B cells. The expression of 92-kDa gelatinase is
mediated by cytokines, growth factors, lipopolysaccharide, concanavalin A, and the tumor promotor phorbol 12-myristate 13-acetate. Time dependence activity increased rapidly up to 24 h of incubation with lipopolysaccharide or concanavalin A stimulation while it requires
a delay and more time to have an optimum effect when cytokines were the
stimulating agents; transforming growth factor-
Human B Lymphocytes Synthesize the 92-kDa Gelatinase, Matrix
Metalloproteinase-9
,
,
,
UPR ES EA 2019,
abolished 92-kDa
gelatinase production. Both staurosporine and wortmannin are inductive
stimuli, and the level of MMP-9 secreted into the media is greater than
that observed with other agents except concanavalin A. Elicitation of
the chemotactic migration of B cells through a model basement membrane
by lipopolysaccharide was shown to be correlated with gelatinase
expression and inhibited by 7 mM captopril. Our study
indicates that Epstein-Barr virus-B lymphocytes express 92-kDa
gelatinase, the production of which can be modified by a variety of
physiological and pharmacological signals which have been shown to
differ according to the cell type.
Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.
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