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Volume 270,
Number 50,
Issue of December 15, 1995 pp. 29656-29659
©1995 by The American Society for Biochemistry and Molecular Biology, Inc.
Release of
Gelatinase A (Matrix Metalloproteinase 2) Induced by Photolysis of
Caged Phosphatidic Acid in HT 1080 Metastatic Fibrosarcoma Cells
(Received for publication, October
16, 1995)
Ben-Tsion
Williger
,
Reuven
Reich
,
Michal
Neeman
,
Tuvia
Bercovici
,
Mordechai
Liscovitch
Phosphatidic acid (PA) is a putative novel messenger in signal
transduction and membrane traffic. We have synthesized a photolyzable
derivative of PA, termed caged PA (cPA), which may be utilized as a new
tool in studies of PA-mediated cellular events.
1-(2-Nitrophenyl)diazoethane, synthesized from 2-nitroacetophenone, was
reacted with dipalmitoyl-PA to yield a 1-(2-nitrophenyl)ethyl ester of
PA. Photolysis of the compound by ultraviolet light resulted in the
formation of phosphatidic acid. The structure of the compound and of
its photolytic products was verified by NMR spectroscopy. The utility
of cPA was examined in HT 1080 metastatic fibrosarcoma cells, in which
the formation of PA by phospholipase D was implicated in
laminin-induced release of gelatinase A (matrix metalloproteinase 2
(MMP-2)). The uptake of cPA by HT 1080 cells reached a plateau after
120 min of incubation. Ultraviolet illumination of cPA-loaded cells for
5 s resulted in photolysis of 1.8% of the cell-incorporated cPA. The
photolysis of cPA caused a 2-fold elevation in the release of MMP-2 to
the medium, whereas nonphotolyzed cPA caused no change in MMP-2
release. Moreover, the effect of cPA photolysis was significantly
higher than that obtained with extracellularly introduced PA. Thus, the
effect of laminin on MMP-2 secretion can be mimicked by photolysis of
cPA, suggesting a pivotal role for phospholipase D in laminin-induced
cancer cell invasiveness and metastasis. These results indicate that
cPA could serve as a unique tool for studying the cellular roles of PA.

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Copyright © 1995 by the American Society for Biochemistry and Molecular Biology.
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