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Volume 270,
Number 35,
Issue of September 01, pp. 20560-20567, 1995
©1995 by The American Society for Biochemistry and Molecular Biology, Inc.
Activation of
Cell Growth Inhibitor by Ectoprotein Kinase-mediated Phosphorylation in
Transformed Mouse Fibroblasts
(Received for publication, March 17, 1995)
Ilan
Friedberg
, <WBR>
Ilana
Belzer
, <WBR>
Orly
Oged-Plesz
, <WBR>
Dieter
Kuebler
Our previous studies have shown that exogenous ATP induces cell
growth inhibition in transformed mouse fibroblasts, 3T6 cells, whereas
the growth of their nontransformed counterparts, Swiss 3T3 cells, is
only slightly affected. In this study a similar selective, ATP-induced
growth inhibition was found in Balb/c SV40-3T3 cells and in
primary cultures of adenovirus-transformed murine fibroblasts. The
inhibitory activity was found in the conditioned media of ATP-treated
cultures. Several lines of evidence have shown that ectoprotein kinase
(ecto-PK) plays a major role in the ATP-induced growth inhibition. (a) There is a good correlation between the activity of
ecto-PK and the ability of ATP to induce cell growth inhibition. (b) The removal of the ecto-PK from the cell surface prevents
the ATP-induced growth inhibition. (c) Addition of the removed
enzyme to the cell culture reconstitutes the ability of ATP to induced
growth inhibition. (d) Serum-containing, or serum-free,
conditioned media from untreated cultures gain an inhibitory activity
after their phosphorylation, and dephosphorylation of conditioned media
from ATP-treated cultures results in the loss of the inhibitory
activity. (e) Growth medium by itself does not inhibit cell
proliferation after its phosphorylation. The findings described in d and e indicate, as well, that the ATP-induced
growth inhibitor is produced by the cells. The putative inhibitor was
found to be a protein, with an apparent molecular mass of 13 kDa. The
selectivity of the inhibition for transformed cells is due to the
higher level of ecto-PK in these cells, as well as to their higher
susceptibility to the inhibitor, as compared with their nontransformed
counterparts.

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