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(Received for publication, October 17,
1995; and in revised form, January 8, 1996)
Volume 271,
Number 16,
Issue of April 19, 1996 pp. 9223-9230
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
-Thymosins
Are Not Simple Actin Monomer Buffering Proteins
INSIGHTS FROM OVEREXPRESSION STUDIES
-Thymosins are the currently favored candidates for
maintaining the large actin monomer (G-actin) pool in living cells. To
determine if
-thymosin behaves like a simple G-actin buffering
agent in the complex environment of a cell, we overexpressed thymosin
10 (T
10) in NIH3T3 cells and determined the effect on the
monomer/polymer equilibrium. T
10 is the predominant
-thymosin
isoform in the NIH3T3 cell line, and it is present in approximately
equal molar ratio to profilin and cofilin/actin depolymerizing factor,
two other well characterized actin monomer binding proteins. Clonal
cell lines that overexpressed three times more T
10 had
23-33% more polymerized actin than control cells, and the
filaments appeared thicker after staining with fluorescent phalloidin.
There was no change in total actin, profilin, and cofilin/actin
depolymerizing factor content. The overexpressing cells were more
motile; they spread faster and had higher chemotactic and wound healing
activity. Assuming that there is no compensatory inactivation of the
other classes of monomer binding proteins, our paradoxical observation
can be accounted for quantitatively by a parallel in vitro study (Carlier, M.-F., Didry, D., Erk, I., Lepault, J., Van Troys,
L., Vanderkekove, J., Perelroizen, I., Yin, H. L., Doi, Y., and
Pantaloni, D.,(1996) J. Biol. Chem. 271, 9231-9239).
-Thymosin at levels comparable with that found in the
overexpressing cells binds actin filaments and decreases the critical
concentration (C
) for actin polymerization. This
reduces the monomer buffering ability of
-thymosin, so that above
a certain threshold an incremental increase in thymosin does not lead
to a corresponding increase in G-actin. Furthermore, the decrease in C
reduces the buffering capacity of the other
actin monomer binding proteins. As a consequence, an increase in
-thymosin does not necessarily result in a proportionate increase
in actin monomer content in a complex environment containing other
actin monomer binding proteins. The outcome depends on the level of
-thymosin expression relative to the composition of the other
actin monomer binding protien. Our results suggest that
-thymosins
are not simple actin buffering proteins and that their biphasic action
may have physiological significance.
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