Prothymosin alpha (PTA) mRNA and histone H4 (H4) mRNA levels were stud
ied in various experimental conditions that affected GH1 pituitary tum
or cell proliferation. Cell proliferation and progression through the
cell cycle was assessed by counting cells, H-3-thymidine incorporation
and flow cytometry. PTA mRNA levels were decreased in a time-dependen
t fashion following serum deprivation; when the cells were induced to
grow by serum refeeding, PTA mRNA expression was greatly stimulated. I
nterestingly, after caprylic acid treatment (2.5 mM for 24 h) that arr
ested cells in the G0/G1 phase of the cell cycle, PTA mRNA and H4 mRNA
levels were almost undetectable; conversely, following caprylic acid
withdrawal, PTA mRNA and H4 mRNA expression were greatly stimulated. F
urthermore, cells cultured in T3-deprived serum, which was found to de
crease GH1 cell proliferation, had low levels of PTA and H4 mRNAs. Thi
s effect was reversed by the addition of nanomolar concentrations of T
3 to the culture. On the other hand, IGF-1 addition to the culture did
not substantially modify PTA mRNA levels. The present data clearly in
dicate that PTA mRNA expression is tied to the proliferating activity
of GH1 cells and, thus, could be used as a marker of the action that v
arious agents have on GH1 cell proliferation.