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J. Biol. Chem., Vol. 261, Issue 20, 9246-9249, 07, 1986
R Heumann and H Thoenen
In previous experiments, it has been demonstrated that, in rat irides in
culture, a rapid increase in nerve growth factor (NGF) levels occurred (see
Barth, E.-M., Korsching, S., and Thoenen, H. (1984) J. Cell Biol. 99,
839-843). We have now determined the levels of mRNANGF in rat irides as a
function of time in culture as well. After an initial lag period of 2 h,
mRNANGF levels were transiently increased, so that after 12 h, they had
increased 35-fold with respect to zero time. In contrast, poly(A)+ RNA
levels dropped to 55% of the zero time values within 5 h, recovered to 85%
after 24 h, and remained constant until the end of the observation period.
Total ribosomal RNA was found to remain constant, indicating that there was
no nonspecific decline of overall metabolic function. Actinomycin D
prevented the increase in mRNANGF without reducing the basic mRNANGF levels
over a 5-h time period, indicating that the enhanced synthesis of NGF in
the rat iris in culture is primarily mediated by an augmented production of
mRNANGF. The increases of mRNANGF, cellular NGF, and NGF released into the
medium were found to be strictly sequential. Monensin selectively abolished
the increased production of mature NGF (see Barth et al.) but not of
mRNANGF, suggesting that the processing of NGF precursor is prevented.
Comparison between the time course of changes in nerve growth factor protein levels and those of its messenger RNA in the cultured rat iris
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