The effect of dexamethasone on the expression of proteolipid protein (PLP) and myelin-associated glycoprotein (MAG) genes was investigated in rat C6 glioma cells. The steady state level of the respective mRNAs was quantitated by Northern blot analysis. The treatment of cells with dexamethasone trans
Cyclic AMP-induced upregulation of proteolipid protein and myelin associated glycoprotein gene expression in C6 cells
✍ Scribed by P. Ye; M. Kanoh; W. Zhu; I. Laszkiewicz; J. E. Royland; R. C. Wiggins; Dr. G. Konat
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 625 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0360-4012
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✦ Synopsis
Abstract
A Model culture system of C6 rat glioma cells was used to test the involvement of cAMP in the regulation of the myelin PLP and MAG genes. The treatment of cells with isoproterenol (10^−5^to 10^−8^M) upregulated the expression of the PLP and MAG genes in a concentration‐dependent manner. The mRNAf or PLP reached a maximum (sevenfold higher than in control cells) after about 12–24 hr, then declined to approximately fourfold over the control level. The response of MAG gene was delayed by at least 36 hr, and the level of MAG mRNA reached a maximum of approximately 48‐fold over the control level on the fourth day in culture. The co‐administration of propranolol blocked the effect of isoproterenol, whereas 10^−5^M forskolin simulated the effect of isoproterenol, inducating a role of camp in the signal transduction cascades leading to upregulation of the myelin genes. However, the dissimilarity in the timing and the extent of upregulation of the PLP and MAG genes by cAMP‐stimulating agents indicate the existence of different intracellular mechanisms for the activation of these two genes. Cyclocheximide blocked the stimulatory effect of isopoterenol on both the PLP and MAG genes, indicating that the effect of cAMP on the myelin genes is mediated by protein product(s) of other cAMP response gene(s).
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