Exp Mol Med.
2000 Dec;32(4):235-242.
Multi-facet expressions of adenylate cyclase isoforms in B16-F10 melanoma cells differentiated by forskolin treatment
- Affiliations
-
- 1Department of Biochemistry and Cancer Research Institute, Seoul National University College of Medicine, Korea.
Abstract
- The terminal differentiation of malignant melanoma cells is known to be induced
by activating cAMP signaling pathway with alpha-MSH or cAMP analogues. However,
sustained activation of cAMP signaling system that induces the differentiation
of melanoma cells, also induces the desensitization of the pathway at the
receptor level. Nevertheless, the adaptation of adenylate cyclase (AC)
expression by sustained activation of cAMP signaling system has not been clearly
understood. This study was performed to examine whether the sustained activation
of cAMP system induce changes in the expression AC isoforms as an adaptation
mechanism. Treatment of B16/F10 murine melanoma cells with 100 mM forskolin for
6 days resulted in differentiation, melanin accumulation and increased
expression of tyrosine hydroxylase mRNA. In the forskolin-treated melanoma
cells, change in expression of various AC isoform at the transcription level was
detected by reverse-transcription polymerase chain reaction (RT-PCR). Expression
of AC isoform mRNA: ACI, III, VI, VII, and IX increased to the level of 196-392%
of the control whereas the level of ACII was decreased by 30%. The cAMP
concentration was increased both in basal and alpha-MSH stimulated cells, but
the AC activity was decreased in the forskolin treated cells. Thus, these
results suggest that sustained activation of cAMP system induces differential
expression of AC isoforms, which results in increase of cAMP accumulation.