Abstract
Cyclic AMP (cAMP) plays a pivotal role in controlling cell functioning mediating the action of a number of hormones (Sutherland, 1972; Dumont et al, 1989). In such systems binding of a hormone to its receptor stimulates adenylate cyclase to increase synthesis of cAMP. Cyclic AMP then elicits the appropriate cellular response via activation of cAMP-dependent protein kinase (Scott, 1991). Alternatively it may be extruded from the cell (reviewed by Barber and Butcher, 1983 and Brunton and Heasley, 1988) or inactivated. The sole means of its inactivation is through the action of cAMP phosphodiesterases (PDEs) which hydrolyse cAMP to 5′AMP (Beavo, 1990; Houslay and Kilgour, 1990; Conti and Swinnen, 1990). Therefore, cAMP phosphodiesterases play a key role in cAMP metabolism and hence the associated signalling systems.
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Pooley, L., Houslay, M.D. (1995). A Novel Form of Type-IVA cAMP Phosphodiesterase found in rat brain. In: Packer, L., Wirtz, K.W.A. (eds) Signalling Mechanisms — from Transcription Factors to Oxidative Stress. NATO ASI Series, vol 92. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-79675-3_7
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DOI: https://doi.org/10.1007/978-3-642-79675-3_7
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