Individual differences |
Methods | Statistics | Clinical | Educational | Industrial | Professional items | World psychology |
Biological: Behavioural genetics · Evolutionary psychology · Neuroanatomy · Neurochemistry · Neuroendocrinology · Neuroscience · Psychoneuroimmunology · Physiological Psychology · Psychopharmacology (Index, Outline)
|This article needs additional citations for verification.|
Please help improve this article by adding reliable references. Unsourced material may be challenged and removed. (May 2008)
- The title of this article should be CAMP-dependent pathway. The initial letter is capitalized due to technical restrictions.
Mechanism[edit | edit source]
G protein-coupled receptors (GPCRs) are a large family of integral membrane proteins that respond to a variety of extracellular stimuli. Each GPCR binds to and is activated by a specific ligand stimulus that ranges in size from small molecule catecholamines, lipids, or neurotransmitters to large protein hormones. When a GPCR is activated by its extracellular ligand, a conformational change is induced in the receptor that is transmitted to an attached intracellular heterotrimeric G protein complex. The Gs alpha subunit of the stimulated G protein complex exchanges GDP for GTP and is released from the complex.
In a cAMP-dependent pathway, the activated Gs alpha subunit binds to and activates an enzyme called adenylyl cyclase, which, in turn, catalyzes the conversion of ATP into cyclic adenosine monophosphate (cAMP). Increases in concentration of the second messenger cAMP may lead to the activation of
- cyclic nucleotide-gated ion channels
- exchange proteins activated by cAMP (EPAC) such as RAPGEF3
- an enzyme called protein kinase A (PKA).
The PKA enzyme is also known as cAMP-dependent enzyme because it gets activated only if cAMP is present. Once PKA is activated, it phosphorylates a number of other proteins including:
- enzymes that convert glycogen into glucose
- enzymes that promote muscle contraction in the heart leading to an increase in heart rate
- transcription factors, which regulate gene expression
Specificity of signaling between a GPCR and its ultimate molecular target through a cAMP-dependent pathway may be achieved through formation of a multiprotein complex that includes the GPCR, adenylyl cyclase, and the effector protein.
Importance[edit | edit source]
- Main article: function of cAMP-dependent protein kinase
In humans, cAMP works by activating protein kinase A (PKA, cAMP-dependent protein kinase), and, thus, further effects mainly depend on cAMP-dependent protein kinase, which vary based on the type of cell.
cAMP-dependent pathway is necessary for many living organisms and life processes. Many different cell responses are mediated by cAMP. These include increase in heart rate, cortisol secretion, and breakdown of glycogen and fat.
This pathway can activate enzymes and regulate gene expression. The activation of preexisting enzymes is a much faster process, whereas regulation of gene expression is much longer and can take up to hours. The cAMP pathway is studied through loss of function (inhibition) and gain of function (increase) of cAMP.
If cAMP-dependent pathway is not controlled, it can ultimately lead to hyper-proliferation, which may contribute to the development and/or progression of cancer.
Activation[edit | edit source]
Activated GPCRs cause a conformational change in the attached G protein complex, which results in the Gs alpha subunit's exchanging GDP for GTP and separation from the beta and gamma subunits. The Gs alpha subunit, in turn, activates adenylyl cyclase, which quickly converts ATP into cAMP. This leads to the activation of the cAMP-dependent pathway. This pathway can also be activated downstream by directly activating adenylyl cyclase or PKA.
Molecules that activate cAMP pathway include:
- cholera toxin - increase cAMP levels
- forskolin - a diterpene natural product that activates adenylyl cyclase
- caffeine and theophylline inhibit cAMP phosphodiesterase, which leads to an activation of G proteins that result in the activation of the cAMP pathway
- bucladesine (dibutyryl cAMP, db cAMP) - also a phosphodiesterase inhibitor
- pertussis toxin, which increase cAMP levels by inhibiting Gi to its GDP (inactive) form. This leads to an increase in adenylyl cyclase, therefore increasing cAMP levels, which can lead to an increase in insulin and therefore hypoglycemia
Deactivation[edit | edit source]
The Gs alpha subunit slowly catalyzes the hydrolysis of GTP to GDP, which in turn deactivates the Gs protein, shutting off the cAMP pathway. The pathway may also be deactivated downstream by directly inhibiting adenylyl cyclase or dephosphorylating the proteins phosphorylated by PKA.
Molecules that inhibit the cAMP pathway include:
- cAMP phosphodiesterase dephospohorylates cAMP into AMP, reducing the cAMP levels
- Gi protein, which is a G protein that inhibits adenylyl cyclase, reducing cAMP levels.
References[edit | edit source]
- Bruce Alberts, Alexander Johnson, Julian Lewis, Martin Raff, Dennis Bray, Karen Hopkin, Keith Roberts, Peter Walter (2004). Essential cell biology, 2, New York: Garland Science.
- Hanoune J, Defer N (2001). Regulation and role of adenylyl cyclase isoforms. Annu. Rev. Pharmacol. Toxicol. 41: 145–74.
- Kaupp UB, Seifert R (July 2002). Cyclic nucleotide-gated ion channels. Physiol. Rev. 82 (3): 769–824.
- Bos JL (December 2006). Epac proteins: multi-purpose cAMP targets. Trends Biochem. Sci. 31 (12): 680–6.
- Meinkoth JL, Alberts AS, Went W, Fantozzi D, Taylor SS, Hagiwara M, Montminy M, Feramisco JR (November 1993). Signal transduction through the cAMP-dependent protein kinase. Mol. Cell. Biochem. 127-128: 179–86.
- Walsh DA, Van Patten SM (December 1994). Multiple pathway signal transduction by the cAMP-dependent protein kinase. Faseb J. 8 (15): 1227–36.
- Davare MA, Avdonin V, Hall DD, Peden EM, Burette A, Weinberg RJ, Horne MC, Hoshi T, Hell JW (July 2001). A β2 adrenergic receptor signaling complex assembled with the Ca2+ channel Cav1.2. Science 293 (5527): 98–101.
|This page uses Creative Commons Licensed content from Wikipedia (view authors).|