Second messenger system
Second messengers are intracellular signalling molecules released by the cell to trigger physiological changes such as proliferation, differentiation, migration, survival, and apoptosis. Secondary messengers are therefore one of the initiating components of intracellular signal transduction cascades. Examples of second messenger molecules include Cyclic AMP, Cyclic GMP, Inositol Triphosphate, Diacylglycerol, and Calcium. The cell releases second messenger molecules in response to exposure to extracellular signals - the First messengers. First Messengers are extracellular substances that include peptide hormones such as epinephrine, growth factors, and neurotransmitters such as serotonin. Because hormones and neurotransmitters typically comprise biochemically hydrophilic molecules, first messengers may not physically cross the phospholipid bilayer cell membrane to initiate changes within the cell directly. This functional limitation necessitates the cell to devise signal transduction mechanisms to transduce first into second messengers, so that the extracellular signal may be propagated intracellularly. An important feature of the second messenger signalling system is that second messengers may be coupled downstream to multi-cyclic kinase cascades to greatly amplify the strength of the original first messenger signal. For example, Ras.GTP signals link with the Mitogen Activated Protein Kinase (MAPK) cascade to amplify the allosteric activation of proliferative transcription factors like Myc and CREB.
Earl Wilbur Sutherland, Jr., discovered second messengers, for which he won the 1971 Nobel Prize in Physiology or Medicine. Sutherland saw that epinephrine would stimulate the liver to convert glycogen to glucose (sugar) in liver cells, but epinephrine alone would not convert glycogen to glucose. He found that epinephrine had to trigger a second messenger, cyclic AMP, for the liver to convert glycogen to glucose. The mechanisms were worked out in detail by Martin Rodbell and Alfred G. Gilman, who won the 1994 Nobel prize.
Secondary messenger systems can be synthesized and activated by enzymes, like the cyclases that synthesize cyclic nucleotides, or by opening of ion channels to allow influx of metal ions, like Ca2+ signaling. These small molecules bind and activate protein kinases, ion channels, and other proteins, thus continuing the signaling cascade.
Types of secondary messenger molecules
There are three basic types of secondary messenger molecules:
- Hydrophobic molecules: water-insoluble molecules, like diacylglycerol, and phosphatidylinositols, which are membrane-associated and diffuse from the plasma membrane into the intermembrane space where they can reach and regulate membrane-associated effector proteins
- Hydrophilic molecules: water-soluble molecules, like cAMP, cGMP, IP3, and Ca2+, that are located within the cytosol
- Gases: nitric oxide (NO), carbon monoxide (CO) and hydrogen sulphide (H2S) which can diffuse both through cytosol and across cellular membranes.
These intracellular messengers have some properties in common:
- They can be synthesized/released and broken down again in specific reactions by enzymes or ion channels.
- Some (like Ca2+) can be stored in special organelles and quickly released when needed.
- Their production/release and destruction can be localized, enabling the cell to limit space and time of signal activity.
Common mechanisms of secondary messenger systems
There are several different secondary messenger systems (cAMP system, phosphoinositol system, and arachidonic acid system), but they all are quite similar in overall mechanism, though the substances involved in those mechanisms and effects are different.
In all of these cases, a neurotransmitter binds to a membrane-spanning receptor protein molecule. The binding of the neurotransmitter to the receptor changes the receptor and causes it to expose a binding site for a G-protein. The G-protein (named for the GDP and GTP molecules that bind to it) is bound to the inner membrane of the cell and consists of three subunits: alpha, beta and gamma. The G-protein is known as the "transducer."
When the G-protein binds with the receptor, it becomes able to exchange a GDP (guanosine diphosphate) molecule on its alpha subunit for a GTP (guanosine triphosphate) molecule. Once this exchange takes place, the alpha subunit of the G-protein transducer breaks free from the beta and gamma subunits, all parts remaining membrane-bound. The alpha subunit, now free to move along the inner membrane, eventually contacts another membrane-bound protein - the "primary effector."
The primary effector then has an action, which creates a signal that can diffuse within the cell. This signal is called the "secondary messenger." (The neurotransmitter is the first messenger.) The secondary messenger may then activate a "secondary effector" whose effects depend on the particular secondary messenger system.
Calcium ions are responsible for many important physiological functions, such as in muscle contraction, fertilization, and neurotransmitter release. It is normally bound to intracellular components, even though a secondary messenger is a plasma membrane receptor. Calcium regulates the protein calmodulin, and, when bound to calmodulin, it produces an alpha helical structure. This is also important in muscle contraction. The enzyme phospholipase C produces diacylglycerol and inositol trisphosphate, which increases calcium ion permeability into the membrane. Active G-protein open up calcium channels to let calcium ions enter the plasma membrane. The other product of phospholipase C, diacylglycerol, activates protein kinase C, which assists in the activation of cAMP (another second messenger).
|cAMP System||Phosphoinositol system||Arachidonic acid system||cGMP System||Tyrosine kinase system|
|Epinephrine (α2, β1, β2)
Acetylcholine (M1, M3)
|Histamine (Histamine receptor)||-||-|
|ACTH, ANP, CRH, CT, FSH, Glucagon, hCG, LH, MSH, PTH, TSH||AGT, GnRH, GHRH, Oxytocin, TRH||-||ANP, Nitric oxide||INS, IGF, PDGF|
|Signal Transducer||GPCR/Gs (β1, β2), Gi (α2, M2)||GPCR/Gq||Unknown G-protein||-||RTK|
|Primary effector||Adenylyl cyclase||Phospholipase C||Phospholipase A[disambiguation needed]||guanylate cyclase||RasGEF (Grb2-Sos)|
|Second messenger||cAMP (cyclic adenosine monophosphate)||IP3; DAG; Ca2+||Arachidonic acid||cGMP||Ras.GTP (Small G Protein)|
|Secondary effector||protein kinase A||PKC; CaM||5-Lipoxygenase, 12-Lipoxygenase, cycloxygenase||protein kinase G||MAP3K (c-Raf)|
- Kimball, J. "Second messengers".
- Second Messenger Systems at the US National Library of Medicine Medical Subject Headings (MeSH)
- Reece, Jane; Campbell, Neil (2002). Biology. San Francisco: Benjamin Cummings. ISBN 0-8053-6624-5.
- The Discovery of G Proteins
- Signal Transduction in Cells, Nobelprize.org
- Kimball, J. "Second messengers". Retrieved February 10, 2006.