Global InformationSecond messenger system information
Second messengers are intracellular signaling molecules released by the cell in response to exposure to extracellular signaling molecules—the first messengers. (Intercellular signals, a non-local form of cell signaling, encompassing both first messengers and second messengers, are classified as autocrine, juxtacrine, paracrine, and endocrine depending on the range of the signal.) Second messengers trigger physiological changes at cellular level such as proliferation, differentiation, migration, survival, apoptosis and depolarization.
They are one of the triggers of intracellular signal transduction cascades.[1]
Examples of second messenger molecules include cyclic AMP, cyclic GMP, inositol triphosphate, diacylglycerol, and calcium.[2] First messengers are extracellular factors, often hormones or neurotransmitters, such as epinephrine, growth hormone, and serotonin. Because peptide hormones and neurotransmitters typically are biochemically hydrophilic molecules, these first messengers may not physically cross the phospholipid bilayer to initiate changes within the cell directly—unlike steroid hormones, which usually do. This functional limitation requires the cell to have signal transduction mechanisms to transduce first messenger into second messengers, so that the extracellular signal may be propagated intracellularly. An important feature of the second messenger signaling 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.[3][4] For example, RasGTP signals link with the mitogen activated protein kinase (MAPK) cascade to amplify the allosteric activation of proliferative transcription factors such as 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.[5] The mechanisms were worked out in detail by Martin Rodbell and Alfred G. Gilman, who won the 1994 Nobel Prize.[6][7]
Secondary messenger systems can be synthesized and activated by enzymes, for example, the cyclases that synthesize cyclic nucleotides, or by opening of ion channels to allow influx of metal ions, for example Ca2+ signaling. These small molecules bind and activate protein kinases, ion channels, and other proteins, thus continuing the signaling cascade.
- ^ Kodis EJ, Smindak RJ, Kefauver JM, Heffner DL, Aschenbach KL, Brennan ER, Chan K, Gamage KK, Lambeth PS, Lawler JR, Sikora AK (May 2001). "First Messengers". eLS. Chichester: John Wiley & Sons Ltd. doi:10.1002/9780470015902.a0024167. ISBN 978-0470016176.
- ^ Pollard TD, Earnshaw WC, Lippincott-Schwartz J, Johnson G, eds. (2017-01-01). "Second Messengers". Cell Biology (3rd ed.). Elsevier Inc. pp. 443–462. doi:10.1016/B978-0-323-34126-4.00026-8. ISBN 978-0-323-34126-4.
- ^ Second+Messenger+Systems at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
- ^ "Second Messengers". www.biology-pages.info. Retrieved 2018-12-03.
- ^ Reece J, Campbell N (2002). Biology. San Francisco: Benjamin Cummings. ISBN 978-0-8053-6624-2.
- ^ "The Nobel Prize in Physiology or Medicine 1994". NobelPrize.org. Retrieved 2018-12-03.
- ^ "The Nobel Prize in Physiology or Medicine 1994". NobelPrize.org. Retrieved 2018-12-03.