Taste receptors of the tongue are present in the taste buds of papillae.
A taste receptor is a type of receptor which facilitates the sensation of taste. When food or other substances enter the mouth, molecules interact with saliva and are bound to taste receptors in the oral cavity and other locations. Molecules which give a sensation of taste are considered "sapid".
Taste receptors are divided into two families:
- Type 1, sweet, first characterized in 2001: TAS1R1 – TAS1R3
- Type 2, bitter, first characterized in 2000: TAS2R1 – TAS2R50, and TAS2R60
Combinations of these receptors in dimers or other complexes contributes to different perceptions of taste.
Visual, olfactive, “sapictive” (the perception of tastes), trigeminal (hot, cool), mechanical, all contribute to the perception of taste. Of these, transient receptor potential cation channel subfamily V member 1 (TRPV1) vanilloid receptors are responsible for the perception of heat from some molecules such as capsaicin, and a CMR1 receptor is responsible for the perception of cold from molecules such as menthol, eucaplyptol, and icilin.
The gustatory system consists of taste receptor cells in taste buds. Taste buds, in turn, are contained in structures called papillae. There are three types of papillae involved in taste: fungiform papillae, foliate papillae, and circumvallate papillae. (The fourth type - filiform papillae do not contain taste buds). Beyond the papillae, taste receptors are also in the palate and early parts of the digestive system like the larynx and upper esophagus. There are three cranial nerves that innervate the tongue; the vagus nerve, glossopharyngeal nerve, and the facial nerve. The glossopharyngeal nerve and the chorda tympani branch of the facial nerve innervate the TAS1R and TAS2R taste receptors.
In 2010, researchers found bitter receptors in lung tissue, which cause airways to relax when a bitter substance is encountered. They believe this mechanism is evolutionarily adaptive because it helps clear lung infections, but could also be exploited to treat asthma and chronic obstructive pulmonary disease.
Taste helps to identify toxins and maintain nutrition. Five basic tastes are recognized today: salty, sweet, bitter, sour, and umami. Salty and sour taste sensations are both detected through ion channels. Sweet, bitter, and umami tastes, however, are detected by way of G protein-coupled taste receptors.
Mechanism of action
The standard bitter, sweet, or umami taste receptor is a G protein-coupled receptor with seven transmembrane domains. Ligand binding at the taste receptors activate second messenger cascades to depolarize the taste cell. Gustducin is the most common taste Gα subunit, having a major role in TAS2R bitter taste reception. Gustducin is a homologue for transducin, a G-protein involved in vision transduction. Additionally, taste receptors share the use of the TRPM5 ion channel, as well as a phospholipase PLCβ2.
The TAS1R1+TAS1R3 heterodimer receptor functions as the umami (savory) receptor, responding to L-amino acid binding, especially L-glutamate. The umami taste is most frequently associated with the food additive monosodium glutamate (MSG) and can be enhanced through the binding of inosine monophosphate (IMP) and guanosine monophosphate (GMP) molecules. TAS1R1+3 expressing cells are found mostly in the fungiform papillae at the tip and edges of the tongue and palate taste receptor cells in the roof of the mouth. These cells are shown to synapse upon the chorda tympani nerves to send their signals to the brain, although some activation of the glossopharyngeal nerve has been found.
The TAS1R2+TAS1R3 heterodimer receptor functions as the sweet receptor by binding to a wide variety of sugars and sugar substitutes. TAS1R2+3 expressing cells are found in circumvallate papillae and foliate papillae near the back of the tongue and palate taste receptor cells in the roof of the mouth. These cells are shown to synapse upon the chorda tympani and glossopharyngeal nerves to send their signals to the brain. The TAS1R3 homodimer also functions as a sweet receptor in much the same way as TAS1R2+3 but has decreased sensitivity to sweet substances. Natural sugars are more easily detected by the TAS1R3 receptor than sugar substitutes. This may help explain why sugar and artificial sweeteners have different tastes.
The TAS2R proteins function as bitter taste receptors. There are 43 human TAS2R genes, each of which (excluding the five pseudogenes) lacks introns and codes for a GPCR protein. These proteins, as opposed to TAS1R proteins, have short extracellular domains and are located in circumvallate papillae, palate, foliate papillae, and epiglottis taste buds, with reduced expression in fungiform papillae. Though it is certain that multiple TAS2Rs are expressed in one taste receptor cell, it is still debated whether mammals can distinguish between the tastes of different bitter ligands. Some overlap must occur, however, as there are far more bitter compounds than there are TAS2R genes. Common bitter ligands include cycloheximide, denatonium, PROP (6-n-propyl-2-thiouracil), PTC (phenylthiocarbamide), and β-glucopyranosides.
Signal transduction of bitter stimuli is accomplished via the α-subunit of gustducin. This G protein subunit activates a taste phosphodiesterase and decreases cyclic nucleotide levels. Further steps in the transduction pathway are still unknown. The βγ-subunit of gustducin also mediates taste by activating IP3 (inositol triphosphate) and DAG (diglyceride). These second messengers may open gated ion channels or may cause release of internal calcium. Though all TAS2Rs are located in gustducin-containing cells, knockout of gustducin does not completely abolish sensitivity to bitter compounds, suggesting a redundant mechanism for bitter tasting (unsurprising given that a bitter taste generally signals the presence of a toxin). One proposed mechanism for gustducin-independent bitter tasting is via ion channel interaction by specific bitter ligands, similar to the ion channel interaction which occurs in the tasting of sour and salty stimuli.
One of the best-researched TAS2R proteins is TAS2R38, which contributes to the tasting of both PROP and PTC. It is also the only taste receptor whose polymorphisms are shown to be responsible for differences in taste perception. Current studies are focused on determining other such taste phenotype-determining polymorphisms.
While sour taste has historically been regarded as the domain of ion channels, receptors for sour taste are now being proposed. HCN1 and HCN4 (HCN channels) were two such proposals; both of these receptors are cyclic nucleotide-gated channels. The two ion channels suggested to contribute to sour taste are ACCN1 and TASK-1.
Various receptors have also been proposed for salty tastes, along with the possible taste detection of lipids, complex carbohydrates, and water. Evidence for these receptors is, however, shaky at best, and is often unconvincing in mammal studies. For example, the proposed ENaC receptor for sodium detection can only be shown to contribute to sodium taste in Drosophilia.
An enzyme connected to the sour receptor transmits information about carbonated water.
A possible taste receptor for fat, CD36, has been identified.  CD36 has been localized to the circumvallate and foliate papillae, which are present in taste buds, and research has shown that the CD36 receptor binds long chain fatty acids. Differences in the amount of CD36 expression in human subjects was associated with their ability to taste fats, creating a case for the receptor's relationship to fat tasting. Further research into the CD36 receptor could be useful in determining the existence of a true fat-tasting receptor.
Human bitter taste receptor genes are named TAS2R1 to TAS2R64, with many gaps due to non-existent genes, pseudogenes or proposed genes that have not been annotated to the most recent human genome assembly. Many bitter taste receptor genes also have confusing synonym names with several different gene names referring to the same gene. See table below for full list of human bitter taste receptor genes:
|TAS2R6||7||not annotated in human genome assembly|
|TAS2R11||absent in humans|
|TAS2R17||absent in humans|
|TAS2R21||absent in humans|
|TAS2R22||12||not annotated in human genome assembly|
|TAS2R24||absent in humans|
|TAS2R25||absent in humans|
|TAS2R27||absent in humans|
|TAS2R28||absent in humans|
|TAS2R29||absent in humans|
|TAS2R32||absent in humans|
|TAS2R33||12||not annotated in human genome assembly|
|TAS2R34||absent in humans|
|TAS2R35||absent in humans|
|TAS2R36||12||not annotated in human genome assembly|
|TAS2R37||12||not annotated in human genome assembly|
|TAS2R52||absent in humans|
|TAS2R53||absent in humans|
|TAS2R54||absent in humans|
|TAS2R55||absent in humans|
|TAS2R56||absent in humans|
|TAS2R57||absent in humans|
|TAS2R58||absent in humans|
|TAS2R59||absent in humans|
- This, Hervé (2012). "The Science of the Oven - Excerpt from Chapter 1". Retrieved 30 Apr 2014.
- Nelson G, Hoon MA, Chandrashekar J, Zhang Y, Ryba NJ, Zuker CS (August 2001). "Mammalian sweet taste receptors". Cell 106 (3): 381–90. doi:10.1016/S0092-8674(01)00451-2. PMID 11509186.
- Adler E, Hoon MA, Mueller KL, Chandrashekar J, Ryba NJ, Zuker CS (March 2000). "A novel family of mammalian taste receptors". Cell 100 (6): 693–702. doi:10.1016/S0092-8674(00)80705-9. PMID 10761934.
- Bachmanov, AA.; Beauchamp, GK. (2007). "Taste receptor genes.". Annu Rev Nutr 27: 389–414. doi:10.1146/annurev.nutr.26.061505.111329. PMC 2721271. PMID 17444812.
- Sainz E, Cavenagh MM, LopezJimenez ND, Gutierrez JC, Battey JF, Northup JK, Sullivan SL (2007). "The G-protein coupling properties of the human sweet and amino acid taste receptors". Developmental Neurobiology 67 (7): 948–959. doi:10.1002/dneu.20403. PMID 17506496.
- Zhang Y, Hoon MA, Chandrashekar J, Mueller KL, Cook B, Wu D, Zuker CS, Ryba NJ (2003). "Coding of sweet, bitter, and umami tastes: Different receptor cells sharing similar signaling pathways". Cell 112 (3): 293–301. doi:10.1016/S0092-8674(03)00071-0. PMID 12581520.
- Nelson g, H. M. (2001). "Mammalian sweet taste receptors". Cell 106 (3): 381–390. doi:10.1016/S0092-8674(01)00451-2. PMID 11509186.
- Nelson g, C. J.; Chandrashekar, J.; Hoon, M. A.; Feng, L.; Zhao, G.; Ryba, N. J. P.; Zuker, C. S. (2002). "An amino-acid taste receptor". Nature 416 (6877): 199–202. doi:10.1038/nature726. PMID 11894099.
- Delay Er, B. A.; Beaver, A. J.; Wagner, K. A.; Stapleton, J. R.; Harbaugh, J. O.; Catron, K. D.; Roper, S. D. (2000). "Taste preference synergy between glutamate receptor agonists and inosine monophosphate in rats". Chemical senses 25 (5): 507–515. doi:10.1093/chemse/25.5.507. PMID 11015322.
- Danilova v, H. G. (2003). "Comparison of the responses of the chorda tympani and glossopharyngeal nerves to taste stimuli in C57BL/6J mice". BMC neuroscience 4: 5–6. doi:10.1186/1471-2202-4-5. PMC 153500. PMID 12617752.
- Li x, S. L. (2002). "Human receptors for sweet and umami taste". Proceedings of the National Academy of Sciences 99 (7): 4692–4696. doi:10.1073/pnas.072090199. PMC 123709. PMID 11917125.
- Zhao Gq, Z. Y.; Zhang, Y.; Hoon, M. A.; Chandrashekar, J.; Erlenbach, I.; Ryba, N. J. P.; Zuker, C. S. (2003). "The receptors for mammalian sweet and umami taste". Cell 115 (3): 255–266. doi:10.1016/S0092-8674(03)00844-4. PMID 14636554.
- Chandrashekar j, M. K.; Mueller, K. L.; Hoon, M. A.; Adler, E.; Feng, L.; Guo, W.; Zuker, C. S.; Ryba, N. J. (2000). "T2Rs function as bitter taste receptors". Cell 100 (6): 703–711. doi:10.1016/S0092-8674(00)80706-0. PMID 10761935.
- Margolskee RF (2001). "Molecular Mechanisms of Bitter and Sweet Taste Transduction". Journal of Biological Chemistry 277 (1): 1–4. doi:10.1074/jbc.R100054200. PMID 11696554.
- Adler E Hoon MA, Mueller KL, Chandrashekar J, Ryba JP, Zucker CS, Patton A (2000). "A Novel Family of Mammalian Taste Receptors - An Investigative Review". Davidson College Biology Department. Retrieved 2008-08-11.
- taste receptors, type 1 at the US National Library of Medicine Medical Subject Headings (MeSH)
- taste receptors, type 2 at the US National Library of Medicine Medical Subject Headings (MeSH)