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, eucalyptol, 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.
Savory or Glutamates
The TAS1R1+TAS1R3 heterodimer receptor functions as the 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 (Aug 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 (Mar 2000). "A novel family of mammalian taste receptors". Cell 100 (6): 693–702. doi:10.1016/S0092-8674(00)80705-9. PMID 10761934.
- Deshpande DA, Wang WC, McIlmoyle EL, Robinett KS, Schillinger RM, An SS, Sham JS, Liggett SB (Nov 2010). "Bitter taste receptors on airway smooth muscle bronchodilate by localized calcium signaling and reverse obstruction". Nature Medicine 16 (11): 1299–304. doi:10.1038/nm.2237. PMC 3066567. PMID 20972434.
- Bachmanov AA, Beauchamp GK (2007). "Taste receptor genes". Annual Review of Nutrition 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 (Jun 2007). "The G-protein coupling properties of the human sweet and amino acid taste receptors". Developmental Neurobiology 67 (7): 948–59. doi:10.1002/dneu.20403. PMID 17506496.
- Zhang Y, Hoon MA, Chandrashekar J, Mueller KL, Cook B, Wu D, Zuker CS, Ryba NJ (Feb 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, Chandrashekar J, Hoon MA, Feng L, Zhao G, Ryba NJ, Zuker CS (Mar 2002). "An amino-acid taste receptor". Nature 416 (6877): 199–202. doi:10.1038/nature726. PMID 11894099.
- Delay ER, Beaver AJ, Wagner KA, Stapleton JR, Harbaugh JO, Catron KD, Roper SD (Oct 2000). "Taste preference synergy between glutamate receptor agonists and inosine monophosphate in rats". Chemical Senses 25 (5): 507–15. doi:10.1093/chemse/25.5.507. PMID 11015322.
- Danilova V, Hellekant G (Mar 2003). "Comparison of the responses of the chorda tympani and glossopharyngeal nerves to taste stimuli in C57BL/6J mice". BMC Neuroscience 4: 5. doi:10.1186/1471-2202-4-5. PMC 153500. PMID 12617752.
- Li X, Staszewski L, Xu H, Durick K, Zoller M, Adler E (Apr 2002). "Human receptors for sweet and umami taste". Proceedings of the National Academy of Sciences of the United States of America 99 (7): 4692–6. doi:10.1073/pnas.072090199. PMC 123709. PMID 11917125.
- Zhao GQ, Zhang Y, Hoon MA, Chandrashekar J, Erlenbach I, Ryba NJ, Zuker CS (Oct 2003). "The receptors for mammalian sweet and umami taste". Cell 115 (3): 255–66. doi:10.1016/S0092-8674(03)00844-4. PMID 14636554.
- Chandrashekar J, Mueller KL, Hoon MA, Adler E, Feng L, Guo W, Zuker CS, Ryba NJ (Mar 2000). "T2Rs function as bitter taste receptors". Cell 100 (6): 703–11. doi:10.1016/S0092-8674(00)80706-0. PMID 10761935.
- Margolskee RF (Jan 2002). "Molecular mechanisms of bitter and sweet taste transduction". The Journal of Biological Chemistry 277 (1): 1–4. doi:10.1074/jbc.R100054200. PMID 11696554.
- Laugerette F, Passilly-Degrace P, Patris B, Niot I, Febbraio M, Montmayeur JP, Besnard P (Nov 2005). "CD36 involvement in orosensory detection of dietary lipids, spontaneous fat preference, and digestive secretions". The Journal of Clinical Investigation 115 (11): 3177–84. doi:10.1172/JCI25299. PMC 1265871. PMID 16276419.
- Simons PJ, Kummer JA, Luiken JJ, Boon L (Dec 2011). "Apical CD36 immunolocalization in human and porcine taste buds from circumvallate and foliate papillae". Acta Histochemica 113 (8): 839–43. doi:10.1016/j.acthis.2010.08.006. PMID 20950842.
- Baillie AG, Coburn CT, Abumrad NA (Sep 1996). "Reversible binding of long-chain fatty acids to purified FAT, the adipose CD36 homolog". The Journal of Membrane Biology 153 (1): 75–81. doi:10.1007/s002329900111. PMID 8694909.
- Pepino MY, Love-Gregory L, Klein S, Abumrad NA (Mar 2012). "The fatty acid translocase gene CD36 and lingual lipase influence oral sensitivity to fat in obese subjects". Journal of Lipid Research 53 (3): 561–6. doi:10.1194/jlr.M021873. PMC 3276480. PMID 22210925.
- DiPatrizio NV (Sep 2014). "Is fat taste ready for primetime?". Physiology & Behavior 136: 145–54. doi:10.1016/j.physbeh.2014.03.002. PMID 24631296.
- Cartoni C, Yasumatsu K, Ohkuri T, Shigemura N, Yoshida R, Godinot N, le Coutre J, Ninomiya Y, Damak S (Jun 2010). "Taste preference for fatty acids is mediated by GPR40 and GPR120". The Journal of Neuroscience 30 (25): 8376–82. doi:10.1523/JNEUROSCI.0496-10.2010. PMID 20573884.
- Mattes RD (Sep 2011). "Accumulating evidence supports a taste component for free fatty acids in humans". Physiology & Behavior 104 (4): 624–31. doi:10.1016/j.physbeh.2011.05.002. PMC 3139746. PMID 21557960.
- Liu P, Shah BP, Croasdell S, Gilbertson TA (Jun 2011). "Transient receptor potential channel type M5 is essential for fat taste". The Journal of Neuroscience 31 (23): 8634–42. doi:10.1523/JNEUROSCI.6273-10.2011. PMC 3125678. PMID 21653867.
- 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)