Chemical Senses Vol. 30 No. suppl 1 © Oxford University
Press 2005; all rights reserved
Mouse Taste Buds Release Serotonin in Response to Taste Stimuli
University of Miami School of Medicine, Miami, FL 33136, USA
Correspondence to be sent to: Stephen D. Roper, e-mail: roper{at}miami.edu
Key words: biosensors, Ca2+ imaging, neurotransmitters, synapses, phospholipase C
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Introduction |
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 Top Introduction Identifying stimulus-evoked...Ca2+-dependence of serotonin...Summary and conclusionsAcknowledgementsReferences |
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Cell-to-cell interactions and synaptic integration may occur within taste buds prior to signals being exported from these peripheral sensory organs to the CNS (Roper, 1992
;
Kaya et al., 2004). In
principle, these interactions could include chemical and electrical synapses between
taste cells and synapses from taste cells to sensory afferent fibers. Knowing which
transmitters are released at synapses in taste buds would help clarify how signals are
processed in taste buds but to date this information is lacking.
A number of neurotransmitter candidates have been proposed for taste bud synapses,
including serotonin (5 hydroxytryptamine, 5HT), glutamate, acetylcholine, ATP, peptides
and others, but none has been unambiguously identified (reviewed by
Nagai et al., 1996). On
balance, the preponderance of evidence suggests that 5HT is one of the transmitters. For
example, 5HT is found in a subset of taste cells in a wide variety of species (Kim and Roper, 1995). Taste bud cells that
possess synapses with nerve fibers take up the 5HT precursor (Takeda, 1977;
Yee et al., 2001), and
tryptophan hydroxylase, the enzyme that converts tryptophan to 5 hydroxytryptophan
(5HTP), is found in taste buds (Cao et
al., 2004). There is indirect evidence from autoradiographic studies
that amphibian taste cells release 5HT when they are depolarized (Nagai et al., 1998). Pharmacological and molecular
biological studies suggest that taste cells express 5HT1A-like receptors and
primary afferent fibers possess 5HT3 receptors (Delay et al., 1997;
Herness and Chen, 1997;
Kaya et al., 2004). Yet
despite all the above evidence, one of the canonical criteria for identifying synaptic
neurotransmitters, namely detecting its release from stimulated synapses, has yet to be
established for 5HT in taste buds. We have addressed this question by using biosensor
cells that are sensitive to 5HT to reveal transmitter release from mouse taste buds
during sensory stimulation. The results indicate that depolarizing mouse taste cells with
KCl or stimulating them with sweet and bitter tastants elicits 5HT release. Collectively,
these data firmly identify 5HT as a taste cell neurotransmitter.
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Identifying stimulus-evoked release of serotonin from taste buds |
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TopIntroductionIdentifying stimulus-evoked...Ca2+-dependence of serotonin...Summary and conclusionsAcknowledgementsReferences |
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Biosensor cells for detecting 5HT release consisted of Chinese hamster ovary (CHO) cells that stably express 5HT2c receptors (Berg et al., 1994
). These cells, when loaded with
the calcium-sensing dye Fura 2AM and imaged with fluorescent excitation, responded with a
robust increase in [Ca2+]i when stimulated with 5HT
at concentrations 
3 nM. Responses to 5HT were reversibly and reliably blocked by
mianserin but stimulation of endogenous purinergic receptors with ATP was unaffected by
mianserin. Biosensor CHO/5HT2c cells on their own did not generate a
Ca2+ response when they were depolarized with KCl (50 mM), or stimulated
with cycloheximide (a well-established aversive taste compound for rodents) or saccharin
(a sweet tasting compound). Lastly, CHO/5HT2c cells maintained a response to
5HT even if Ca2+ in the medium was replaced with Mg2+,
consistent with the coupling of 5HT2c receptors to intracellular
Ca2+ release. We removed taste buds from vallate papillae of the mouse tongue, transferred them to a recording chamber and manipulated individual CHO/5HT2c biosensor cells, preloaded with Fura 2, up against an isolated taste bud. Mere physical contact between a biosensor cell and a taste bud did not elicit a response. Nor did perfusion with Tyrode solution generate a biosensor response. However, perfusing the chamber with KCl, cycloheximide, or saccharin evoked rapid and repeatable responses from biosensor cells when they were apposed to a taste bud. Responses to these bath-applied stimuli were abolished if the biosensor cell was withdrawn even a few microns from an isolated taste bud, indicating that the taste bud was releasing a compound that triggered biosensor cell activity. Furthermore, biosensor cell responses to KCl, cycloheximide, and saccharin were reversibly blocked by mianserin, verifying 5HT as the compound released from taste buds.
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Ca2+-dependence of serotonin release from stimulated taste bud cells |
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TopIntroductionIdentifying stimulus-evoked...Ca2+-dependence of serotonin...Summary and conclusionsAcknowledgementsReferences |
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We tested whether the release of 5HT from taste buds was Ca2+-dependent. In the case of KCl depolarization, replacing bath Ca2+ with Mg2+ rapidly and reversibly blocked 5HT release from taste buds, as detected with the CHO/5HT2c biosensor. Surprisingly, however, 5HT release elicited by cycloheximide or saccharin was not affected by replacing bath Ca2+ with Mg2+. Cycloheximide and saccharin are known to stimulate intracellular Ca2+ release in taste cells via a cascade of PLCb2 and IP3. Thus, a likely source of Ca2+ for transmitter release elicited by these compounds was an intracellular store. To test this, we isolated taste buds from PLCß2-null mutant mice (Jiang et al., 1997
) and
tested their ability to release 5HT following taste stimulation. Taste buds from
PLCß2-null mice responded to bath-applied KCl, showing normal release of 5HT as
above. However, we were unable to detect 5HT release evoked by cycloheximide or saccharin
from taste buds of mutant mice. |
Summary and conclusions |
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TopIntroductionIdentifying stimulus-evoked...Ca2+-dependence of serotonin...Summary and conclusionsAcknowledgementsReferences |
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Collectively, our findings indicate that 5HT is one of the neurotransmitters released by taste cells in response to gustatory stimulation and to depolarization. The results suggest that whereas depolarization elicits Ca2+-dependent transmitter release from taste cells via Ca2+ influx, certain taste stimuli (namely, cycloheximide and saccharin) evoke transmitter release in response to Ca2+ from intracellular stores.
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Acknowledgements |
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TopIntroductionIdentifying stimulus-evoked...Ca2+-dependence of serotonin...Summary and conclusionsAcknowledgementsReferences |
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Supported in part by NIH/NIDCD grants DC006077 and DC00374 (S.D.R.). We thank K. Berg for the generous donation of CHO cells expressing 5HT2c receptors and D. Wu for kindly providing PLCß2-KO mice.
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References |
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TopIntroductionIdentifying stimulus-evoked...Ca2+-dependence of serotonin...Summary and conclusionsAcknowledgementsReferences |
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