The monosodium salt of L-glutamate (MSG) is a distinctive taste stimulus found naturally in protein-rich and other foods. A metabotropic receptor for glutamate, mGluR4, is expressed in rat taste buds and appears to function as a taste receptor for MSG. Ligands acting at mGluR4 mimic the taste of MSG. Recently, we have cloned a novel taste-specific form of mGluR4, that has a severely truncated glutamate-binding site. The receptor, taste-mGluR4, is activated only by high concentrations of glutamate, as expected for a taste receptor. We postulate that the altered binding site accounts for some of the unique features of MSG taste. Functional and molecular evidence also exists for ionotropic glutamate receptors (iGluRs) in taste cells. The goal of Project #1 is to use molecular techniques to address whether taste-mGluR4 alone is the taste receptor for MSG for whether activation of iGluRs also contributes to transduction. We will address this question by comparing the functional properties of cloned receptors from taste cells against the functions of taste cells themselves, to identify the key players in MSG taste transduction. Specifically, we will: 1. Test the hypothesis that taste-mGluR4 is a taste receptor for MSG. We will express taste-mGluR4 in CHO cells and measure its response to glutamate, GluR agonists and nucleotides that enhance MSG taste. We will also use Western blots and promoter analyses to test whether taste buds are able to express this novel GluR. 2. Determine if cAMP and/or cGMP are 2nd messengers in glutamate taste transduction as predicted in taste mGluR4 is a taste receptor for MSG. 3. Conduct detailed molecular and functional analyses of a novel iGluR- like sequence we have cloned from taste tissue. We will examine whether this receptor underlies an unusual glutamate-gated ionic conductance found in taste cells, and whether this receptor plays a role in MSG taste. We will also search for additional GluRs in taste tissue in order to achieve a comprehensive description of the taste transduction of MSG. The data from these molecular and cellular approaches will be closely coordinated with results from electrophysiological and behavioral analyses of the same questions, conducted from Projects #2 and #3.

Project Start
2000-03-01
Project End
2001-02-28
Budget Start
Budget End
Support Year
5
Fiscal Year
2000
Total Cost
$239,203
Indirect Cost
Name
University of Miami School of Medicine
Department
Type
DUNS #
City
Miami
State
FL
Country
United States
Zip Code
33146
Chaudhari, Nirupa; Pereira, Elizabeth; Roper, Stephen D (2009) Taste receptors for umami: the case for multiple receptors. Am J Clin Nutr 90:738S-742S
Trubey, Kristina R; Culpepper, Schartess; Maruyama, Yutaka et al. (2006) Tastants evoke cAMP signal in taste buds that is independent of calcium signaling. Am J Physiol Cell Physiol 291:C237-44
Chaudhari, Nirupa; Maruyama, Yutaka; Roper, Stephen et al. (2005) Multiple pathways for signaling glutamate taste in rodents. Chem Senses 30 Suppl 1:i29-30
Kinnamon, Sue C; Lin, Weihong; Ogura, Tatsuya et al. (2005) Downstream signaling effectors for umami taste. Chem Senses 30 Suppl 1:i31-2
Landin, Ana Marie; Kim, Joung Woul; Chaudhari, Nirupa (2005) Liposome-mediated transfection of mature taste cells. J Neurobiol 65:12-21
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Delay, E R; Sewczak, G M; Stapleton, J R et al. (2004) Glutamate taste: Discrimination between the tastes of glutamate agonists and monosodium glutamate in rats. Chem Senses 29:291-9
Abaffy, Tatjana; Trubey, Kristina R; Chaudhari, Nirupa (2003) Adenylyl cyclase expression and modulation of cAMP in rat taste cells. Am J Physiol Cell Physiol 284:C1420-8
Lin, Weihong; Ogura, Tatsuya; Kinnamon, Sue C (2003) Responses to di-sodium guanosine 5'-monophosphate and monosodium L-glutamate in taste receptor cells of rat fungiform papillae. J Neurophysiol 89:1434-9
Stapleton, J R; Luellig, M; Roper, S D et al. (2002) Discrimination between the tastes of sucrose and monosodium glutamate in rats. Chem Senses 27:375-82

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