A subset of broadly responsive Type III taste cells contribute to the detection of bitter, sweet and umami stimuli.

Taste receptor cells use multiple signaling pathways to detect chemicals in potential food items. These cells are functionally grouped into different types: Type I cells act as support cells and have glial-like properties; Type II cells detect bitter, sweet, and umami taste stimuli; and Type III cel...

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Main Authors: Debarghya Dutta Banik, Eric D Benfey, Laura E Martin, Kristen E Kay, Gregory C Loney, Amy R Nelson, Zachary C Ahart, Barrett T Kemp, Bailey R Kemp, Ann-Marie Torregrossa, Kathryn F Medler
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-08-01
Series:PLoS Genetics
Online Access:https://doi.org/10.1371/journal.pgen.1008925
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spelling doaj-b64c3f5f5d00430ba7fd6f274fe93d672021-04-21T13:54:22ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042020-08-01168e100892510.1371/journal.pgen.1008925A subset of broadly responsive Type III taste cells contribute to the detection of bitter, sweet and umami stimuli.Debarghya Dutta BanikEric D BenfeyLaura E MartinKristen E KayGregory C LoneyAmy R NelsonZachary C AhartBarrett T KempBailey R KempAnn-Marie TorregrossaKathryn F MedlerTaste receptor cells use multiple signaling pathways to detect chemicals in potential food items. These cells are functionally grouped into different types: Type I cells act as support cells and have glial-like properties; Type II cells detect bitter, sweet, and umami taste stimuli; and Type III cells detect sour and salty stimuli. We have identified a new population of taste cells that are broadly tuned to multiple taste stimuli including bitter, sweet, sour, and umami. The goal of this study was to characterize these broadly responsive (BR) taste cells. We used an IP3R3-KO mouse (does not release calcium (Ca2+) from internal stores in Type II cells when stimulated with bitter, sweet, or umami stimuli) to characterize the BR cells without any potentially confounding input from Type II cells. Using live cell Ca2+ imaging in isolated taste cells from the IP3R3-KO mouse, we found that BR cells are a subset of Type III cells that respond to sour stimuli but also use a PLCβ signaling pathway to respond to bitter, sweet, and umami stimuli. Unlike Type II cells, individual BR cells are broadly tuned and respond to multiple stimuli across different taste modalities. Live cell imaging in a PLCβ3-KO mouse confirmed that BR cells use this signaling pathway to respond to bitter, sweet, and umami stimuli. Short term behavioral assays revealed that BR cells make significant contributions to taste driven behaviors and found that loss of either PLCβ3 in BR cells or IP3R3 in Type II cells caused similar behavioral deficits to bitter, sweet, and umami stimuli. Analysis of c-Fos activity in the nucleus of the solitary tract (NTS) also demonstrated that functional Type II and BR cells are required for normal stimulus induced expression.https://doi.org/10.1371/journal.pgen.1008925
collection DOAJ
language English
format Article
sources DOAJ
author Debarghya Dutta Banik
Eric D Benfey
Laura E Martin
Kristen E Kay
Gregory C Loney
Amy R Nelson
Zachary C Ahart
Barrett T Kemp
Bailey R Kemp
Ann-Marie Torregrossa
Kathryn F Medler
spellingShingle Debarghya Dutta Banik
Eric D Benfey
Laura E Martin
Kristen E Kay
Gregory C Loney
Amy R Nelson
Zachary C Ahart
Barrett T Kemp
Bailey R Kemp
Ann-Marie Torregrossa
Kathryn F Medler
A subset of broadly responsive Type III taste cells contribute to the detection of bitter, sweet and umami stimuli.
PLoS Genetics
author_facet Debarghya Dutta Banik
Eric D Benfey
Laura E Martin
Kristen E Kay
Gregory C Loney
Amy R Nelson
Zachary C Ahart
Barrett T Kemp
Bailey R Kemp
Ann-Marie Torregrossa
Kathryn F Medler
author_sort Debarghya Dutta Banik
title A subset of broadly responsive Type III taste cells contribute to the detection of bitter, sweet and umami stimuli.
title_short A subset of broadly responsive Type III taste cells contribute to the detection of bitter, sweet and umami stimuli.
title_full A subset of broadly responsive Type III taste cells contribute to the detection of bitter, sweet and umami stimuli.
title_fullStr A subset of broadly responsive Type III taste cells contribute to the detection of bitter, sweet and umami stimuli.
title_full_unstemmed A subset of broadly responsive Type III taste cells contribute to the detection of bitter, sweet and umami stimuli.
title_sort subset of broadly responsive type iii taste cells contribute to the detection of bitter, sweet and umami stimuli.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2020-08-01
description Taste receptor cells use multiple signaling pathways to detect chemicals in potential food items. These cells are functionally grouped into different types: Type I cells act as support cells and have glial-like properties; Type II cells detect bitter, sweet, and umami taste stimuli; and Type III cells detect sour and salty stimuli. We have identified a new population of taste cells that are broadly tuned to multiple taste stimuli including bitter, sweet, sour, and umami. The goal of this study was to characterize these broadly responsive (BR) taste cells. We used an IP3R3-KO mouse (does not release calcium (Ca2+) from internal stores in Type II cells when stimulated with bitter, sweet, or umami stimuli) to characterize the BR cells without any potentially confounding input from Type II cells. Using live cell Ca2+ imaging in isolated taste cells from the IP3R3-KO mouse, we found that BR cells are a subset of Type III cells that respond to sour stimuli but also use a PLCβ signaling pathway to respond to bitter, sweet, and umami stimuli. Unlike Type II cells, individual BR cells are broadly tuned and respond to multiple stimuli across different taste modalities. Live cell imaging in a PLCβ3-KO mouse confirmed that BR cells use this signaling pathway to respond to bitter, sweet, and umami stimuli. Short term behavioral assays revealed that BR cells make significant contributions to taste driven behaviors and found that loss of either PLCβ3 in BR cells or IP3R3 in Type II cells caused similar behavioral deficits to bitter, sweet, and umami stimuli. Analysis of c-Fos activity in the nucleus of the solitary tract (NTS) also demonstrated that functional Type II and BR cells are required for normal stimulus induced expression.
url https://doi.org/10.1371/journal.pgen.1008925
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