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

被引:42
作者
Banik, Debarghya Dutta [1 ]
Benfey, Eric D. [1 ]
Martin, Laura E. [2 ]
Kay, Kristen E. [2 ]
Loney, Gregory C. [2 ]
Nelson, Amy R. [1 ]
Ahart, Zachary C. [1 ]
Kemp, Barrett T. [1 ]
Kemp, Bailey R. [1 ]
Torregrossa, Ann-Marie [2 ,3 ]
Medler, Kathryn F. [1 ,3 ]
机构
[1] Univ Buffalo, Dept Biol Sci, Buffalo, NY 14260 USA
[2] Univ Buffalo, Dept Psychol, Buffalo, NY USA
[3] Univ Buffalo, Ctr Ingest Behav Res, Buffalo, NY 14260 USA
关键词
REGIONAL EXPRESSION PATTERNS; FOS-LIKE IMMUNOREACTIVITY; SOLITARY TRACT; RECEPTOR-CELLS; COINCIDENCE DETECTION; MONOSODIUM GLUTAMATE; ROSTRAL NUCLEUS; GUSTATORY CELLS; CALCIUM LEVELS; POPULATIONS;
D O I
10.1371/journal.pgen.1008925
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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 IP(3)R3-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 Ca(2+)imaging in isolated taste cells from the IP(3)R3-KO mouse, we found that BR cells are a subset of Type III cells that respond to sour stimuli but also use a PLC beta 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 PLC beta 3-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 PLC beta 3 in BR cells or IP(3)R3 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. Author summary We use our taste system to decide if we are going to consume or reject a potential food item. This is critical for survival, as we need energy to live but also need to avoid potentially toxic compounds. Therefore, it is important to understand how the taste cells in our mouth detect the chemicals in food and send a message to our brain. Signals from the taste cells form a code that conveys information about the nature of the potential food item to the brain. How this taste coding works is not well understood. Currently, it is thought that taste cells are primarily selective for each taste stimuli and only detect either bitter, sweet, sour, salt, or umami (amino acids) compounds. Our study describes a new population of taste cells that can detect multiple types of stimuli, including chemicals from different taste qualities. Thus, taste cells can be either selective or generally responsive to stimuli which is similar to the cells in the brain that process taste information. The presence of these broadly responsive taste cells provides new insight into how taste information is sent to the brain for processing.
引用
收藏
页数:31
相关论文
共 116 条
[1]  
Abstracts from The Academy of Breastfeeding Medicine, 2015, BREASTFEED MED, V10, pS1
[2]   Differential spatial representation of taste modalities in the rat gustatory cortex [J].
Accolla, Riccardo ;
Bathellier, Brice ;
Petersen, Carl C. H. ;
Carleton, Alan .
JOURNAL OF NEUROSCIENCE, 2007, 27 (06) :1396-1404
[3]   A novel family of mammalian taste receptors [J].
Adler, E ;
Hoon, MA ;
Mueller, KL ;
Chandrashekar, J ;
Ryba, NJP ;
Zuker, CS .
CELL, 2000, 100 (06) :693-702
[4]   Coincidence Detection of Single-Photon Responses in the Inner Retina at the Sensitivity Limit of Vision [J].
Ala-Laurila, Petri ;
Rieke, Fred .
CURRENT BIOLOGY, 2014, 24 (24) :2888-2898
[5]  
[Anonymous], 2018, DTSCH ARZTEBL, V115, pA
[6]  
[Anonymous], 2012, AM J PHYSL ENDOCRINO, V303, pE410
[7]   IP3 receptor type 3 and PLCβ2 are co-expressed with taste receptors T1R and T2R in rat taste bud cells [J].
Asano-Miyoshi, M ;
Abe, K ;
Emori, Y .
CHEMICAL SENSES, 2001, 26 (03) :259-265
[8]   The neural representation of taste quality at the periphery [J].
Barretto, Robert P. J. ;
Gillis-Smith, Sarah ;
Chandrashekar, Jayaram ;
Yarmolinsky, David A. ;
Schnitzer, Mark J. ;
Ryba, Nicholas J. P. ;
Zuker, Charles S. .
NATURE, 2015, 517 (7534) :373-U511
[9]   Response Latency to Lingual Taste Stimulation Distinguishes Neuron Types Within the Geniculate Ganglion [J].
Breza, Joseph M. ;
Nikonov, Alexandre A. ;
Contreras, Robert J. .
JOURNAL OF NEUROPHYSIOLOGY, 2010, 103 (04) :1771-1784
[10]   It takes two-coincidence coding within the dual olfactory pathway of the honeybee [J].
Brill, Martin F. ;
Meyer, Anneke ;
Roessler, Wolfgang .
FRONTIERS IN PHYSIOLOGY, 2015, 6