FXYD6, a Na,K-ATPase Regulator, Is Expressed in Type II Taste Cells

2011 ◽  
Vol 75 (6) ◽  
pp. 1061-1066 ◽  
Author(s):  
Yoichiro SHINDO ◽  
Kana MORISHITA ◽  
Eiichi KOTAKE ◽  
Hirohito MIURA ◽  
Piero CARNINCI ◽  
...  
Keyword(s):  
Type Ii ◽  
PLoS ONE ◽  
2012 ◽  
Vol 7 (8) ◽  
pp. e43140 ◽  
Author(s):  
Pu Feng ◽  
Hang Zhao ◽  
Jinghua Chai ◽  
Liquan Huang ◽  
Hong Wang

Author(s):  
R. A. Romanov ◽  
N. V. Kabanova ◽  
S. L. Malkin ◽  
S. S. Kolesnikov

2019 ◽  
Author(s):  
Debarghya Dutta Banik ◽  
Eric D. Benfey ◽  
Laura E. Martin ◽  
Kristen E. Kay ◽  
Gregory C. Loney ◽  
...  

ABSTRACTTaste 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 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 PLCβ3 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 a PLCβ3 signaling pathway to generate Ca2+ signals to bitter, sweet and umami stimuli. Analysis of c-Fos activity in the nucleus of the solitary tract (NTS) and short term behavioral assays revealed that BR cells make significant contributions to taste.


2011 ◽  
Vol 59 (5) ◽  
pp. 530-539 ◽  
Author(s):  
Michelle R. Rebello ◽  
Adem Aktas ◽  
Kathryn F. Medler

eNeuro ◽  
2020 ◽  
Vol 7 (1) ◽  
pp. ENEURO.0339-19.2020 ◽  
Author(s):  
Eric D. Larson ◽  
Aurelie Vandenbeuch ◽  
Catherine B. Anderson ◽  
Sue C. Kinnamon
Keyword(s):  
Type Ii ◽  

2013 ◽  
Vol 353 (3) ◽  
pp. 391-398 ◽  
Author(s):  
Takeshi Kotani ◽  
Takashi Toyono ◽  
Yuji Seta ◽  
Ayae Kitou ◽  
Shinji Kataoka ◽  
...  
Keyword(s):  
Type Ii ◽  
Type Iii ◽  

Author(s):  
Máire E. Doyle ◽  
Ashley Appleton ◽  
Qing-Rong Liu ◽  
Qin Yao ◽  
Caio Henrique Mazucanti ◽  
...  
Keyword(s):  
Type Ii ◽  

2010 ◽  
Vol 104 (2) ◽  
pp. 896-901 ◽  
Author(s):  
Yoshihiro Murata ◽  
Toshiaki Yasuo ◽  
Ryusuke Yoshida ◽  
Kunihiko Obata ◽  
Yuchio Yanagawa ◽  
...  

Only some taste cells fire action potentials in response to sapid stimuli. Type II taste cells express many taste transduction molecules but lack well-elaborated synapses, bringing into question the functional significance of action potentials in these cells. We examined the dependence of adenosine triphosphate (ATP) transmitter release from taste cells on action potentials. To identify type II taste cells we used mice expressing a green fluorescence protein (GFP) transgene from the α-gustducin promoter. Action potentials were recorded by an electrode basolaterally attached to a single GFP-positive taste cell. We monitored ATP release from gustducin-expressing taste cells by collecting the electrode solution immediately after tastant-stimulated action potentials and using a luciferase assay to quantify ATP. Stimulation of gustducin-expressing taste cells with saccharin, quinine, or glutamate on the apical membrane increased ATP levels in the electrode solution; the amount of ATP depended on the firing rate. Increased spontaneous firing rates also induced ATP release from gustducin-expressing taste cells. ATP release from gustducin-expressing taste cells was depressed by tetrodotoxin and inhibited below the detection limit by carbenoxolone. Our data support the hypothesis that action potentials in taste cells responsive to sweet, bitter, or umami tastants enhance ATP release through pannexin 1, not connexin-based hemichannels.


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