A Mathematical Model of ATP Secretion by Type II Taste Cells

2021 ◽  
Vol 51 (2) ◽  
pp. 238-244
Author(s):  
S. S. Kolesnikov
2008 ◽  
Vol 132 (6) ◽  
pp. 731-744 ◽  
Author(s):  
Roman A. Romanov ◽  
Olga A. Rogachevskaja ◽  
Alexander A. Khokhlov ◽  
Stanislav S. Kolesnikov

Mammalian type II taste cells release the afferent neurotransmitter adenosine triphosphate (ATP) through ATP-permeable ion channels, most likely to be connexin (Cx) and/or pannexin hemichannels. Here, we show that ion channels responsible for voltage-gated (VG) outward currents in type II cells are ATP permeable and demonstrate a strong correlation between the magnitude of the VG current and the intensity of ATP release. These findings suggest that slowly deactivating ion channels transporting the VG outward currents can also mediate ATP secretion in type II cells. In line with this inference, we studied a dependence of ATP secretion on membrane voltage with a cellular ATP sensor using different pulse protocols. These were designed on the basis of predictions of a model of voltage-dependent transient ATP efflux. Consistently with curves that were simulated for ATP release mediated by ATP-permeable channels deactivating slowly, the bell-like and Langmuir isotherm–like potential dependencies were characteristic of ATP secretion obtained for prolonged and short electrical stimulations of taste cells, respectively. These observations strongly support the idea that ATP is primarily released via slowly deactivating channels. Depolarizing voltage pulses produced negligible Ca2+ transients in the cytoplasm of cells releasing ATP, suggesting that ATP secretion is mainly governed by membrane voltage under our recording conditions. With the proviso that natural connexons and pannexons are kinetically similar to exogenously expressed hemichannels, our findings suggest that VG ATP release in type II cells is primarily mediated by Cx hemichannels.


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 75 (6) ◽  
pp. 1061-1066 ◽  
Author(s):  
Yoichiro SHINDO ◽  
Kana MORISHITA ◽  
Eiichi KOTAKE ◽  
Hirohito MIURA ◽  
Piero CARNINCI ◽  
...  
Keyword(s):  
Type Ii ◽  

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