Cell‐type‐dependent action potentials and voltage‐gated currents in mouse fungiform taste buds |
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Authors: | Katsumi Tateno Keita Takeuchi Takashi Kumazawa Kiyonori Yoshii |
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Affiliation: | 1. Graduate school of Life Science and Systems Engineering, Kyushu Institute of Technology, , Kitakyushu‐shi, 808‐0196 Japan;2. Graduate school of Engineering, Saitama Institute of Technology, , Fukara, 369‐0293 Japan |
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Abstract: | Taste receptor cells fire action potentials in response to taste substances to trigger non‐exocytotic neurotransmitter release in type II cells and exocytotic release in type III cells. We investigated possible differences between these action potentials fired by mouse taste receptor cells using in situ whole‐cell recordings, and subsequently we identified their cell types immunologically with cell‐type markers, an IP3 receptor (IP3R3) for type II cells and a SNARE protein (SNAP‐25) for type III cells. Cells not immunoreactive to these antibodies were examined as non‐IRCs. Here, we show that type II cells and type III cells fire action potentials using different ionic mechanisms, and that non‐IRCs also fire action potentials with either of the ionic mechanisms. The width of action potentials was significantly narrower and their afterhyperpolarization was deeper in type III cells than in type II cells. Na+ current density was similar in type II cells and type III cells, but it was significantly smaller in non‐IRCs than in the others. Although outwardly rectifying current density was similar between type II cells and type III cells, tetraethylammonium (TEA) preferentially suppressed the density in type III cells and the majority of non‐IRCs. Our mathematical model revealed that the shape of action potentials depended on the ratio of TEA‐sensitive current density and TEA‐insensitive current one. The action potentials of type II cells and type III cells under physiological conditions are discussed. |
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Keywords: | computer simulation immunohistostaining patch‐clamping taste receptor cells |
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