Transgenic Chlamydomonas Expressing Human Transient Receptor Potential Ankyrin 1 (TRPA1) Channels to Assess the Effect of Agonists and Antagonists

Transient receptor potential ankyrin 1 (TRPA1) channel is an ion channel whose gating is controlled by agonists, such as allyl isothiocyanate (AITC), and temperature. Since TRPA1 is associated with various disease symptoms and chemotherapeutic side effects, it is a frequent target of drug developmen...

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Main Authors: Megumi Yoshida, Ryodai Yamamiya, Yuto Shimizu, Kenjiro Yoshimura
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-09-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fphar.2020.578955/full
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author Megumi Yoshida
Ryodai Yamamiya
Yuto Shimizu
Kenjiro Yoshimura
Kenjiro Yoshimura
author_facet Megumi Yoshida
Ryodai Yamamiya
Yuto Shimizu
Kenjiro Yoshimura
Kenjiro Yoshimura
author_sort Megumi Yoshida
collection DOAJ
description Transient receptor potential ankyrin 1 (TRPA1) channel is an ion channel whose gating is controlled by agonists, such as allyl isothiocyanate (AITC), and temperature. Since TRPA1 is associated with various disease symptoms and chemotherapeutic side effects, it is a frequent target of drug development. To facilitate the screening of TRPA1 agonists and antagonists, this study aimed to develop a simple bioassay for TRPA1 activity. To this end, transgenic Chlamydomonas reinhardtii expressing human TRPA1 was constructed. The transformants exhibited positive phototaxis at high temperatures (≥20°C) but negative phototaxis at low temperatures (≤15°C); wild-type cells showed positive phototaxis at all temperatures examined. In the transgenic cells, negative phototaxis was inhibited by TRPA1 antagonists, such as HC030031, A-967079, and AP18, at low temperatures. Negative phototaxis was induced by TRPA1 agonists, such as icilin and AITC, at high temperatures. The effects of these agonists were blocked by TRPA1 antagonists. In wild-type cells, none of these substances had any effects on phototaxis. These results indicate that the action of TRPA1 agonists and antagonists can be readily assessed using the behavior of C. reinhardtii expressing human TRPA1 as an assessment tool.
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spelling doaj.art-52f16b40d3ff422fafb0e06f3678d0fb2022-12-21T23:17:29ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122020-09-011110.3389/fphar.2020.578955578955Transgenic Chlamydomonas Expressing Human Transient Receptor Potential Ankyrin 1 (TRPA1) Channels to Assess the Effect of Agonists and AntagonistsMegumi Yoshida0Ryodai Yamamiya1Yuto Shimizu2Kenjiro Yoshimura3Kenjiro Yoshimura4Department of Machinery and Control Systems, College of Systems Engineering and Science, Shibaura Institute of Technology, Saitama, JapanDepartment of Machinery and Control Systems, College of Systems Engineering and Science, Shibaura Institute of Technology, Saitama, JapanDepartment of Machinery and Control Systems, College of Systems Engineering and Science, Shibaura Institute of Technology, Saitama, JapanDepartment of Machinery and Control Systems, College of Systems Engineering and Science, Shibaura Institute of Technology, Saitama, JapanBio-Inteligence for Well Being, Shibaura Institute of Technology, Saitama, JapanTransient receptor potential ankyrin 1 (TRPA1) channel is an ion channel whose gating is controlled by agonists, such as allyl isothiocyanate (AITC), and temperature. Since TRPA1 is associated with various disease symptoms and chemotherapeutic side effects, it is a frequent target of drug development. To facilitate the screening of TRPA1 agonists and antagonists, this study aimed to develop a simple bioassay for TRPA1 activity. To this end, transgenic Chlamydomonas reinhardtii expressing human TRPA1 was constructed. The transformants exhibited positive phototaxis at high temperatures (≥20°C) but negative phototaxis at low temperatures (≤15°C); wild-type cells showed positive phototaxis at all temperatures examined. In the transgenic cells, negative phototaxis was inhibited by TRPA1 antagonists, such as HC030031, A-967079, and AP18, at low temperatures. Negative phototaxis was induced by TRPA1 agonists, such as icilin and AITC, at high temperatures. The effects of these agonists were blocked by TRPA1 antagonists. In wild-type cells, none of these substances had any effects on phototaxis. These results indicate that the action of TRPA1 agonists and antagonists can be readily assessed using the behavior of C. reinhardtii expressing human TRPA1 as an assessment tool.https://www.frontiersin.org/article/10.3389/fphar.2020.578955/fullTRP channelChlamydomonas reinhardtiiTRPA1phototaxisbioassaydrug development
spellingShingle Megumi Yoshida
Ryodai Yamamiya
Yuto Shimizu
Kenjiro Yoshimura
Kenjiro Yoshimura
Transgenic Chlamydomonas Expressing Human Transient Receptor Potential Ankyrin 1 (TRPA1) Channels to Assess the Effect of Agonists and Antagonists
Frontiers in Pharmacology
TRP channel
Chlamydomonas reinhardtii
TRPA1
phototaxis
bioassay
drug development
title Transgenic Chlamydomonas Expressing Human Transient Receptor Potential Ankyrin 1 (TRPA1) Channels to Assess the Effect of Agonists and Antagonists
title_full Transgenic Chlamydomonas Expressing Human Transient Receptor Potential Ankyrin 1 (TRPA1) Channels to Assess the Effect of Agonists and Antagonists
title_fullStr Transgenic Chlamydomonas Expressing Human Transient Receptor Potential Ankyrin 1 (TRPA1) Channels to Assess the Effect of Agonists and Antagonists
title_full_unstemmed Transgenic Chlamydomonas Expressing Human Transient Receptor Potential Ankyrin 1 (TRPA1) Channels to Assess the Effect of Agonists and Antagonists
title_short Transgenic Chlamydomonas Expressing Human Transient Receptor Potential Ankyrin 1 (TRPA1) Channels to Assess the Effect of Agonists and Antagonists
title_sort transgenic chlamydomonas expressing human transient receptor potential ankyrin 1 trpa1 channels to assess the effect of agonists and antagonists
topic TRP channel
Chlamydomonas reinhardtii
TRPA1
phototaxis
bioassay
drug development
url https://www.frontiersin.org/article/10.3389/fphar.2020.578955/full
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