TDAG8 is a proton-sensing and psychosine-sensitive G-protein-coupled receptor

Ju Qiang Wang, Junko Kon, Chihiro Mogi, Masayuki Tobo, Alatangaole Damirin, Koichi Sato, Mayumi Komachi, Enkhzol Malchinkhuu, Naoya Murata, Takao Kimura, Atsushi Kuwabara, Kaori Wakamatsu, Hideki Koizumi, Toshimitsu Uedell, Gozoh Tsujimoto, Hitoshi Kurose, Takashi Sato, Akihiro Harada, Norihiko Misawa, Hideaki TomuraFumikazu Okajima

Research output: Contribution to journalArticle

146 Citations (Scopus)

Abstract

T cell death-associated gene 8 (TDAG8) has been reported to be a receptor for psychosine. Ovarian cancer G-protein-coupled receptor 1 (OGR1) and GPR4, G-protein-coupled receptors (GPCRs) closely related to TDAG8, however, have recently been identified as proton-sensing or extracellular pH-responsive GPCRs that stimulate inositol phosphate and cAMP production, respectively. In the present study, we examined whether TDAG8 senses extracellular pH change. In the several cell types that were transfected with TDAG8 cDNA, cAMP was markedly accumulated in response to neutral to acidic extracellular pH, with a peak response at approximately pH 7.0-6.5. The pH effect was inhibited by copper ions and was reduced or lost in cells expressing mutated TDAG8 in which histidine residues were changed to phenylalanine. In the membrane fractions prepared from TDAG8-transfected cells, guanosine 5′-O-(3-thiotriphosphate) binding activity and adenylyl cyclase activity were remarkably stimulated in response to neutral and acidic pH. The concentration-dependent effect of extracellular protons on cAMP accumulation was shifted to the right in the presence of psychosine. The inhibitory psychosine effect was also observed for pH-dependent actions in OGR1- and GPR4-expressing cells but not for prostaglandin E 2- and sphingosine 1-phosphate-induced actions in any pH in native and sphingosine 1-phosphate receptor-expressing cells. Glucosylsphingosine and sphingosylphosphorylcholine similarly inhibited the pH-dependent action, although to a lesser extent. Psychosine-sensitive and pH-dependent cAMP accumulation was also observed in mouse thymocytes. We concluded that TDAG8 is one of the proton-sensing GPCRs coupling to adenylyl cyclase and psychosine, and its related lysosphingolipids behave as if they were antagonists against protein-sensing receptors, including TDAG8, GPR4, and OGR1.

Original languageEnglish
Pages (from-to)45626-45633
Number of pages8
JournalJournal of Biological Chemistry
Volume279
Issue number44
DOIs
Publication statusPublished - Oct 29 2004

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Psychosine
T-cells
Cell death
G-Protein-Coupled Receptors
Protons
Cell Death
Genes
T-Lymphocytes
Ovarian Neoplasms
Adenylyl Cyclases
Lysosphingolipid Receptors
pH effects
Guanosine 5'-O-(3-Thiotriphosphate)
Sphingolipids
Inositol Phosphates
Prostaglandins E
Phenylalanine
Histidine
Copper
Thymocytes

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Molecular Biology
  • Cell Biology

Cite this

Wang, J. Q., Kon, J., Mogi, C., Tobo, M., Damirin, A., Sato, K., ... Okajima, F. (2004). TDAG8 is a proton-sensing and psychosine-sensitive G-protein-coupled receptor. Journal of Biological Chemistry, 279(44), 45626-45633. https://doi.org/10.1074/jbc.M406966200

TDAG8 is a proton-sensing and psychosine-sensitive G-protein-coupled receptor. / Wang, Ju Qiang; Kon, Junko; Mogi, Chihiro; Tobo, Masayuki; Damirin, Alatangaole; Sato, Koichi; Komachi, Mayumi; Malchinkhuu, Enkhzol; Murata, Naoya; Kimura, Takao; Kuwabara, Atsushi; Wakamatsu, Kaori; Koizumi, Hideki; Uedell, Toshimitsu; Tsujimoto, Gozoh; Kurose, Hitoshi; Sato, Takashi; Harada, Akihiro; Misawa, Norihiko; Tomura, Hideaki; Okajima, Fumikazu.

In: Journal of Biological Chemistry, Vol. 279, No. 44, 29.10.2004, p. 45626-45633.

Research output: Contribution to journalArticle

Wang, JQ, Kon, J, Mogi, C, Tobo, M, Damirin, A, Sato, K, Komachi, M, Malchinkhuu, E, Murata, N, Kimura, T, Kuwabara, A, Wakamatsu, K, Koizumi, H, Uedell, T, Tsujimoto, G, Kurose, H, Sato, T, Harada, A, Misawa, N, Tomura, H & Okajima, F 2004, 'TDAG8 is a proton-sensing and psychosine-sensitive G-protein-coupled receptor', Journal of Biological Chemistry, vol. 279, no. 44, pp. 45626-45633. https://doi.org/10.1074/jbc.M406966200
Wang, Ju Qiang ; Kon, Junko ; Mogi, Chihiro ; Tobo, Masayuki ; Damirin, Alatangaole ; Sato, Koichi ; Komachi, Mayumi ; Malchinkhuu, Enkhzol ; Murata, Naoya ; Kimura, Takao ; Kuwabara, Atsushi ; Wakamatsu, Kaori ; Koizumi, Hideki ; Uedell, Toshimitsu ; Tsujimoto, Gozoh ; Kurose, Hitoshi ; Sato, Takashi ; Harada, Akihiro ; Misawa, Norihiko ; Tomura, Hideaki ; Okajima, Fumikazu. / TDAG8 is a proton-sensing and psychosine-sensitive G-protein-coupled receptor. In: Journal of Biological Chemistry. 2004 ; Vol. 279, No. 44. pp. 45626-45633.
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abstract = "T cell death-associated gene 8 (TDAG8) has been reported to be a receptor for psychosine. Ovarian cancer G-protein-coupled receptor 1 (OGR1) and GPR4, G-protein-coupled receptors (GPCRs) closely related to TDAG8, however, have recently been identified as proton-sensing or extracellular pH-responsive GPCRs that stimulate inositol phosphate and cAMP production, respectively. In the present study, we examined whether TDAG8 senses extracellular pH change. In the several cell types that were transfected with TDAG8 cDNA, cAMP was markedly accumulated in response to neutral to acidic extracellular pH, with a peak response at approximately pH 7.0-6.5. The pH effect was inhibited by copper ions and was reduced or lost in cells expressing mutated TDAG8 in which histidine residues were changed to phenylalanine. In the membrane fractions prepared from TDAG8-transfected cells, guanosine 5′-O-(3-thiotriphosphate) binding activity and adenylyl cyclase activity were remarkably stimulated in response to neutral and acidic pH. The concentration-dependent effect of extracellular protons on cAMP accumulation was shifted to the right in the presence of psychosine. The inhibitory psychosine effect was also observed for pH-dependent actions in OGR1- and GPR4-expressing cells but not for prostaglandin E 2- and sphingosine 1-phosphate-induced actions in any pH in native and sphingosine 1-phosphate receptor-expressing cells. Glucosylsphingosine and sphingosylphosphorylcholine similarly inhibited the pH-dependent action, although to a lesser extent. Psychosine-sensitive and pH-dependent cAMP accumulation was also observed in mouse thymocytes. We concluded that TDAG8 is one of the proton-sensing GPCRs coupling to adenylyl cyclase and psychosine, and its related lysosphingolipids behave as if they were antagonists against protein-sensing receptors, including TDAG8, GPR4, and OGR1.",
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T1 - TDAG8 is a proton-sensing and psychosine-sensitive G-protein-coupled receptor

AU - Wang, Ju Qiang

AU - Kon, Junko

AU - Mogi, Chihiro

AU - Tobo, Masayuki

AU - Damirin, Alatangaole

AU - Sato, Koichi

AU - Komachi, Mayumi

AU - Malchinkhuu, Enkhzol

AU - Murata, Naoya

AU - Kimura, Takao

AU - Kuwabara, Atsushi

AU - Wakamatsu, Kaori

AU - Koizumi, Hideki

AU - Uedell, Toshimitsu

AU - Tsujimoto, Gozoh

AU - Kurose, Hitoshi

AU - Sato, Takashi

AU - Harada, Akihiro

AU - Misawa, Norihiko

AU - Tomura, Hideaki

AU - Okajima, Fumikazu

PY - 2004/10/29

Y1 - 2004/10/29

N2 - T cell death-associated gene 8 (TDAG8) has been reported to be a receptor for psychosine. Ovarian cancer G-protein-coupled receptor 1 (OGR1) and GPR4, G-protein-coupled receptors (GPCRs) closely related to TDAG8, however, have recently been identified as proton-sensing or extracellular pH-responsive GPCRs that stimulate inositol phosphate and cAMP production, respectively. In the present study, we examined whether TDAG8 senses extracellular pH change. In the several cell types that were transfected with TDAG8 cDNA, cAMP was markedly accumulated in response to neutral to acidic extracellular pH, with a peak response at approximately pH 7.0-6.5. The pH effect was inhibited by copper ions and was reduced or lost in cells expressing mutated TDAG8 in which histidine residues were changed to phenylalanine. In the membrane fractions prepared from TDAG8-transfected cells, guanosine 5′-O-(3-thiotriphosphate) binding activity and adenylyl cyclase activity were remarkably stimulated in response to neutral and acidic pH. The concentration-dependent effect of extracellular protons on cAMP accumulation was shifted to the right in the presence of psychosine. The inhibitory psychosine effect was also observed for pH-dependent actions in OGR1- and GPR4-expressing cells but not for prostaglandin E 2- and sphingosine 1-phosphate-induced actions in any pH in native and sphingosine 1-phosphate receptor-expressing cells. Glucosylsphingosine and sphingosylphosphorylcholine similarly inhibited the pH-dependent action, although to a lesser extent. Psychosine-sensitive and pH-dependent cAMP accumulation was also observed in mouse thymocytes. We concluded that TDAG8 is one of the proton-sensing GPCRs coupling to adenylyl cyclase and psychosine, and its related lysosphingolipids behave as if they were antagonists against protein-sensing receptors, including TDAG8, GPR4, and OGR1.

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