Previously postulated "ligand-independent" signaling of GPR4 is mediated through proton-sensing mechanisms

Masayuki Tobo, Hideaki Tomura, Chihiro Mogi, Ju Qiang Wang, Jin Peng Liu, Mayumi Komachi, Alatangaole Damirin, Takao Kimura, Naoya Murata, Hitoshi Kurose, Koichi Sato, Fumikazu Okajima

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Abstract

GPR4 was initially identified as a receptor for sphingosylphosphorylcholine and lysophosphatidylcholine; however, lipid actions have not always been confirmed. Instead, ligand-independent actions have sometimes been observed in GPR4- and other OGR1 family receptor-expressing cells. Here, we examined the possible involvement of extracellular protons, which have recently been proposed as another ligand for GPR4. At pH 7.4, the epidermal growth factor-induced extracellular signal-regulated kinase activity was lower in GPR4-transfected RH7777 cells, in association with increased cAMP accumulation, than in vector-transfected cells. The serum response element (SRE)-driven transcriptional activity was also clearly higher in GPR4-expressing HEK293 cells than in vector-transfected cells at pH 7.4. These apparent ligand-independent actions were very small at alkalinic 7.8. The SRE activity was further increased by extracellular acidification in a manner dependent on the G13 protein/Rho signaling pathway in HEK293 cells expressing GPR4 or other OGR1 receptor family members. GPR4-expressing cells also showed a calcineurin-dependent nuclear factor of activated T cell (NFAT) promoter activation at pH 7.4, and this activity was further increased by pH below 7.2 in association with inositol phosphate production. In contrast to the cAMP and SRE responses, however, alkalinization to pH 7.8 hardly affected the high basal activity. Finally, the expression of GPR4 hardly modulated the sphingosylphosphorylcholine- or lysophosphatidylcholine-induced action. These results suggest that an extracellular proton play a role as a ligand in some of previously postulated ligand-independent actions through GPR4 receptors. Moreover, GPR4 may be a multi-functional receptor coupling to Gs, G13, and Gq/11 proteins in response to extracellular acidification.

Original languageEnglish
Pages (from-to)1745-1753
Number of pages9
JournalCellular Signalling
Volume19
Issue number8
DOIs
Publication statusPublished - Aug 1 2007

Fingerprint

Serum Response Element
Protons
Ligands
Lysophosphatidylcholines
HEK293 Cells
G12-G13 GTP-Binding Protein alpha Subunits
Gq-G11 GTP-Binding Protein alpha Subunits
NFATC Transcription Factors
Inositol Phosphates
Calcineurin
Extracellular Signal-Regulated MAP Kinases
Epidermal Growth Factor
Lipids
sphingosine phosphorylcholine

All Science Journal Classification (ASJC) codes

  • Cell Biology

Cite this

Tobo, M., Tomura, H., Mogi, C., Wang, J. Q., Liu, J. P., Komachi, M., ... Okajima, F. (2007). Previously postulated "ligand-independent" signaling of GPR4 is mediated through proton-sensing mechanisms. Cellular Signalling, 19(8), 1745-1753. https://doi.org/10.1016/j.cellsig.2007.03.009

Previously postulated "ligand-independent" signaling of GPR4 is mediated through proton-sensing mechanisms. / Tobo, Masayuki; Tomura, Hideaki; Mogi, Chihiro; Wang, Ju Qiang; Liu, Jin Peng; Komachi, Mayumi; Damirin, Alatangaole; Kimura, Takao; Murata, Naoya; Kurose, Hitoshi; Sato, Koichi; Okajima, Fumikazu.

In: Cellular Signalling, Vol. 19, No. 8, 01.08.2007, p. 1745-1753.

Research output: Contribution to journalArticle

Tobo, M, Tomura, H, Mogi, C, Wang, JQ, Liu, JP, Komachi, M, Damirin, A, Kimura, T, Murata, N, Kurose, H, Sato, K & Okajima, F 2007, 'Previously postulated "ligand-independent" signaling of GPR4 is mediated through proton-sensing mechanisms', Cellular Signalling, vol. 19, no. 8, pp. 1745-1753. https://doi.org/10.1016/j.cellsig.2007.03.009
Tobo, Masayuki ; Tomura, Hideaki ; Mogi, Chihiro ; Wang, Ju Qiang ; Liu, Jin Peng ; Komachi, Mayumi ; Damirin, Alatangaole ; Kimura, Takao ; Murata, Naoya ; Kurose, Hitoshi ; Sato, Koichi ; Okajima, Fumikazu. / Previously postulated "ligand-independent" signaling of GPR4 is mediated through proton-sensing mechanisms. In: Cellular Signalling. 2007 ; Vol. 19, No. 8. pp. 1745-1753.
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