論文 - 詳細
| RRC ID | 38911 |
|---|---|
| 著者 | Ichijo Y, Mochimaru Y, Azuma M, Satou K, Negishi J, Nakakura T, Oshima N, Mogi C, Sato K, Matsuda K, Okajima F, Tomura H. |
| タイトル | Two zebrafish G2A homologs activate multiple intracellular signaling pathways in acidic environment. |
| ジャーナル | Biochem Biophys Res Commun |
| Abstract |
Human G2A is activated by various stimuli such as lysophosphatidylcholine (LPC), 9-hydroxyoctadecadienoic acid (9-HODE), and protons. The receptor is coupled to multiple intracellular signaling pathways, including the Gs-protein/cAMP/CRE, G12/13-protein/Rho/SRE, and Gq-protein/phospholipase C/NFAT pathways. In the present study, we examined whether zebrafish G2A homologs (zG2A-a and zG2A-b) could respond to these stimuli and activate multiple intracellular signaling pathways. We also examined whether histidine residue and basic amino acid residue in the N-terminus of the homologs also play roles similar to those played by human G2A residues if the homologs sense protons. We found that the zG2A-a showed the high CRE, SRE, and NFAT activities, however, zG2A-b showed only the high SRE activity under a pH of 8.0. Extracellular acidification from pH 7.4 to 6.3 ameliorated these activities in zG2A-a-expressing cells. On the other hand, acidification ameliorated the SRE activity but not the CRE and NFAT activities in zG2A-b-expressing cells. LPC or 9-HODE did not modify any activity of either homolog. The substitution of histidine residue at the 174(th) position from the N-terminus of zG2A-a to asparagine residue attenuated proton-induced CRE and NFAT activities but not SRE activity. The substitution of arginine residue at the 32nd position from the N-terminus of zG2A-a to the alanine residue also attenuated its high and the proton-induced CRE and NFAT activities. On the contrary, the substitution did not attenuate SRE activity. The substitution of the arginine residue at the 10th position from the N-terminus of zG2A-b to the alanine residue also did not attenuate its high or the proton-induced SRE activity. These results indicate that zebrafish G2A homologs were activated by protons but not by LPC and 9-HODE, and the activation mechanisms of the homologs were similar to those of human G2A. |
| 巻・号 | 469(1) |
| ページ | 81-86 |
| 公開日 | 2016-1-1 |
| DOI | 10.1016/j.bbrc.2015.11.075 |
| PII | S0006-291X(15)30944-X |
| PMID | 26614909 |
| MeSH | Amino Acid Sequence Animals Cell Cycle Proteins / chemistry* Cell Cycle Proteins / metabolism* HEK293 Cells Humans Hydrogen-Ion Concentration* Intracellular Fluid / chemistry Intracellular Fluid / metabolism Molecular Sequence Data Protein Binding Receptors, G-Protein-Coupled / chemistry* Receptors, G-Protein-Coupled / metabolism* Signal Transduction / physiology* Structure-Activity Relationship Zebrafish / metabolism* |
| IF | 2.985 |
| 引用数 | 3 |
| WOS 分野 | BIOCHEMISTRY & MOLECULAR BIOLOGY BIOPHYSICS |
| オルトメトリクス指標 |
オルトメトリクス指標項目
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| 最多言及媒体 | X(Twitter) |
| 各媒体での言及数の合計 | 1 |
| 過去6か月間でのオルトメトリクス指標の変動値 | 0.0 |
| リソース情報 | |
| ヒト・動物細胞 | 293T(RCB2202) |