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Species-Dependent Enhancement of Ovarian Cancer G Protein-Coupled Receptor 1 Activation by Ogerin.
Murakami, Syo; Mochimaru, Yuta; Musha, Shiori; Kojima, Ryotaro; Deai, Masahito; Mogi, Chihiro; Sato, Koichi; Okajima, Fumikazu; Tomura, Hideaki.
Affiliation
  • Murakami S; Laboratory of Cell Signaling Regulation, Department of Life Sciences, School of Agriculture, Meiji University, Kawasaki 214-8571, Japan.
  • Mochimaru Y; Laboratory of Cell Signaling Regulation, Department of Life Sciences, School of Agriculture, Meiji University, Kawasaki 214-8571, Japan.
  • Musha S; Laboratory of Cell Signaling Regulation, Department of Life Sciences, School of Agriculture, Meiji University, Kawasaki 214-8571, Japan.
  • Kojima R; Laboratory of Cell Signaling Regulation, Department of Life Sciences, School of Agriculture, Meiji University, Kawasaki 214-8571, Japan.
  • Deai M; Laboratory of Cell Signaling Regulation, Department of Life Sciences, School of Agriculture, Meiji University, Kawasaki 214-8571, Japan.
  • Mogi C; Laboratory of Integrated Signaling Systems, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi 371-8512, Japan.
  • Sato K; Laboratory of Medical Neuroscience, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi 371-8512, Japan.
  • Okajima F; Laboratory of Pathophysiology, Faculty of Pharmacy, Aomori University, Aomori 030-0943, Japan.
  • Tomura H; Laboratory of Cell Signaling Regulation, Department of Life Sciences, School of Agriculture, Meiji University, Kawasaki 214-8571, Japan, tomurah@meiji.ac.jp.
Zoolog Sci ; 37(2): 103-108, 2020 Apr.
Article in En | MEDLINE | ID: mdl-32282140
Ogerin is a positive allosteric modulator of human and mouse ovarian cancer G protein-coupled receptors (OGR1s). In the present study, we found that ogerin differentially enhances the activation of OGR1 in various animal species. Amino acid residues of OGR1 that are associated with ogerin are conserved among the species. This suggests that other amino acid residues may be involved in the action of ogerin. Chimeric receptors between human and zebrafish OGR1s showed that the amino acid residues that determine the species specificity of ogerin-induced enhancement reside in the transmembrane and/or intracellular regions of OGR1. This result highlights the importance of first verifying the effectiveness of ogerin to the OGR1 of the species of interest at the cellular level prior to analyzing the physiological and pathophysiological roles of OGR1 in the species.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protons / Triazines / Benzyl Alcohols / Receptors, G-Protein-Coupled Limits: Animals / Female / Humans Language: En Journal: Zoolog Sci Journal subject: BIOLOGIA Year: 2020 Document type: Article Affiliation country: Japón Country of publication: Japón

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protons / Triazines / Benzyl Alcohols / Receptors, G-Protein-Coupled Limits: Animals / Female / Humans Language: En Journal: Zoolog Sci Journal subject: BIOLOGIA Year: 2020 Document type: Article Affiliation country: Japón Country of publication: Japón