Odorant Receptor 51E2 Agonist β-ionone Regulates RPE Cell Migration and Proliferation
The odorant receptor 51E2 (OR51E2), which is well-characterized in prostate cancer cells and epidermal pigment cells, was identified for the first time as the most highly expressed OR in human fetal and adult retinal pigment epithelial (RPE) cells. Immunofluorescence staining and Western blot analys...
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Published in | Frontiers in physiology Vol. 8; p. 888 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
30.11.2017
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Subjects | |
Online Access | Get full text |
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Summary: | The odorant receptor 51E2 (OR51E2), which is well-characterized in prostate cancer cells and epidermal pigment cells, was identified for the first time as the most highly expressed OR in human fetal and adult retinal pigment epithelial (RPE) cells. Immunofluorescence staining and Western blot analysis revealed OR51E2 localization throughout the cytosol and in the plasma membrane. Additionally, immunohistochemical staining of diverse layers of the eye showed that the expression of OR51E2 is restricted to the pigment cells of the RPE and choroid. The results of Ca
-imaging experiments demonstrate that activation of OR51E2 triggers a Ca
dependent signal pathway in RPE cells. Downstream signaling of OR51E2 involves the activation of adenylyl cyclase, ERK1/2 and AKT. The activity of these protein kinases likely accounts for the demonstrated increase in the migration and proliferation of RPE cells upon stimulation with the OR51E2 ligand β-ionone. These findings suggest that OR51E2 is involved in the regulation of RPE cell growth. Thus, OR51E2 represents a potential target for the treatment of proliferative disorders. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 This article was submitted to Renal and Epithelial Physiology, a section of the journal Frontiers in Physiology Reviewed by: Jennifer Pluznick, Johns Hopkins School of Medicine, United States; James A. McCormick, Oregon Health and Science University, United States Edited by: Kenneth R. Hallows, Keck School of Medicine of USC, United States These authors have contributed equally to this work. |
ISSN: | 1664-042X 1664-042X |
DOI: | 10.3389/fphys.2017.00888 |