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Elabela-Apelin Receptor Signaling Pathway is Functional in Mammalian Systems
Elabela (ELA) or Toddler is a recently discovered hormone which is required for normal development of heart and vasculature through activation of apelin receptor (APJ), a G protein-coupled receptor (GPCR), in zebrafish. The present study explores whether the ELA-APJ signaling pathway is functional i...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313117/ https://www.ncbi.nlm.nih.gov/pubmed/25639753 http://dx.doi.org/10.1038/srep08170 |
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author | Wang, Zhi Yu, Daozhan Wang, Mengqiao Wang, Qilong Kouznetsova, Jennifer Yang, Rongze Qian, Kun Wu, Wenjun Shuldiner, Alan Sztalryd, Carole Zou, Minghui Zheng, Wei Gong, Da-Wei |
author_facet | Wang, Zhi Yu, Daozhan Wang, Mengqiao Wang, Qilong Kouznetsova, Jennifer Yang, Rongze Qian, Kun Wu, Wenjun Shuldiner, Alan Sztalryd, Carole Zou, Minghui Zheng, Wei Gong, Da-Wei |
author_sort | Wang, Zhi |
collection | PubMed |
description | Elabela (ELA) or Toddler is a recently discovered hormone which is required for normal development of heart and vasculature through activation of apelin receptor (APJ), a G protein-coupled receptor (GPCR), in zebrafish. The present study explores whether the ELA-APJ signaling pathway is functional in the mammalian system. Using reverse-transcription PCR, we found that ELA is restrictedly expressed in human pluripotent stem cells and adult kidney whereas APJ is more widely expressed. We next studied ELA-APJ signaling pathway in reconstituted mammalian cell systems. Addition of ELA to HEK293 cells over-expressing GFP-AJP fusion protein resulted in rapid internalization of the fusion receptor. In Chinese hamster ovarian (CHO) cells over-expressing human APJ, ELA suppresses cAMP production with EC(50) of 11.1 nM, stimulates ERK1/2 phosphorylation with EC(50) of 14.3 nM and weakly induces intracellular calcium mobilization. Finally, we tested ELA biological function in human umbilical vascular endothelial cells and showed that ELA induces angiogenesis and relaxes mouse aortic blood vessel in a dose-dependent manner through a mechanism different from apelin. Collectively, we demonstrate that the ELA-AJP signaling pathways are functional in mammalian systems, indicating that ELA likely serves as a hormone regulating the circulation system in adulthood as well as in embryonic development. |
format | Online Article Text |
id | pubmed-4313117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43131172015-02-11 Elabela-Apelin Receptor Signaling Pathway is Functional in Mammalian Systems Wang, Zhi Yu, Daozhan Wang, Mengqiao Wang, Qilong Kouznetsova, Jennifer Yang, Rongze Qian, Kun Wu, Wenjun Shuldiner, Alan Sztalryd, Carole Zou, Minghui Zheng, Wei Gong, Da-Wei Sci Rep Article Elabela (ELA) or Toddler is a recently discovered hormone which is required for normal development of heart and vasculature through activation of apelin receptor (APJ), a G protein-coupled receptor (GPCR), in zebrafish. The present study explores whether the ELA-APJ signaling pathway is functional in the mammalian system. Using reverse-transcription PCR, we found that ELA is restrictedly expressed in human pluripotent stem cells and adult kidney whereas APJ is more widely expressed. We next studied ELA-APJ signaling pathway in reconstituted mammalian cell systems. Addition of ELA to HEK293 cells over-expressing GFP-AJP fusion protein resulted in rapid internalization of the fusion receptor. In Chinese hamster ovarian (CHO) cells over-expressing human APJ, ELA suppresses cAMP production with EC(50) of 11.1 nM, stimulates ERK1/2 phosphorylation with EC(50) of 14.3 nM and weakly induces intracellular calcium mobilization. Finally, we tested ELA biological function in human umbilical vascular endothelial cells and showed that ELA induces angiogenesis and relaxes mouse aortic blood vessel in a dose-dependent manner through a mechanism different from apelin. Collectively, we demonstrate that the ELA-AJP signaling pathways are functional in mammalian systems, indicating that ELA likely serves as a hormone regulating the circulation system in adulthood as well as in embryonic development. Nature Publishing Group 2015-02-02 /pmc/articles/PMC4313117/ /pubmed/25639753 http://dx.doi.org/10.1038/srep08170 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wang, Zhi Yu, Daozhan Wang, Mengqiao Wang, Qilong Kouznetsova, Jennifer Yang, Rongze Qian, Kun Wu, Wenjun Shuldiner, Alan Sztalryd, Carole Zou, Minghui Zheng, Wei Gong, Da-Wei Elabela-Apelin Receptor Signaling Pathway is Functional in Mammalian Systems |
title | Elabela-Apelin Receptor Signaling Pathway is Functional in Mammalian Systems |
title_full | Elabela-Apelin Receptor Signaling Pathway is Functional in Mammalian Systems |
title_fullStr | Elabela-Apelin Receptor Signaling Pathway is Functional in Mammalian Systems |
title_full_unstemmed | Elabela-Apelin Receptor Signaling Pathway is Functional in Mammalian Systems |
title_short | Elabela-Apelin Receptor Signaling Pathway is Functional in Mammalian Systems |
title_sort | elabela-apelin receptor signaling pathway is functional in mammalian systems |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313117/ https://www.ncbi.nlm.nih.gov/pubmed/25639753 http://dx.doi.org/10.1038/srep08170 |
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