Dr RAVINDER ANAND-IVELL RAVINDER.ANAND-IVELL@NOTTINGHAM.AC.UK
ASSOCIATE PROFESSOR
Relaxin signalling in THP-1 cells uses a novel phosphotyrosine-dependent pathway
Anand-Ivell, Ravinder; Heng, Kee; Bartsch, Olaf; Ivell, Richard
Authors
Kee Heng
Olaf Bartsch
Richard Ivell
Abstract
The heterodimeric peptide hormone relaxin acts through the novel G-protein coupled receptor LGR7 to elicit the production of cAMP in the human monocyte cell line THP-1. The very small number of receptors on the cell surface, and the lack of response in cell membranes imply the involvement of a cytoplasmic signal amplification process. Here we show that this process comprises a novel and specific tyrosine kinase activity close to the receptor, and involves neither protein kinase A, mitogen-activated protein kinase, nor phosphoinositide-3 kinase activities as major upstream components. Furthermore, this novel involvement of a tyrosine kinase activity is cell-type dependent, being largely absent from LGR7-transfected HEK293T cells, and receptor-dependent; vasoactive intestinal peptide or isoproterenol signalling in the same cells does not require this tyrosine kinase activity. © 2007 Elsevier Ireland Ltd. All rights reserved.
Citation
Anand-Ivell, R., Heng, K., Bartsch, O., & Ivell, R. (2007). Relaxin signalling in THP-1 cells uses a novel phosphotyrosine-dependent pathway. Molecular and Cellular Endocrinology, 272(1-2), 1-13. https://doi.org/10.1016/j.mce.2007.04.001
Journal Article Type | Article |
---|---|
Acceptance Date | Apr 2, 2007 |
Online Publication Date | Apr 6, 2007 |
Publication Date | Jun 30, 2007 |
Deposit Date | Jun 15, 2021 |
Journal | Molecular and Cellular Endocrinology |
Print ISSN | 0303-7207 |
Electronic ISSN | 1872-8057 |
Publisher | Elsevier |
Peer Reviewed | Peer Reviewed |
Volume | 272 |
Issue | 1-2 |
Pages | 1-13 |
DOI | https://doi.org/10.1016/j.mce.2007.04.001 |
Public URL | https://nottingham-repository.worktribe.com/output/3176604 |
Publisher URL | https://www.sciencedirect.com/science/article/abs/pii/S0303720707001505?via%3Dihub |
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