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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