Journal article

The actions of relaxin family peptides on signal transduction pathways activated by the relaxin family peptide receptor RXFP4

SY Ang, DS Hutchinson, BA Evans, MA Hossain, N Patil, RAD Bathgate, M Kocan, RJ Summers

Naunyn Schmiedeberg S Archives of Pharmacology | SPRINGER | Published : 2017

Abstract

The relaxin family peptide receptor 4 (RXFP4) is a G protein-coupled receptor (GPCR) expressed in the colorectum with emerging roles in metabolism and appetite regulation. It is activated by its cognate ligand insulin-like peptide 5 (INSL5) that is expressed in enteroendocrine L cells in the gut. Whether other evolutionarily related peptides such as relaxin-2, relaxin-3, or INSL3 activate RXFP4 signal transduction mechanisms with a pattern similar to or distinct from INSL5 is still unclear. In this study, we compare the signaling pathways activated by various relaxin family peptides to INSL5. We found that, like INSL5, relaxin-3 activated ERK1/2, p38MAPK, Akt, and S6RP phosphorylations leadi..

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University of Melbourne Researchers

Grants

Awarded by Faculty of Pharmacy and Pharmaceutical Sciences, University of Alberta


Funding Acknowledgements

This work is supported by an Australian National Health and Medical Research Council (NHMRC) program grant (1055134; RJS). DSH is supported by a NHMRC Career Development Fellowship (545952). SYA is supported by a Faculty of Pharmacy and Pharmaceutical Sciences, Monash University Postgraduate Scholarship. Research at the Florey was supported by an ARC Linkage grant to RADB and MAH (LP120100654) and by the Victorian Government Operational Infrastructure Support Program. RADB is supported by an NHMRC Research Fellowship (1042650).