Journal article
H3 relaxin demonstrates antifibrotic properties via the RXFP1 receptor
MA Hossain, B Chow Suet Man, C Zhao, Q Xu, XJ Du, JD Wade, CS Samuel
Biochemistry | Published : 2011
DOI: 10.1021/bi1013968
Abstract
Human gene 3 (H3) relaxin is the most recently discovered member of the relaxin peptide family and can potentially bind all of the defined relaxin family peptide receptors (RXFP1-4). While its effects as a neuromodulator are being increasingly studied through its primary receptor, RXFP3, its actions via other RXFPs are poorly understood. Hence, we specifically determined the antifibrotic effects and mechanisms of action of H3 relaxin via the RXFP1 receptor using primary rat ventricular fibroblasts in vitro, which naturally express RXFP1, but not RXFP3, and a mouse model of fibrotic cardiomyopathy in vivo. Transforming growth factor β1 (TGF-β1) administration to ventricular fibroblasts signif..
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Awarded by NHMRC
Funding Acknowledgements
This study was supported by a John T. Reid Charitable Trusts Fellowship to M.A.H., National Health and Medical Research Council (NHMRC) of Australia Senior Research Fellowships to X.-J.D. and J.D.W., a National Heart Foundation of Australia/NHMRC RD Wright Fellowship to C.S.S., and a NHMRC Project Grant (508995) to J.D.W. and by the Victorian Government's Operational Infrastructure Support Program.