JPET

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on September 14, 2004; DOI: 10.1124/jpet.104.073486


0022-3565/05/3121-83-95$20.00
JPET 312:83-95, 2005
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
jpet.104.073486v1
312/1/83    most recent
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Chen, J.
Right arrow Articles by Liu, C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chen, J.
Right arrow Articles by Liu, C.

CELLULAR AND MOLECULAR

Pharmacological Characterization of Relaxin-3/INSL7 Receptors GPCR135 and GPCR142 from Different Mammalian Species

Jingcai Chen, Chester Kuei, Steven W. Sutton, Pascal Bonaventure, Diane Nepomuceno, Elo Eriste, Rannar Sillard, Timothy W. Lovenberg, and Changlu Liu

Johnson & Johnson Pharmaceutical Research and Development, L.L.C., San Diego, California (J.C., C.K., S.W.S., P.B., D.N., T.W.L., C.L.); and Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden (E.E., R.S.)

Relaxin-3 has recently been identified as a ligand for two structurally related G-protein-coupled receptors, human GPCR135 and GPCR142. This current study reports the characterization of mouse and rat GPCR135 as well as GPCR142 from mouse, monkey, cow, and pig at the molecular and pharmacological levels. Mouse and rat GPCR135 exhibit high homology (>85%) to the human GPCR135 and have very similar pharmacological properties to that of the human GPCR135. Human and mouse/rat relaxin-3 both bind to and activate mouse, rat, and human GPCR135 at high affinity with IC50 or EC50 values close to 0.5 nM. In contrast, the mouse GPCR142 is less well conserved (74% homology) with human GPCR142. The rat GPCR142 gene was found to be a pseudogene. We further cloned GPCR142 genes from monkey, cow, and pig and found that they are highly homologous (>84%) to human GPCR142. Pharmacological characterization of GPCR142 from different species demonstrated that relaxin-3 binds to GPCR142 from different species at high affinity (IC50 < 5 nM). However, relaxin-3 does not stimulate a Ca2+ response in cells coexpressing G{alpha}16 and mouse GPCR142, whereas it does for cells expressing GPCR142 from other species tested. Our results suggest that GPCR142 may have a diminished role as a receptor for relaxin-3 in rodents, or perhaps GPCR142 functions as a receptor for another ligand in nonrodents. Boels and Schaller recently reported bradykinin as a ligand for GPCR142 (also known as GPR100). In this report, we demonstrate that bradykinin activates neither GPCR135 nor GPCR142, whereas relaxin-3 does.


Received for publication June 30, 2004
Accepted September 14, 2004.

Address correspondence to: Dr. Changlu Liu, Johnson & Johnson Pharmaceutical Research and Development, L.L.C., 3210 Merryfield Row, San Diego, CA 92121. E-mail: cliu9{at}prdus.jnj.com




This article has been cited by other articles:


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
B. M. McGowan, S. A. Stanley, J. Donovan, E. L. Thompson, M. Patterson, N. M. Semjonous, J. V. Gardiner, K. G. Murphy, M. A. Ghatei, and S. R. Bloom
Relaxin-3 stimulates the hypothalamic-pituitary-gonadal axis
Am J Physiol Endocrinol Metab, August 1, 2008; 295(2): E278 - E286.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
C. Kuei, S. Sutton, P. Bonaventure, C. Pudiak, J. Shelton, J. Zhu, D. Nepomuceno, J. Wu, J. Chen, F. Kamme, et al.
R3(B{Delta}23 27)R/I5 Chimeric Peptide, a Selective Antagonist for GPCR135 and GPCR142 over Relaxin Receptor LGR7: IN VITRO AND IN VIVO CHARACTERIZATION
J. Biol. Chem., August 31, 2007; 282(35): 25425 - 25435.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
B. M. McGowan, S. A. Stanley, N. E. White, A. Spangeus, M. Patterson, E. L. Thompson, K. L. Smith, J. Donovan, J. V. Gardiner, M. A. Ghatei, et al.
Hypothalamic mapping of orexigenic action and Fos-like immunoreactivity following relaxin-3 administration in male Wistar rats
Am J Physiol Endocrinol Metab, March 1, 2007; 292(3): E913 - E919.
[Abstract] [Full Text] [PDF]


Home page
FASEB J.Home page
J. Novak, L. J. Parry, J. E. Matthews, L. J. Kerchner, K. Indovina, K. Hanley-Yanez, K. D. Doty, D. O. Debrah, S. G. Shroff, and K. P. Conrad
Evidence for local relaxin ligand-receptor expression and function in arteries
FASEB J, November 1, 2006; 20(13): 2352 - 2362.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
J. D. Silvertown, J. S. Walia, A. J. Summerlee, and J. A. Medin
Functional Expression of Mouse Relaxin and Mouse Relaxin-3 in the Lung from an Ebola Virus Glycoprotein-Pseudotyped Lentivirus via Tracheal Delivery
Endocrinology, August 1, 2006; 147(8): 3797 - 3808.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
B. M. C. McGowan, S. A. Stanley, K. L. Smith, N. E. White, M. M. Connolly, E. L. Thompson, J. V. Gardiner, K. G. Murphy, M. A. Ghatei, and S. R. Bloom
Central Relaxin-3 Administration Causes Hyperphagia in Male Wistar Rats
Endocrinology, August 1, 2005; 146(8): 3295 - 3300.
[Abstract] [Full Text] [PDF]


Home page
Mol. Pharmacol.Home page
C. Liu, J. Chen, C. Kuei, S. Sutton, D. Nepomuceno, P. Bonaventure, and T. W. Lovenberg
Relaxin-3/Insulin-Like Peptide 5 Chimeric Peptide, a Selective Ligand for G Protein-Coupled Receptor (GPCR)135 and GPCR142 over Leucine-Rich Repeat-Containing G Protein-Coupled Receptor 7
Mol. Pharmacol., January 1, 2005; 67(1): 231 - 240.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 2005 by the American Society for Pharmacology and Experimental Therapeutics.