We know of 4 glycoprotein hormones (LH, FSH, CG and TSH) and know that they interact with specific receptors that belong to the superfamily of the G protein-coupled receptors (GPCRs). The striking characteristic of the glycoprotein hormone receptors, when compared to other GPCRs, is that they contain a large leucine rich repeat-containing extracellular domain. Recently, five more GPCRs containing large leucine-repeat rich ectodomains have been cloned (LGR4-8). These GPCRs are sequentially-related to LH/FSH/TSH receptors but do not bind these hormones. They fall therefore into the class of the """"""""orphan"""""""" GPCRs, receptors awaiting to be matched to a ligand. We hypothesize that these receptors bind thus far undescribed protein hormones and propose to isolate and characterize these hormones. We have developed a strategy that allows us to discover the natural ligands of orphan GPCRs. In short, the orphan GPCR-induced second messenger response is used to monitor the identification and purification of this orphan GPCR ligand from tissue extracts. We have preliminary data that indicate that pituitary protein extracts at various stages of purification are able to elicit a reproducible second messenger response in cells transfected with LGR4. It has also recently been discovered, by sequence analysis, that the human genome encodes two proteins (alpha2 and beta10) that are different but structurally similar to the glycoprotein hormones. We propose first to test whether alpha2 and beta10 can activate any of the orphan LGRs. We propose also to complete the isolation of the natural ligand of LGR4 and determine its sequence and isolate and sequence the natural ligands of LGR5 and 6. We will then analyze these novel ligands for their pharmacological and biological activates in vitro. Finally, we will study their roles in vivo, in particular test whether they exert a hormonal function.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK063001-02
Application #
6729880
Study Section
Biochemical Endocrinology Study Section (BCE)
Program Officer
Malozowski, Saul N
Project Start
2003-04-01
Project End
2007-02-28
Budget Start
2004-03-01
Budget End
2005-02-28
Support Year
2
Fiscal Year
2004
Total Cost
$293,533
Indirect Cost
Name
University of California Irvine
Department
Pharmacology
Type
Schools of Medicine
DUNS #
046705849
City
Irvine
State
CA
Country
United States
Zip Code
92697
Zhang, Li; Parks, Gregory S; Wang, Zhiwei et al. (2013) Anatomical characterization of bombesin receptor subtype-3 mRNA expression in the rodent central nervous system. J Comp Neurol 521:1020-39
Garcia-Fuster, M J; Parks, G S; Clinton, S M et al. (2012) The melanin-concentrating hormone (MCH) system in an animal model of depression-like behavior. Eur Neuropsychopharmacol 22:607-13
Chung, Shinjae; Liao, Xiao-Hui; Di Cosmo, Caterina et al. (2012) Disruption of the melanin-concentrating hormone receptor 1 (MCH1R) affects thyroid function. Endocrinology 153:6145-54
Civelli, Olivier (2012) Orphan GPCRs and neuromodulation. Neuron 76:12-21
Zhang, Yan; Xu, Junyan; Wang, Zhiwei et al. (2012) BmK-YA, an enkephalin-like peptide in scorpion venom. PLoS One 7:e40417
Chung, Shinjae; Verheij, Michel M M; Hesseling, Peter et al. (2011) The melanin-concentrating hormone (MCH) system modulates behaviors associated with psychiatric disorders. PLoS One 6:e19286
Lee, Cheol; Parks, Gregory S; Civelli, Olivier (2011) Anxiolytic effects of the MCH1R antagonist TPI 1361-17. J Mol Neurosci 43:132-7
Parks, Gregory S; Okumura, Sean M; Gohil, Krupa et al. (2010) Mice lacking Melanin Concentrating Hormone 1 receptor are resistant to seizures. Neurosci Lett 484:104-7
Chung, Shinjae; Saito, Yumiko; Civelli, Olivier (2009) MCH receptors/gene structure-in vivo expression. Peptides 30:1985-9
Nagasaki, Hiroshi; Chung, Shinjae; Dooley, Colette T et al. (2009) The pharmacological properties of a novel MCH1 receptor antagonist isolated from combinatorial libraries. Eur J Pharmacol 602:194-202

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