Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2005 Apr;31(2-3):153-6.
doi: 10.1007/s10695-006-0018-1.

GnRH and gpcr: laser-captured single cell gene profiling

Affiliations

GnRH and gpcr: laser-captured single cell gene profiling

Ishwar S Parhar. Fish Physiol Biochem. 2005 Apr.

Abstract

We have developed a novel single cell real-time quantitative PCR technique, which incorporates harvesting marker-identified single cells using laser-capture. Here, for the first time in a vertebrate species, using this innovative single cell gene profiling technique, we report the presence of G-protein coupled receptors in individual gonadotropin-releasing hormone (GnRH) neurons and endocrine cells of the pituitary of the tilapia Oreochromis niloticus. The differential expression of multiple combinations of three GnRH receptor types (R1, R2 and R3) in individual gonadotropic and nongonadotropic cells demonstrates cellular and functional heterogeneity. The differential use of GnRH receptors in corticotropes, melanotropes and thyrotropes during gonadal maturation and reproductive behaviors suggests new roles for these hormones. Further, we provide evidence of the structure of a novel nonmammalian G-protein coupled receptor (GPR54) for kisspeptins, encoded by Kiss-1 gene, which is highly conserved during evolution and expressed in GnRH1, GnRH2 and GnRH3 neurons. We hypothesize GPR54 stimulates GnRH secretion and is crucial for pubertal maturation. We speculate, the use of this method will allow the identification and quantification of known and unknown genes in single cells, which would greatly facilitate our understanding of the complex interactions that govern the physiology of individual cells in vertebrates species.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Trends Endocrinol Metab. 2003 Jan;14(1):35-43 - PubMed
    1. Proc Natl Acad Sci U S A. 2005 Feb 1;102(5):1761-6 - PubMed
    1. Endocr Rev. 2004 Apr;25(2):235-75 - PubMed
    1. Endocrinology. 2001 Nov;142(11):4729-39 - PubMed
    1. Gen Comp Endocrinol. 2004 Jan 1;135(1):1-16 - PubMed