mProX™ Human GNRHR Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- GPCR Cell Lines
To download a Certificate of Analysis, please enter a lot number in the search box below. Note: Certificate of Analysis not available for kit components.
Lot Number
Made to Order Inquiry
InquiryProduct Information
Product Properties
Protocols
Please visit our protocols page.
Customer Reviews
There are currently no Customer reviews or questions for mProX™ Human GNRHR Stable Cell Line (S01YF-0923-PY86). Click the button above to contact us or submit your feedback about this product.
Paul (Verified Customer)
Patrick Liam (Creative Biolabs Scientific Support)
Paul (Verified Customer)
Patrick Liam (Creative Biolabs Scientific Support)
Published Data
Fig.1 An in-depth exploration of the p.Thr269Met GNRHR mutation's impact on hypogonadotropic hypogonadism, unraveling its functional intricacies.
COS-7 cells underwent transfection with either the wild-type (WT) or the p.Thr269Met mutant GnRHR, followed by GnRH stimulation for one hour, featuring incremental concentrations (ranging from 10^-10 to 10^-7 M) of a synthetic GnRH ligand [log M]. Intracellular inositol phosphate (IP) accumulation was quantified in triplicates of lysed cells utilizing the IP3 Elisa kit at 450 nm. A notably diminished dose-response induction of IP accumulation was observed in comparison to WT GNRHR-transfected cells, consistently registering lower levels than those elicited by WT-GNRHR transfection. These findings were graphed on GraphPad Prism relative to the maximum response of a standard IP curve, revealing statistical significance (*, p < 0.05) denoting reduced IP accumulation in the p.Thr269Met mutant compared to the WT GnRHR.
Ref: Correa-Silva, Silvia Regina, et al. "A novel GNRHR gene mutation causing congenital hypogonadotrophic hypogonadism in a Brazilian kindred." Journal of Neuroendocrinology 30.12 (2018): e12658.
Pubmed: 30415482
DOI: 10.1111/jne.12658
Research Highlights
Santos LC, et al. "Kisspeptin treatment reverses high prolactin levels and improves gonadal function ." Scientific reports, 2023.
The effects of kisspeptin-10 (Kp10) administration on restoring gonadal function in hypothyroid male rats were evaluated in this study. Hypothyroidism was induced using 6-propyl-2-thiouracil (PTU) for three months, after which half of the hypothyroid rats were treated with Kp10 in the last month. Results showed that hypothyroidism decreased testicular and sex gland mass, as well as sperm morphology, motility, and vigor. It also reduced Kiss1 and Kiss1r protein and gene expression and affected various hormone levels in the pituitary and hypothalamus. Treatment with Kp10 showed improvements in testicular and seminal vesicle morphology, sperm quality, hormone levels, and gene expression in the testis, pituitary, and hypothalamus in hypothyroid rats. These findings suggest that Kp10 treatment can reverse the inhibitory effects of hypothyroidism on the male gonadal axis and improve sperm quality.
Pubmed:
37798396
DOI:
10.1038/s41598-023-44056-z
Olea GB, et al. "Early gonadogenesis in Columba livia (Birds: Columbiformes): migration, ." Development, growth & differentiation, 2023.
In avian species, the process of migration and colonization of primordial germ cells (PGCs) in the gonadal crest is carried out through the bloodstream. Previous studies have used DDX4, SSEA1, and Oct4 to identify PGCs, while other molecules such as N-cadherin, GnRHR, and 3betaHSD have been used during gonadal development in mice and birds. However, their role in early gonadogenesis in birds is still poorly understood. This study aims to analyze the differential immunodetection of N-cadherin, Oct4, GnRHR, and 3betaHSD in Columba livia embryos during the migration and colonization of PGCs in the genital crest and early gonadogenesis stages. Immunohistochemistry was performed in corresponding histological sections of C. livia from stages (S) 15 to S40. The results showed that N-cadherin, Oct4, GnRHR, and 3betaHSD were immunodetected in the germ line of C. livia and were useful markers for identifying PGCs during their migration and colonization in the genital crest, as well as in early gonadogenesis. This study presents an effective model for understanding early gonadogenesis in altricial species and highlights the potential of these markers for future research.
Pubmed:
37795634
DOI:
10.1111/dgd.12895