mProX™ Human HTR5A Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- GPCR Cell Lines
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Published Data
Fig.1 Dose-response split TEV assay for the serotonin receptor HTR5A using the agonist serotonin.
Increasing serotonin concentrations triggered the HTR5A serotonin receptor. Serotonin concentration of 160 nM was used to get the EC 50 value (gray lines). Transient fusions of HTR5A-V2R-NTEV-tevS-GV and ARRB2-CTEV were observed.
Ref: Wehr, Michael C., Sabrina Galinski, and Moritz J. Rossner. "Monitoring G protein-coupled receptor activation using the protein fragment complementation technique split TEV." G Protein-Coupled Receptor Screening Assays: Methods and Protocols (2015): 107-118.
Pubmed: 25563180
DOI: 10.1007/978-1-4939-2336-6_8
Research Highlights
Two serotonin (S) receptors, HTR2c and HTR5a, were shown to be expressed and functionally up-regulated by cortisol, according to the analysis. When pre-adipocytes were cultured alone or with macrophages present, HTR2c and HTR5a were also directly implicated in mediating cortisol accelerated adipogenesis.
Priyadarshini, Sushri, et al. "Cortisol regulates immune and metabolic processes in murine adipocytes and macrophages through HTR2c and HTR5a serotonin receptors." European Journal of Cell Biology 97.7 (2018): 483-492.
Pubmed:
30097291
DOI:
10.1016/j.ejcb.2018.07.004
This study discovered that by boosting innate immune signals, valerenic acid can prevent GBM cells from proliferating, migrating, and invading. Valerenic Acid-induced cell death might be prevented by N-acetylcysteine's (NAC) inhibition of ROS or Compound C's attenuation of AMPK.
Lu, Qingli, Yuan Ding, and Yang Li. "5-HT receptor agonist Valerenic Acid enhances the innate immunity signal and suppresses glioblastoma cell growth and invasion." International Journal of Biological Sciences 16.12 (2020): 2104.
Pubmed:
32549758
DOI:
10.7150/ijbs.44906