mProX™ Human HTR2A Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- GPCR Cell Lines
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Published Data
Fig.1 The enhanced expression of inflammatory genes and lipogenesis were both influenced by the HTR2A/PPARg2 signaling pathway.
Pparg, Pparg1, and Pparg2 messenger RNA (mRNA) expression in the liver of SD rats. The liver of SD rats expressed Fas mRNA. PPARg2 protein expression in SD rats' liver and BRL-3A cells. Plin2 and Cd36's mRNA expression in BRL-3A.
Ref: Wang, Lulu, et al. "Gut-derived serotonin contributes to the progression of non-alcoholic steatohepatitis via the liver HTR2A/PPARγ2 pathway." Frontiers in Pharmacology 11 (2020): 553.
Pubmed: 32477107
DOI: 10.3389/fphar.2020.00553
Research Highlights
Serotonin 2A receptor remains a key pharmacological target for psychiatric, neurological, and cardiovascular diseases despite being heavily implicated in genetic association research. The architecture of the serotonin 2A receptor gene (HTR2A) was redefined by RNA sequencing, which also revealed novel mRNA transcript isoforms that made use of the gene's untranslated regions.
Ruble, Cara L., et al. "Genomic structure and expression of the human serotonin 2A receptor gene (HTR2A) locus: identification of novel HTR2A and antisense (HTR2A-AS1) exons." BMC genetics 17 (2016): 1-15.
Pubmed:
26738766
DOI:
10.1186/s12863-015-0325-6
The current study confirmed the association between HTR2A mutations and MDD treatment responsiveness to antidepressants, but not MDD susceptibility.
Kao, Chung-Feng, et al. "Gene-based association analysis suggests association of htr2a with antidepressant treatment response in depressed patients." Frontiers in Pharmacology 11 (2020): 1762.
Pubmed:
33519430
DOI:
10.3389/fphar.2020.559601