Value Added Abstracts
Emiliano Tesoro-Cruz
Abstract
Tryptophan hydroxylase-type 2 (Tph2) is the first, rate- limiting step in the biosynthesis of serotonin (5-HT) in the brain. The ophthalmic-administration (Op-Ad) is a non- invasive method that allows delivering genetic vehicles through the eye and reach the brain. In this work, the murine Tph-2 gene was cloned in a non-viral vector (pIRES-hrGFP- 1a), generating pIRES-hrGFP-1a-Tph2, plus the Tag- FLAG. Recombinant Tph2-FLAG was detected and tested in vitro and in vivo, where 25μg of pIRES-hrGFP-1a-Tph2- FLAG was Op-Ad to mice. The construct was capable of expressing and producing the recombinant Tph2-FLAG. Assays in vivo showed that the construct efficiently crossed the Hemato-Ocular-Barrier and the Blood-Brain-Barrier, reaching brain cells, passed the optical nerves, and transcribed mRNA-Tph2-FLAG in different brain areas. The recombinant Tph2-FLAG was observed in amygdala and brainstem, mainly in raphe dorsal and medial. Relative Tph2 expression of three-fold over basal level was recorded three days after Op-Ad. Besides, we have evidence that recombinant Tph2-FLAG was functional during the 5-HT biosynthesis; this was observed in vitro and in vivo. The 5HT levels were increased in HEK293 cells transfected (6.02ng/mL) vs control (2.87ng/mL) at 48 h after transfection. Moreover, in mice showed an increase with respect to the control: in the amygdala (325ng/mL//125ng/mL) and in the hypothalamus (104ng/mL//68ng/mL), respectively. These results demonstrated that IRES-hrGFP-Tph2-FLAG, administrated through the eyes was capable of reaching the brain, transcribing, and translating an exogenous Tph2 gene. In consequence the 5HT was increased in amygdala and hypothalamus at seven days after treatment. In conclusion, this study showed the feasibility of delivering therapeutic genes, such as the Tph2, the first enzyme, rate- limiting step in the 5-HT biosynthesis. Besides, these results support the possibility to use this innovative idea with therapeutic purposes and could be a strategy for those patients that possess risk TPH2 SNPs associated with depression disorder, and suicidality.