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Human Somatostatin SST(4) Receptor Transgenic Mice: Construction and Brain Expression Pattern Characterization

Somatostatin receptor subtype 4 (SST(4)) has been shown to mediate analgesic, antidepressant and anti-inflammatory functions without endocrine actions; therefore, it is proposed to be a novel target for drug development. To overcome the species differences of SST(4) receptor expression and function...

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Detalles Bibliográficos
Autores principales: Nemes, Balázs, Bölcskei, Kata, Kecskés, Angéla, Kormos, Viktória, Gaszner, Balázs, Aczél, Timea, Hegedüs, Dániel, Pintér, Erika, Helyes, Zsuzsanna, Sándor, Zoltán
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8038480/
https://www.ncbi.nlm.nih.gov/pubmed/33916620
http://dx.doi.org/10.3390/ijms22073758
Descripción
Sumario:Somatostatin receptor subtype 4 (SST(4)) has been shown to mediate analgesic, antidepressant and anti-inflammatory functions without endocrine actions; therefore, it is proposed to be a novel target for drug development. To overcome the species differences of SST(4) receptor expression and function between humans and mice, we generated an SST(4) humanized mouse line to serve as a translational animal model for preclinical research. A transposon vector containing the hSSTR4 and reporter gene construct driven by the hSSTR4 regulatory elements were created. The vector was randomly inserted in Sstr4-deficient mice. hSSTR4 expression was detected by bioluminescent in vivo imaging of the luciferase reporter predominantly in the brain. RT-qPCR confirmed the expression of the human gene in the brain and various peripheral tissues consistent with the in vivo imaging. RNAscope in situ hybridization revealed the presence of hSSTR4 transcripts in glutamatergic excitatory neurons in the CA1 and CA2 regions of the hippocampus; in the GABAergic interneurons in the granular layer of the olfactory bulb and in both types of neurons in the primary somatosensory cortex, piriform cortex, prelimbic cortex and amygdala. This novel SST(4) humanized mouse line might enable us to investigate the differences of human and mouse SST(4) receptor expression and function and assess the effects of SST(4) receptor agonist drug candidates.