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Topic: qPCR

ePoster
3 ePosters

In Neuroscience

Characterization of zebrafish larvae with knockouts in the NMDA receptor subunit genes grin2Aa and grin2Ab

Vera Abramova, Bohdan Kysilov, Ales Balik, Eni Tomovic, Tereza Smejkalova, Miloslav Korinek, Klevinda Fili, Mark Dobrovolskii, Paulina Bozikova, Jiri Cerny, Ladislav Vyklicky · FENS Forum 2024

Danio rerio (zebrafish) is a model for studying neurophysiological development and gene mutation consequences. Zebrafish possesses orthologs of human NMDA receptor subunit genes, including grin2Aa and grin2Ab for GRIN2A. The grin2Ab knockout strain created via CRISPR-Cas9, and the grin2Aa knockout were investigated for spatial and temporal gene expression and swimming behavior. Whole-mount in situ hybridization (WISH) was performed on wild-type (WT) zebrafish larvae aged 1, 3, and 5 days post fertilization (dpf). The results indicated minimal expression of both genes at 1 dpf. By 3 dpf, grin2A

ePoster · Neuroscience

MicroRNA-34a from GABAergic neurons of the raphe contributes to its peripheral plasma level

Elena Tittarelli, Serafina Manila Guzzo, Donald Ielpo, Elena Fiori, Carlo Cifani, Rossella Ventura, Diego Andolina, Luisa Lo Iacono · FENS Forum 2024

Aims: The identification of peripheral biomarkers of brain dysfunctions is essential to aid diagnosis and facilitate patient stratification. MicroRNAs are excellent candidate molecules to this purpose, as they can be expressed in the brain with regional and functional specificity, and they are highly stable in blood serum, unlike other RNA transcripts. Mir-34a is expressed with high specificity in a subpopulation of GABAergic neurons within the mouse Dorsal Raphe Nuclei (DRN), where it regulates GABAergic transmission in response to aversive stimuli. However, a direct connection between the br

ePoster · Neuroscience

SH-SY5Y cell differentiation to dopaminergic neuron-like cells using retinoic acid

Simas Janutenas, Vassileios Stratoulias, Umamaheswari Umasankar, Silvia Orsini · FENS Forum 2024

Background: We study dopaminergic neurons with specific emphasis on Parkinson’s disease. Our work involves implementing procedures for examining in vitro mouse primary dopaminergic neurons as well as dopaminergic neurons derived from human stem cells. Here we want to establish a continuous cell line model for fast and cost-effective production of human dopaminergic-like cells to be used in our studies. Aims: Differentiate SH-SY5Y cells into dopaminergic-like cells using Retinoic Acid. Optimize the differentiation protocol for highest yield of TH positive cells. Methods: Retinoic Acid is used t

ePoster · Neuroscience