Differentiation of two human neuroblastoma cell lines alters SV2 expression patterns

作者: Helgi B. Schiöth , Helgi B. Schiöth , Robert Fredriksson , Emilia Lekholm , Mikaela M. Ceder

DOI: 10.1186/S11658-020-00243-8

关键词:

摘要: The synaptic vesicle glycoprotein 2 (SV2) family is essential to the machinery involved in neurotransmission and recycling. isoforms SV2A, SV2B SV2C are implicated neurological diseases such as epilepsy, Alzheimer’s Parkinson’s disease. Suitable cell systems for studying regulation of these proteins essential. Here we present gene expression data two human neuroblastoma lines after differentiation. Human SiMa IMR-32 were treated seven days with growth supplements (B-27 N-2), all-trans-retinoic acid (ATRA) or vasoactive intestinal peptide (VIP) levels SV2 neuronal targets analyzed. reacted differently treatments, only one three was affected at a time. choline O-acetyltransferase (CHAT) changed concert supplement treatment, decreasing cells while increasing IMR-32. ATRA treatment resulted no detected changes either line VIP increased both dopamine transporter (DAT) cells. synergistic patterns between CHAT well DAT mirror connectivity found disease models knock-out animals, although here genetic alteration made. These differentiation treatments could possibly be used study function.

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