NeuroToxicology, volume 105, pages 10-20

In vitro Cytotoxicity Assessment of Ruxolitinib on Oligodendrocyte Precursor Cell and Neural Stem/Progenitor Cell Populations

Cheng-Wei Lim 1
Ryo Ohtomo 2
A.C. Liang 2
Su Jing Chan 2
King-Hwa Ling 3, 4
Eng H. Lo 2
Ken ARAI 2
Pike-See Cheah 1, 2, 4
Publication typeJournal Article
Publication date2024-12-01
Journal: NeuroToxicology
scimago Q2
SJR0.829
CiteScore6.8
Impact factor3.4
ISSN0161813X, 18729711
Abstract
JAK-STAT signaling cascade has emerged as an ideal target for the treatment of myeloproliferative diseases, autoimmune diseases, and neurological disorders. Ruxolitinib (Rux), is an orally bioavailable, potent and selective Janus-associated kinase (JAK) inhibitor, proven to be effective to target activated JAK-STAT pathway in the diseases previously described. Unfortunately, limited studies have investigated the potential cytotoxic profile of Rux on other cell populations within the heterogenous CNS microenvironment. Two stem and progenitor cell populations, namely the oligodendrocyte precursor cells (OPCs) and neural stem/progenitor cells (NSPCs), are important for long-term maintenance and post-injury recovery response of the CNS. In light of the limited evidence, this study sought to investigate further the effect of Rux on proliferating and differentiating OPCs and NSPCs populations. In the present study, cultured rat OPCs and NSPCs were treated with various concentrations of Rux, ranging from 2 μM to 20 μM. The effect of Rux on proliferating OPCs (PDGF-R-α

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