| Literature DB >> 30195439 |
Sanna Hagman1, Aliisa Mäkinen1, Laura Ylä-Outinen2, Heini Huhtala3, Irina Elovaara4, Susanna Narkilahti5.
Abstract
Multiple Sclerosis (MS) is an inflammatory neurodegenerative disease, where neural progenitor cell (NPC) transplantation has been suggested as a potential neuroprotective therapeutic strategy. Since the effect of inflammation on NPCs is poorly known, their effect on the survival and functionality of human NPCs were studied. Treatment with interleukin (IL)-6, tumor necrosis factor (TNF)-α and interferon (IFN)-γ did not induced cytotoxicity, but IFN-γ treatment showed decreased proliferation and neuronal migration. By contrast, increased proliferation and inhibition of electrical activity were detected after TNF-α treatment. Treatments induced secretion of inflammatory factors. Inflammatory cytokines appear to modulate proliferation as well as the cellular and functional properties of human NPCs.Entities:
Keywords: Cytokines; Human pluripotent stem cells; IFN-γ; IL-6; Microelectrode array; Multiple sclerosis; Neural cells; TNF-α
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Year: 2018 PMID: 30195439 DOI: 10.1016/j.jneuroim.2018.07.010
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478