| Literature DB >> 33482100 |
Sissel Ida Schmidt1, Helle Bogetofte1, Louise Ritter1, Jette Bach Agergaard1, Ditte Hammerich1, Amina Arslanagic Kabiljagic1, Agnieszka Wlodarczyk1, Silvia Garcia Lopez2, Mia Dahl Sørensen3, Mie Lærkegård Jørgensen1, Justyna Okarmus1, Alberto Martínez Serrano2, Bjarne Winther Kristensen4, Kristine Freude5, Trevor Owens6, Morten Meyer7.
Abstract
Microglia have recently been established as key regulators of brain development. However, their role in neuronal subtype specification remains largely unknown. Using three different co-culture setups, we show that microglia-secreted factors enhance dopaminergic differentiation of somatic and induced pluripotent stem cell-derived human neural stem cells (NSCs). The effect was consistent across different NSC and microglial cell lines and was independent of prior microglial activation, although restricted to microglia of embryonic origin. We provide evidence that the effect is mediated through reduced cell proliferation and decreased apoptosis and necrosis orchestrated in a sequential manner during the differentiation process. tumor necrosis factor alpha, interleukin-1β, and insulinlike growth factor 1 are identified as key mediators of the effect and shown to directly increase dopaminergic differentiation of human NSCs. These findings demonstrate a positive effect of microglia on dopaminergic neurogenesis and may provide new insights into inductive and protective factors that can stimulate in vitro derivation of dopaminergic neurons.Entities:
Keywords: IGF1; IL-1β; NSCs; Parkinson’s disease; TNFα; co-culture; dopamine; microglia; neuron-microglia interaction; secretome analysis
Year: 2021 PMID: 33482100 PMCID: PMC7878834 DOI: 10.1016/j.stemcr.2020.12.011
Source DB: PubMed Journal: Stem Cell Reports ISSN: 2213-6711 Impact factor: 7.765