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Microglia-Secreted Factors Enhance Dopaminergic Differentiation of Tissue- and iPSC-Derived Human Neural Stem Cells.
- Source :
-
Stem cell reports [Stem Cell Reports] 2021 Feb 09; Vol. 16 (2), pp. 281-294. Date of Electronic Publication: 2021 Jan 21. - Publication Year :
- 2021
-
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.<br /> (Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Apoptosis
Cell Line
Cells, Cultured
Coculture Techniques methods
Dopamine metabolism
Humans
Insulin-Like Growth Factor I metabolism
Interleukin-1beta metabolism
Mice
Mice, Inbred C57BL
Neurogenesis
Tumor Necrosis Factor-alpha metabolism
Cell Differentiation
Cell Proliferation
Cytokines metabolism
Dopaminergic Neurons metabolism
Induced Pluripotent Stem Cells physiology
Microglia physiology
Neural Stem Cells metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2213-6711
- Volume :
- 16
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Stem cell reports
- Publication Type :
- Academic Journal
- Accession number :
- 33482100
- Full Text :
- https://doi.org/10.1016/j.stemcr.2020.12.011