Microglia are increasingly implicated in brain pathology, particularly neurodegenerative disease, with many genes implicated in Alzheimer's, Parkinson's, and motor neuron disease expressed in microglia. There is, therefore, a need for authentic, efficient in vitro models to study human microglial pathological mechanisms. Microglia originate from the yolk sac as MYB-independent macrophages, migrating into the developing brain to complete differentiation. Here, we recapitulate microglial ontogeny by highly efficient differentiation of embryonic MYB-independent iPSC-derived macrophages then co-culture them with iPSC-derived cortical neurons. Co-cultures retain neuronal maturity and functionality for many weeks. Co-culture microglia express key microglia-specific markers and neurodegenerative disease-relevant genes, develop highly dynamic ramifications, and are phagocytic. Upon activation they become more ameboid, releasing multiple microglia-relevant cytokines. Importantly, co-culture microglia downregulate pathogen-response pathways, upregulate homeostatic function pathways, and promote a more anti-inflammatory and pro-remodeling cytokine response than corresponding monocultures, demonstrating that co-cultures are preferable for modeling authentic microglial physiology.
Stem cell reports
1727 - 1742
Alzheimer's disease, Parkinson's disease, cortical neurons, human, iPSC, induced pluripotent stem cell, macrophage, microglia, neurodegeneration, neuroinflammation, Cells, Cultured, Coculture Techniques, Cytokines, Down-Regulation, Humans, Macrophages, Microglia, Models, Biological, Neurodegenerative Diseases, Neurons, Phagocytosis, Pluripotent Stem Cells, Proto-Oncogene Proteins c-myb, Transcriptome, fms-Like Tyrosine Kinase 3