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• W1804594775 abstract "The complement system has been implicated in the removal of dysfunctional synapses and neurites during development and in disease processes in the mouse, but it is unclear how far the mouse data can be transferred to humans. Here, we co-cultured macrophages derived from human THP1 monocytes and neurons derived from human induced pluripotent stem cells, to study the role of the complement system in a human model. Components of the complement system were expressed by the human macrophages and human neuronal culture, while receptors of the complement cascade were expressed by human macrophages as shown via gene transcript analysis and flow cytometry. We mimicked pathological conditions leading to an altered glycocalyx by treatment of human neurons with sialidases. Desialylated human neurites were opsonized by the complement component C1q. Furthermore, human neurites with an intact sialic acid cap remained untouched, while desialylated human neurites were removed and ingested by human macrophages. While blockage of the complement receptor 1 (CD35) had no effect, blockage of CD11b as part of the complement receptor 3 (CR3) reversed the effect on macrophage phagocytosis of desialylated human neurites. Data demonstrate that in the human system sialylation of the neuronal glycocalyx serves as an inhibitory flag for complement binding and CR3-mediated phagocytosis by macrophages. GLIA 2016;64:35–47" @default.
• W1804594775 created "2016-06-24" @default.
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• W1804594775 date "2015-08-10" @default.
• W1804594775 modified "2023-10-17" @default.
• W1804594775 title "Sialylation of neurites inhibits complement-mediated macrophage removal in a human macrophage-neuron Co-Culture System" @default.
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• W1804594775 doi "https://doi.org/10.1002/glia.22901" @default.
• W1804594775 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4715670" @default.
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• W1804594775 hasPublicationYear "2015" @default.
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