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- W4308256424 endingPage "540" @default.
- W4308256424 startingPage "524" @default.
- W4308256424 abstract "Genomic analyses have revealed heterogeneity among glial progenitor cells (GPCs), but the compartment selectivity of human GPCs (hGPCs) is unclear. Here, we asked if GPCs of human grey and white brain matter are distinct in their architecture and associated gene expression. RNA profiling of NG2-defined hGPCs derived from adult human neocortex and white matter differed in their expression of genes involved in Wnt, NOTCH, BMP and TGFβ signaling, suggesting compartment-selective biases in fate and self-renewal. White matter hGPCs over-expressed the BMP antagonists BAMBI and CHRDL1, suggesting their tonic suppression of astrocytic fate relative to cortical hGPCs, whose relative enrichment of cytoskeletal genes presaged their greater morphological complexity. In human glial chimeric mice, cortical hGPCs assumed larger and more complex morphologies than white matter hGPCs, and both were more complex than their mouse counterparts. These findings suggest that human grey and white matter GPCs comprise context-specific pools with distinct functional biases." @default.
- W4308256424 created "2022-11-09" @default.
- W4308256424 creator A5016046874 @default.
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- W4308256424 creator A5032967943 @default.
- W4308256424 creator A5032969395 @default.
- W4308256424 creator A5035080848 @default.
- W4308256424 creator A5056977272 @default.
- W4308256424 date "2022-11-05" @default.
- W4308256424 modified "2023-10-17" @default.
- W4308256424 title "Glial progenitor cells of the adult human white and grey matter are contextually distinct" @default.
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