Fig. 4From: Comparison of two protocols for the generation of iPSC-derived human astrocytesCharacterization of cell type composition. A. Heatmap displaying expression values for astrocytic and neuronal markers. B. Validation of GFAP, S100B, SLC1A3, and MAP2 expression profiles using qPCR. CTRL1, control 1; CTRL2, control 2. For each protocol and cell line, three biological replicates were used. Data are presented as the mean ± SD,*P ≤ 0.05, **P ≤ 0.01, ***P ≤ 0.001, ***P ≤ 0.0001. C. Heatmap showing the percentage of iPSC-derived cells in astrocytic cultures sharing the expression profile with the cell types identified in Smajic et al. [41]. D. Heatmap showing the percentage of generated astrocytic cultures sharing the expression signatures with the cortical cell types identified in Agarwal et al. [40]. E. Heatmap displaying the comparison of the generated astrocytes with the dataset from human embryonal midbrain at week 8 [42]. CTRL1, control 1; CTRL2, control 2; Mgl, microglia; Astro, astrocytes; Epend, ependymal cells; ODCs, oligodendrocytes; Neur, neurons; OPCs, oligodendrocyte precursor cells; ProgFPL, lateral floorplate progenitor; Rgl1, radial glia-like cell type 1; NbML1, mediolateral neuroblast type 1; OMTN, oculomotor and trochlear nucleus; DA1, dopaminergic neurons 1; NbML5, mediolateral neuroblast type 5; ProgM, midline neuronal progenitor; ProgFPM, medial floorplate progenitor; RN, red nucleus; DA0, dopaminergic neurons 0; NbM, medial neuroblasts; NProg, neuronal progenitor; ProgBP, basal plate progenitorBack to article page