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. Author manuscript; available in PMC: 2021 Aug 5.
Published in final edited form as: Neuron. 2020 Jun 1;107(3):436–453.e12. doi: 10.1016/j.neuron.2020.05.014

Figure 8: Maturation state affects CD49f+ hiPSC-derived astrocytes response to stimulation with TNFα, IL1α, and C1q.

Figure 8:

See also Supplemental Table 1.

a) tSNE plots of single-cell RNA-Seq data from unstimulated (A0, n = 5,881) and TNFα, IL-1α, and C1q stimulated (A1, n = 6,701) astrocytes, shown by cluster (left) and by treatment type (right). Data from two iPSC lines (lines 1 and 3, n = 2).

b) Quantification of cell type proportions from unstimulated (A0) and A1 astrocytes.

c) Dot plot of pan, A1-specific, and A2-specific astrocyte transcripts in A0 (blue) and A1 astrocytes (red), highlighting a stronger gene expression response in mature astrocytes. Dot size represents the percentage of cells that express a transcript, and color intensity represents the expression level of a transcript.

d) tSNE feature plots of reactive astrocyte transcripts.

e) GFAP protein levels are stable in A0 and A1 CD49f+ hiPSC-astrocytes. Western blots for GFAP and b-actin, and quantification of protein levels, normalized to b-actin. Error bars show mean ± standard deviation (n=5, 1-2 replicates per line). Colored dots correspond to 3 different lines. p-values were calculated using a two-tailed, paired t-test.

f) TIMP1 level increases in CD49f+ hiPSC-astrocytes stimulated to A1. Western blots for TIMP1 and b-actin, and protein quantification, normalized to b-actin. Error bars show mean ± standard deviation (n=5, 1-2 replicates per line). Colored dots correspond to 3 different lines. p-values were calculated using a two-tailed, paired t-test.

Abbreviations: Imm.=immature; Trans.=transitioning.