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. 2019 Nov 21;13(6):1022–1037. doi: 10.1016/j.stemcr.2019.10.012

Figure 2.

Figure 2

Differentiation of Grafted Human iNPCs in Hippocampus of Immunodeficient Mice

(A) Total numbers of KU80+ human cells in the hippocampus of immunodeficient mice 2, 4, 6, and 12 months post transplantation (M p.t.).

(B) The coronal brain section harboring grafted GFP+ human iNPCs at 2, 4, 6, and 12 M p.t. (Top) Immunofluorescence analysis of KU80 expression among GFP+ cells (second panel). Cell nuclei were counterstained with DAPI.

(C) Immunofluorescence analysis of NEUN and GFAP expression in KU80+ cells. The dashed line indicates the KU80NEUN+ host neurons mixing with grafted cells.

(D) Percentages of NEUN+ mature neurons and GFAP+ astrocytes among KU80+ grafted human cells shown in (C).

(E) Immunofluorescence analysis of subtypes of human iNPC-derived neurons among KU80+ cells at 4 M p.t.

(F) Quantification of the results shown in (E).

(G) Percentages of Ki67+ cells among KU80+ grafted cells at 1, 2, 4, 6, and 12 M p.t. shown in Figure S3D.

Scale bars, 500 μm (B), 50 μm (magnified image in B) and 25 μm (C and E). n = 3 mice per time point. Data are represented as scatterplots with mean ± SD. Related to Figure S3.