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. 2018 Dec 27;12(1):6–13. doi: 10.1016/j.stemcr.2018.11.022

Figure 3.

Figure 3

Cxcr4 Knockdown Results in Lineage Progression and a Shift Away from the Vasculature

(A) CXCR4 expression in FACS-sorted lineage cells from the V-SVZ. ∗∗p < 0.01, ∗∗∗p < 0.001.

(B) Percentage of EdU + TdTomato cells in V-SVZ whole mounts at 7, 21, and 35 days after tamoxifen injection (n = 4–5 mice/group; ∗∗p < 0.01 by two-way analysis of variance).

(C) Confocal images of whole mounts immunostained for laminin to label vasculature and EdU to label actively proliferating cells at 7 and 35 days after recombination. Scale bar, 100 μm.

(D) Percentage of MASH1+ TdTomato cells in V-SVZ whole mounts at 7, 21, and 35 days after tamoxifen injection (n = 3–5 mice/group; ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001 by two-way analysis of variance).

(E) Numbers of TdTomato-positive neuroblasts did not significantly differ at any time point measured.

(F) Cxcr4 deletion significantly shifted distance of MASH1 relative to the vasculature (n = 3,642 cells across 4 Cxcr4+/+ mice, n = 3,166 cells across 3 Cxcr4fl/fl mice; p < 0.001 by Mann-Whitney test).

See also Figure S2.