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. Author manuscript; available in PMC: 2015 Nov 6.
Published in final edited form as: Cell Stem Cell. 2014 Oct 9;15(5):619–633. doi: 10.1016/j.stem.2014.09.009

Figure 2. BMP restricts the Shh-expressing IRS progenitor pool.

Figure 2

(A) Experimental timeline for selectively targeting Bmpr1a ablation in Shh-expressing TACs during full-anagen. (B–D) BMPR1a loss results in an expansion of YFP+ cKO TACs and an increase in their proliferation. (E) Lineage tracing of YFP+ TAC progeny. (F and G) Differential distribution of YFP+ progeny reveals an increase in AE15+ IRS and decrease in AE13+ cortex following Bmpr1a ablation in TACs. (H) Bmpr1a-null YFP+ TACs lineage trace to AE15+ IRS but not AE13+ cortex. (I) Axin2-LacZ activity in Shh-expressing TACs, DP and cortex/medulla. Note lack of X-Gal staining (blue) in HS developing from Bmpr1a-targeted side. (J) LEF1+ TACs are expanded upon BMPR1a loss, but LEF1+ cortex is absent. (K) Shh+ IRS TACs are expanded and express elevated Shh in the absence of BMP signaling. (L) GATA3+ cells are expanded following Bmpr1a ablation in Shh+ TACs. (M and N) Lineage tracing of YFP+ progeny following Gata3 ablation in Shh+ TACs. Following loss of GATA3, AE15+ IRS progeny (external to the K82+ HS cuticle) are lost, while AE15+ HS progeny (internal to K82) are expanded. (O) Gata3 ablation in Shh+ TACs leads to an expanded cortical layer (AE13+) and smaller AE15+ IRS. (P) EM of Gata3 straight KO HFs reveals absence of IRS lineage. (Q) Proliferation is unaffected following Gata3 ablation in TACs. Data are represented as mean±SEM. * = p<0.05, ** = p<0.01, *** = p<0.001, Students t-test. Scale bar = 25 μm.