Figure 1.
The participation of K15+ and Lgr5+ HFSCs in SG renewal in the depilation-induced hair cycle
(A) Experimental timeline of tamoxifen/RU486 injection in 3-weeks old (3W) Lgr5:mTmG and K15:mTmG mice. P, postpartum; D, day.
(B) Representative images showing the fate of K15-lineage cells (green) during the hair cycle in 3W K15:mTmG mice.
(C) Quantitation of mGFP+ cells within SGs in K15:mTmG mice in the first hair cycle. Data are represented as mean ± SEM, ns, not significant, ∗p < 0.05, ∗∗∗p < 0.005, t-test, n = 3.
(D and E) Tracing of progenies of Lgr5+ HFSCs in Lgr5:mTmG mice after tamoxifen induction from P23 to P58 (D), and in the second hair cycle (E).
(F) Experimental scheme for RU486/tamoxifen injection and analysis of depilation-induced HF activation in K15:mTmG or Lgr5:mTmG mice.
(G) Tracing of K15+ HFSCs in K15:mTmG mice from P60 to P80 after RU486 induction.
(H) Quantitation of mGFP+ cells within SGs in 8W K15:mTmG mice at the first cycle. Data are represented as mean ± SEM, ns, not significant, ∗p < 0.05, t-test, n = 3.
(I) A schematic diagram showing the progeny of K15+ SCs in the depilation-induced hair cycle.
(J and K) Tracing the fate of Lgr5+ HFSCs in Lgr5:mTmG mice in the first (0–35 days) (J) and the second (40–75 days) (K) hair cycle following tamoxifen treatment.
(L) Quantitation of mGFP+ cells within SGs in 8W Lgr5:mTmG mice at the second cycle. Data are represented as mean ± SEM, ∗p < 0.05, ∗∗∗p < 0.005, t-test, n = 3.
(M) A schematic portraying the fate of Lgr5+ HFSCs in two consecutive hair cycles induced by depilation. Bu, Bulge; DP, dermal papilla; SG, sebaceous gland. Scale bars: 50 μm.