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. 2013 Jul 19;8(7):e69368. doi: 10.1371/journal.pone.0069368

Figure 2. Egfr mutant follicles did not progress through catagen following cyclophosphamide.

Figure 2

Hematoxylin and eosin stained sections from mutant (panels on right) and control (panels on left) mice after cyclophosphamide (B-D) or vehicle (A). Vehicle mice displayed anagen 2d post-injection (A, arrowheads). Egfr controls (B left) exhibited follicular distortion (arrowhead) and regression, while mutants (B right) had follicular distortion (arrowhead) at 2 d after cyclophosphamide. By 4d, controls (C left) displayed late dystrophic catagen, while mutants (C right) maintained elongated follicles (arrowhead). Controls initiated secondary recovery with anagen by 8 d (D left), indicated by the bulb position at dermis and subcutis border (arrowhead). Mutant follicles retained hair at 8 d (D right, arrowhead). Scale bar indicates 100 µm.