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Biochemistry & Molecular Biology

Telogen elongation in the hair cycle of ob/ob mice

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Pages 74-79 | Received 03 Apr 2015, Accepted 15 Jun 2015, Published online: 04 Aug 2015

Figures & data

Fig. 1. Identification of anagen hair follicles by HE staining (A) and immunohistochemistry for Ki67 (B).

Notes: Anagen follicles extended into the subcutaneous fat layer and the dermal papilla was enveloped with hair bulb. Lots of proliferative cells were observed in anagen follicles. hs: hair shaft, br: bulge region, hb: hair bulb, and sf: subcutaneous fat layer. Arrows indicate the Ki67-positive follicular cells. Bar = 300 μm in A and 100 μm in B.
Fig. 1. Identification of anagen hair follicles by HE staining (A) and immunohistochemistry for Ki67 (B).

Table 1. Histologically identified hair cycle phases and positivity for Ki67 in +/+ mice.

Table 2. Histologically identified hair cycle phases and Ki67 positivity in ob/ob mice.

Fig. 2. Anagen transition in +/+ and ob/ob mice.

Notes: (A)–(C): Macroscopic observation of the anagen transition, which is recognized as the skin pigmentation. Arrows indicate the abnormal pigmentation of skin in ob/ob mice. Bar = 1 cm. (D)–(E): Histological observation of hair follicles in the ob/ob mice shown in C. The anagen follicles and the catagen follicles were coexisted in the HE-stained skin tissue with pigmentation (D). The caudal tissue showed only the telogen follicles (E). Bar = 300 μm.
Fig. 2. Anagen transition in +/+ and ob/ob mice.

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