Structural changes in hair follicles and sebaceous glands of hairless mice following exposure to sulfur mustard

• Published in: Experimental and molecular pathology Vol. 96; no. 3; pp. 316 - 327
• Main Authors: Joseph, Laurie B., Heck, Diane E., Cervelli, Jessica A., Composto, Gabriella M., Babin, Michael C., Casillas, Robert P., Sinko, Patrick J., Gerecke, Donald R., Laskin, Debra L., Laskin, Jeffrey D.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 01.06.2014
• Subjects: Animals; Apoptosis - drug effects; Caspase 3 - genetics; Caspase 3 - metabolism; Cell Differentiation - drug effects; Cell Proliferation - drug effects; Disease Models, Animal; DNA Damage - drug effects; Down-Regulation; Epithelial Cells - drug effects; Galectin 3 - genetics; Galectin 3 - metabolism; Hair Follicle - drug effects; Hair Follicle - pathology; Hair follicles; Histones - genetics; Histones - metabolism; Keratinocytes - drug effects; Male; Mice; Mice, Hairless; Mustard Gas - toxicity; Phosphorylated histone H2A.X; Receptor, Fibroblast Growth Factor, Type 2 - genetics; Receptor, Fibroblast Growth Factor, Type 2 - metabolism; Sebaceous glands; Sebaceous Glands - drug effects; Sebaceous Glands - pathology; Skin - drug effects; Skin - pathology; Sulfur mustard; Wound Healing - drug effects; Sebaceous glands; PCNA; Phospho-H2A.X; H&E; Sulfur mustard; SM; Hair follicles; FGFR2; Phosphorylated histone H2A.X
• ISSN: 0014-4800; 1096-0945
• DOI: 10.1016/j.yexmp.2014.03.002

Sulfur mustard (SM) is a bifunctional alkylating agent causing skin inflammation, edema and blistering. A hallmark of SM-induced toxicity is follicular and interfollicular epithelial damage. In the present studies we determined if SM-induced structural alterations in hair follicles and sebaceous glands were correlated with cell damage, inflammation and wound healing. The dorsal skin of hairless mice was treated with saturated SM vapor. One to seven days later, epithelial cell karyolysis within the hair root sheath, infundibulum and isthmus was apparent, along with reduced numbers of sebocytes. Increased numbers of utriculi, some with connections to the skin surface, and engorged dermal cysts were also evident. This was associated with marked changes in expression of markers of DNA damage (phospho-H2A.X), apoptosis (cleaved caspase-3), and wound healing (FGFR2 and galectin-3) throughout pilosebaceous units. Conversely, fatty acid synthase and galectin-3 were down-regulated in sebocytes after SM. Decreased numbers of hair follicles and increased numbers of inflammatory cells surrounding the utriculi and follicular cysts were noted within the wound 3–7days post-SM exposure. Expression of phospho-H2A.X, cleaved caspase-3, FGFR2 and galectin-3 was decreased in dysplastic follicular epidermis. Fourteen days after SM, engorged follicular cysts which expressed galectin-3 were noted within hyperplastic epidermis. Galectin-3 was also expressed in basal keratinocytes and in the first few layers of suprabasal keratinocytes in neoepidermis formed during wound healing indicating that this lectin is important in the early stages of keratinocyte differentiation. These data indicate that hair follicles and sebaceous glands are targets for SM in the skin. •Hairless mice have dystrophic hair follicles and sebaceous glands.•DNA damage in hair follicles and sebocytes is induced by sulfur mustard.•Sulfur mustard alters fatty acid synthase and causes sebocyte maturation.•Sulfur mustard causes follicular degeneration.