Structural changes in the skin of hairless mice following exposure to sulfur mustard correlate with inflammation and DNA damage

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• 作者：Laurie B.  ; Joseph^a ; Donald R.  ; Gerecke^a ; Diane E.  ; Heck^b ; Adrienne T.  ; Black^a ; Patrick J.  ; Sinko^c ; Jessica A.  ; Cervelli^a ; Robert P.  ; Casillas^d ; Michael C.  ; Babin^e ; Debra L.  ; Laskin^a ; Jeffrey D.  ; Laskin^f ;   ; ^{jlaskin@eohsi.rutgers.edu}
• 关键词：Sulfur mustard ; Skin ; Phosphorylated histone 2A.X ; Cyclooxygenase-2 ; Mast cells
• 刊名：Experimental and Molecular Pathology
• 出版年：2011
• 出版时间：October 2011
• 年：2011
• 卷：91
• 期：2
• 页码：515-527
• 全文大小：3611 K

文摘

Sulfur mustard (SM, bis(2-chloroethyl)sulfide) is a bifunctional alkylating agent that causes dermal inflammation, edema and blistering. To investigate the pathogenesis of SM-induced injury, we used a vapor cup model which provides an occlusive environment in which SM is in constant contact with the skin. The dorsal skin of SKH-1 hairless mice was exposed to saturated SM vapor or air control. Histopathological changes, inflammatory markers and DNA damage were analyzed 1?4 days later. After 1 day, SM caused epidermal thinning, stratum corneum shedding, basal cell karyolysis, hemorrhage and macrophage and neutrophil accumulation in the dermis. Cleaved caspase-3 and phosphorylated histone 2A.X (phospho-H2A.X), markers of apoptosis and DNA damage, respectively, were increased whereas proliferating cell nuclear antigen (PCNA) was down-regulated after SM exposure. By 3 days, epithelial cell hypertrophy, edema, parakeratosis and loss of epidermal structures were noted. Enzymes generating pro-inflammatory mediators including myeloperoxidase and cyclooxygenase-2 were upregulated. After 7 days, keratin-10, a differentiation marker, was evident in the stratum corneum. This was associated with an underlying eschar, as neoepidermis began to migrate at the wound edges. Trichrome staining revealed increased collagen deposition in the dermis. PCNA expression in the epidermis was correlated with hyperplasia, hyperkeratosis, and parakeratosis. By 14 days, there was epidermal regeneration with extensive hyperplasia, and reduced expression of cleaved caspase-3, cyclooxygenase-2 and phospho-H2A.X. These findings are consistent with the pathophysiology of SM-induced skin injury in humans suggesting that the hairless mouse can be used to investigate the dermatoxicity of vesicants and the potential efficacy of countermeasures.