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

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 gla...

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Veröffentlicht in:Experimental and molecular pathology 2014-06, Vol.96 (3), p.316-327
Hauptverfasser: 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.
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container_end_page 327
container_issue 3
container_start_page 316
container_title Experimental and molecular pathology
container_volume 96
creator 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.
description 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.
doi_str_mv 10.1016/j.yexmp.2014.03.002
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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. 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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.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>24662110</pmid><doi>10.1016/j.yexmp.2014.03.002</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-0531-0481</orcidid><orcidid>https://orcid.org/0000-0002-5886-5985</orcidid><oa>free_for_read</oa></addata></record>
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
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
title Structural changes in hair follicles and sebaceous glands of hairless mice following exposure to sulfur mustard
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