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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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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•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.</description><identifier>ISSN: 0014-4800</identifier><identifier>EISSN: 1096-0945</identifier><identifier>DOI: 10.1016/j.yexmp.2014.03.002</identifier><identifier>PMID: 24662110</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>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</subject><ispartof>Experimental and molecular pathology, 2014-06, Vol.96 (3), p.316-327</ispartof><rights>2014 Elsevier Inc.</rights><rights>Copyright © 2014 Elsevier Inc. All rights reserved.</rights><rights>2014 Elsevier Inc. All rights reserved. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c459t-369566222a56f889deb0a4d2549676b55343267ef9b42d47e46edf267fd9d6d93</citedby><cites>FETCH-LOGICAL-c459t-369566222a56f889deb0a4d2549676b55343267ef9b42d47e46edf267fd9d6d93</cites><orcidid>0000-0003-0531-0481 ; 0000-0002-5886-5985</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.yexmp.2014.03.002$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24662110$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Joseph, Laurie B.</creatorcontrib><creatorcontrib>Heck, Diane E.</creatorcontrib><creatorcontrib>Cervelli, Jessica A.</creatorcontrib><creatorcontrib>Composto, Gabriella M.</creatorcontrib><creatorcontrib>Babin, Michael C.</creatorcontrib><creatorcontrib>Casillas, Robert P.</creatorcontrib><creatorcontrib>Sinko, Patrick J.</creatorcontrib><creatorcontrib>Gerecke, Donald R.</creatorcontrib><creatorcontrib>Laskin, Debra L.</creatorcontrib><creatorcontrib>Laskin, Jeffrey D.</creatorcontrib><title>Structural changes in hair follicles and sebaceous glands of hairless mice following exposure to sulfur mustard</title><title>Experimental and molecular pathology</title><addtitle>Exp Mol Pathol</addtitle><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.</description><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>Caspase 3 - genetics</subject><subject>Caspase 3 - metabolism</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Proliferation - drug effects</subject><subject>Disease Models, Animal</subject><subject>DNA Damage - drug effects</subject><subject>Down-Regulation</subject><subject>Epithelial Cells - drug effects</subject><subject>Galectin 3 - genetics</subject><subject>Galectin 3 - metabolism</subject><subject>Hair Follicle - drug effects</subject><subject>Hair Follicle - pathology</subject><subject>Hair follicles</subject><subject>Histones - genetics</subject><subject>Histones - metabolism</subject><subject>Keratinocytes - drug effects</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Hairless</subject><subject>Mustard Gas - toxicity</subject><subject>Phosphorylated histone H2A.X</subject><subject>Receptor, Fibroblast Growth Factor, Type 2 - genetics</subject><subject>Receptor, Fibroblast Growth Factor, Type 2 - metabolism</subject><subject>Sebaceous glands</subject><subject>Sebaceous Glands - drug effects</subject><subject>Sebaceous Glands - pathology</subject><subject>Skin - drug effects</subject><subject>Skin - pathology</subject><subject>Sulfur mustard</subject><subject>Wound Healing - drug effects</subject><issn>0014-4800</issn><issn>1096-0945</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UM1u1DAQthCIbgtPgIT8AknHjuOsD1Sqqv4gVeIAnC3HHu96lcQrOynt29fdhQounEYz38_MfIR8YlAzYPJ8Vz_h47ivOTBRQ1MD8DdkxUDJCpRo35IVFKQSa4ATcprzDgAUMP6enHAhJWcMViR-n9Ni5yWZgdqtmTaYaZjo1oREfRyGYIcyMZOjGXtjMS6ZbobSZxr9gVbwTMdg8cCPv8K0ofi4j3lJSOdI8zL4JdFxybNJ7gN5582Q8ePvekZ-3lz_uLqr7r_dfr26vK-saNVcNVK15UTOTSv9eq0c9mCE461QspN92zai4bJDr3rBnehQSHS-TLxTTjrVnJGLo-9-6Ud0Fqe5vKj3KYwmPelogv4XmcJWb-KDFowD77pi0BwNbIo5J_SvWgb6JX-904f89Uv-Ghpd8i-qz3-vfdX8CbwQvhwJWJ5_CJh0tgEniy4ktLN2Mfx3wTMnbZtg</recordid><startdate>20140601</startdate><enddate>20140601</enddate><creator>Joseph, Laurie B.</creator><creator>Heck, Diane E.</creator><creator>Cervelli, Jessica A.</creator><creator>Composto, Gabriella M.</creator><creator>Babin, Michael C.</creator><creator>Casillas, Robert P.</creator><creator>Sinko, Patrick J.</creator><creator>Gerecke, Donald R.</creator><creator>Laskin, Debra L.</creator><creator>Laskin, Jeffrey D.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0531-0481</orcidid><orcidid>https://orcid.org/0000-0002-5886-5985</orcidid></search><sort><creationdate>20140601</creationdate><title>Structural changes in hair follicles and sebaceous glands of hairless mice following exposure to sulfur mustard</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c459t-369566222a56f889deb0a4d2549676b55343267ef9b42d47e46edf267fd9d6d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Apoptosis - drug effects</topic><topic>Caspase 3 - genetics</topic><topic>Caspase 3 - metabolism</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell Proliferation - drug effects</topic><topic>Disease Models, Animal</topic><topic>DNA Damage - drug effects</topic><topic>Down-Regulation</topic><topic>Epithelial Cells - drug effects</topic><topic>Galectin 3 - genetics</topic><topic>Galectin 3 - metabolism</topic><topic>Hair Follicle - drug effects</topic><topic>Hair Follicle - pathology</topic><topic>Hair follicles</topic><topic>Histones - genetics</topic><topic>Histones - metabolism</topic><topic>Keratinocytes - drug effects</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Hairless</topic><topic>Mustard Gas - toxicity</topic><topic>Phosphorylated histone H2A.X</topic><topic>Receptor, Fibroblast Growth Factor, Type 2 - genetics</topic><topic>Receptor, Fibroblast Growth Factor, Type 2 - metabolism</topic><topic>Sebaceous glands</topic><topic>Sebaceous Glands - drug effects</topic><topic>Sebaceous Glands - pathology</topic><topic>Skin - drug effects</topic><topic>Skin - pathology</topic><topic>Sulfur mustard</topic><topic>Wound Healing - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Joseph, Laurie B.</creatorcontrib><creatorcontrib>Heck, Diane E.</creatorcontrib><creatorcontrib>Cervelli, Jessica A.</creatorcontrib><creatorcontrib>Composto, Gabriella M.</creatorcontrib><creatorcontrib>Babin, Michael C.</creatorcontrib><creatorcontrib>Casillas, Robert P.</creatorcontrib><creatorcontrib>Sinko, Patrick J.</creatorcontrib><creatorcontrib>Gerecke, Donald R.</creatorcontrib><creatorcontrib>Laskin, Debra L.</creatorcontrib><creatorcontrib>Laskin, Jeffrey D.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Experimental and molecular pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Joseph, Laurie B.</au><au>Heck, Diane E.</au><au>Cervelli, Jessica A.</au><au>Composto, Gabriella M.</au><au>Babin, Michael C.</au><au>Casillas, Robert P.</au><au>Sinko, Patrick J.</au><au>Gerecke, Donald R.</au><au>Laskin, Debra L.</au><au>Laskin, Jeffrey D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural changes in hair follicles and sebaceous glands of hairless mice following exposure to sulfur mustard</atitle><jtitle>Experimental and molecular pathology</jtitle><addtitle>Exp Mol Pathol</addtitle><date>2014-06-01</date><risdate>2014</risdate><volume>96</volume><issue>3</issue><spage>316</spage><epage>327</epage><pages>316-327</pages><issn>0014-4800</issn><eissn>1096-0945</eissn><abstract>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.</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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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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