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Relationship between expression of tight junction-related molecules and perturbed epidermal barrier function in UVB-irradiated hairless mice
In epithelia, tight junctions (TJs) create a primary barrier to the diffusion of solutes through the paracellular pathway. Although TJ-related molecules are present in the epidermis, the precise mechanisms underlying TJ functions in this tissue remain unclear. In this study, we use an ultraviolet (U...
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Published in: | Archives of Dermatological Research 2008-02, Vol.300 (2), p.61-68 |
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description | In epithelia, tight junctions (TJs) create a primary barrier to the diffusion of solutes through the paracellular pathway. Although TJ-related molecules are present in the epidermis, the precise mechanisms underlying TJ functions in this tissue remain unclear. In this study, we use an ultraviolet (UV) B-irradiated murine skin model, in which the epidermal barrier function has been perturbed, to demonstrate a correlation between the expression patterns of TJ-related molecules and the epidermal permeability of TJs. Occludin remained localized in the upper epidermis, regardless of UVB irradiation (0.15 J per cm
2
). ZO-1 was localized in the upper portion of normal epidermis, and within 3–4 days of UVB irradiation, it was expressed throughout the upper epidermis and their expression coincided with epidermal thickening. Protein expression of claudin-1 and occludin did not alter until 3 and 4 days after UVB irradiation, respectively and thereafter expression remained elevated above pre-irradiation levels. An in vivo epidermal permeability assay revealed that tight junction-barrier function was perturbed by UVB irradiation, whereby biotinylated markers clearly permeated the stratum granulosum 3–5 days after irradiation. These results suggest that TJ-related molecules play important roles in epidermal barrier function in murine skin and show that changes in their expression patterns are associated with epidermal barrier perturbation after UVB irradiation. Specifically, it appears that epidermal barrier recovery is accelerated by the increased production and dense localization of occludin in the cell–cell contact region of the stratum granulosum. |
doi_str_mv | 10.1007/s00403-007-0817-y |
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2
). ZO-1 was localized in the upper portion of normal epidermis, and within 3–4 days of UVB irradiation, it was expressed throughout the upper epidermis and their expression coincided with epidermal thickening. Protein expression of claudin-1 and occludin did not alter until 3 and 4 days after UVB irradiation, respectively and thereafter expression remained elevated above pre-irradiation levels. An in vivo epidermal permeability assay revealed that tight junction-barrier function was perturbed by UVB irradiation, whereby biotinylated markers clearly permeated the stratum granulosum 3–5 days after irradiation. These results suggest that TJ-related molecules play important roles in epidermal barrier function in murine skin and show that changes in their expression patterns are associated with epidermal barrier perturbation after UVB irradiation. Specifically, it appears that epidermal barrier recovery is accelerated by the increased production and dense localization of occludin in the cell–cell contact region of the stratum granulosum.</description><identifier>ISSN: 0340-3696</identifier><identifier>EISSN: 1432-069X</identifier><identifier>DOI: 10.1007/s00403-007-0817-y</identifier><identifier>PMID: 18064478</identifier><identifier>CODEN: ADREDL</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Animals ; Biological and medical sciences ; Claudin-1 ; Dermatology ; Epidermis - metabolism ; Epidermis - pathology ; Epidermis - radiation effects ; Gene Expression - radiation effects ; Immunohistochemistry ; Male ; Medical sciences ; Medicine ; Medicine & Public Health ; Membrane Proteins - genetics ; Membrane Proteins - metabolism ; Mice ; Mice, Hairless ; Microscopy, Electron, Transmission ; Occludin ; Original Paper ; Permeability - radiation effects ; Phosphoproteins - genetics ; Phosphoproteins - metabolism ; Recovery of Function - radiation effects ; Tight Junctions - metabolism ; Tight Junctions - radiation effects ; Ultraviolet Rays - adverse effects ; Zonula Occludens-1 Protein</subject><ispartof>Archives of Dermatological Research, 2008-02, Vol.300 (2), p.61-68</ispartof><rights>Springer-Verlag 2007</rights><rights>2008 INIST-CNRS</rights><rights>Springer-Verlag 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c465t-6b8a96f44bf166a60409d76fe3e8982c0af1467bc022d7512339c439ece3ca373</citedby><cites>FETCH-LOGICAL-c465t-6b8a96f44bf166a60409d76fe3e8982c0af1467bc022d7512339c439ece3ca373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20031079$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18064478$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamamoto, Takuya</creatorcontrib><creatorcontrib>Kurasawa, Masumi</creatorcontrib><creatorcontrib>Hattori, Takao</creatorcontrib><creatorcontrib>Maeda, Tetsuo</creatorcontrib><creatorcontrib>Nakano, Hiroyuki</creatorcontrib><creatorcontrib>Sasaki, Hiroyuki</creatorcontrib><title>Relationship between expression of tight junction-related molecules and perturbed epidermal barrier function in UVB-irradiated hairless mice</title><title>Archives of Dermatological Research</title><addtitle>Arch Dermatol Res</addtitle><addtitle>Arch Dermatol Res</addtitle><description>In epithelia, tight junctions (TJs) create a primary barrier to the diffusion of solutes through the paracellular pathway. Although TJ-related molecules are present in the epidermis, the precise mechanisms underlying TJ functions in this tissue remain unclear. In this study, we use an ultraviolet (UV) B-irradiated murine skin model, in which the epidermal barrier function has been perturbed, to demonstrate a correlation between the expression patterns of TJ-related molecules and the epidermal permeability of TJs. Occludin remained localized in the upper epidermis, regardless of UVB irradiation (0.15 J per cm
2
). ZO-1 was localized in the upper portion of normal epidermis, and within 3–4 days of UVB irradiation, it was expressed throughout the upper epidermis and their expression coincided with epidermal thickening. Protein expression of claudin-1 and occludin did not alter until 3 and 4 days after UVB irradiation, respectively and thereafter expression remained elevated above pre-irradiation levels. An in vivo epidermal permeability assay revealed that tight junction-barrier function was perturbed by UVB irradiation, whereby biotinylated markers clearly permeated the stratum granulosum 3–5 days after irradiation. These results suggest that TJ-related molecules play important roles in epidermal barrier function in murine skin and show that changes in their expression patterns are associated with epidermal barrier perturbation after UVB irradiation. Specifically, it appears that epidermal barrier recovery is accelerated by the increased production and dense localization of occludin in the cell–cell contact region of the stratum granulosum.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Claudin-1</subject><subject>Dermatology</subject><subject>Epidermis - metabolism</subject><subject>Epidermis - pathology</subject><subject>Epidermis - radiation effects</subject><subject>Gene Expression - radiation effects</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - metabolism</subject><subject>Mice</subject><subject>Mice, Hairless</subject><subject>Microscopy, Electron, Transmission</subject><subject>Occludin</subject><subject>Original Paper</subject><subject>Permeability - radiation effects</subject><subject>Phosphoproteins - genetics</subject><subject>Phosphoproteins - metabolism</subject><subject>Recovery of Function - radiation effects</subject><subject>Tight Junctions - metabolism</subject><subject>Tight Junctions - radiation effects</subject><subject>Ultraviolet Rays - adverse effects</subject><subject>Zonula Occludens-1 Protein</subject><issn>0340-3696</issn><issn>1432-069X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp1kcuKFTEQhoMozmGcB3AjQdBdtHKZpLPUwRsMCOKIu5BOV8_JoW8m3eh5Bx_a9JzGAcFsUlS-_68iPyFPObziAOZ1BlAgWSkZVNyw4wOy40oKBtp-f0h2IBUwqa0-Ixc5H6AcA0qAeUzOeAVaKVPtyO8v2Pk5jkPex4nWOP9EHCj-mhLmXNp0bOkcb_czPSxDWEGWVgU2tB87DEuHmfqhoROmeUl16eMUG0y972jtU4qYaLtJaRzozbe3LKbkm3hnsvcxFYtM-xjwCXnU-i7jxXafk5v3775efWTXnz98unpzzYLSlzPTdeWtbpWqW6611-UfbGN0ixIrW4kAvuVKmzqAEI255EJKG5S0GFAGL408Jy9PvlMafyyYZ9fHHLDr_IDjkp0BAZU1toDP_wEP45KGspsTXAiwVosC8RMU0phzwtZNKfY-HR0Ht0blTlG5tVyjcseiebYZL3WPzb1iC6YALzbA5-C7NvkhxPyXEwCSw92G4sTl8jTcYrrf8P_T_wAf7K5E</recordid><startdate>20080201</startdate><enddate>20080201</enddate><creator>Yamamoto, Takuya</creator><creator>Kurasawa, Masumi</creator><creator>Hattori, Takao</creator><creator>Maeda, Tetsuo</creator><creator>Nakano, Hiroyuki</creator><creator>Sasaki, Hiroyuki</creator><general>Springer-Verlag</general><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><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>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20080201</creationdate><title>Relationship between expression of tight junction-related molecules and perturbed epidermal barrier function in UVB-irradiated hairless mice</title><author>Yamamoto, Takuya ; Kurasawa, Masumi ; Hattori, Takao ; Maeda, Tetsuo ; Nakano, Hiroyuki ; Sasaki, Hiroyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-6b8a96f44bf166a60409d76fe3e8982c0af1467bc022d7512339c439ece3ca373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Claudin-1</topic><topic>Dermatology</topic><topic>Epidermis - metabolism</topic><topic>Epidermis - pathology</topic><topic>Epidermis - radiation effects</topic><topic>Gene Expression - radiation effects</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Membrane Proteins - genetics</topic><topic>Membrane Proteins - metabolism</topic><topic>Mice</topic><topic>Mice, Hairless</topic><topic>Microscopy, Electron, Transmission</topic><topic>Occludin</topic><topic>Original Paper</topic><topic>Permeability - radiation effects</topic><topic>Phosphoproteins - genetics</topic><topic>Phosphoproteins - metabolism</topic><topic>Recovery of Function - radiation effects</topic><topic>Tight Junctions - metabolism</topic><topic>Tight Junctions - radiation effects</topic><topic>Ultraviolet Rays - adverse effects</topic><topic>Zonula Occludens-1 Protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamamoto, Takuya</creatorcontrib><creatorcontrib>Kurasawa, Masumi</creatorcontrib><creatorcontrib>Hattori, Takao</creatorcontrib><creatorcontrib>Maeda, Tetsuo</creatorcontrib><creatorcontrib>Nakano, Hiroyuki</creatorcontrib><creatorcontrib>Sasaki, Hiroyuki</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of Dermatological Research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamamoto, Takuya</au><au>Kurasawa, Masumi</au><au>Hattori, Takao</au><au>Maeda, Tetsuo</au><au>Nakano, Hiroyuki</au><au>Sasaki, Hiroyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Relationship between expression of tight junction-related molecules and perturbed epidermal barrier function in UVB-irradiated hairless mice</atitle><jtitle>Archives of Dermatological Research</jtitle><stitle>Arch Dermatol Res</stitle><addtitle>Arch Dermatol Res</addtitle><date>2008-02-01</date><risdate>2008</risdate><volume>300</volume><issue>2</issue><spage>61</spage><epage>68</epage><pages>61-68</pages><issn>0340-3696</issn><eissn>1432-069X</eissn><coden>ADREDL</coden><abstract>In epithelia, tight junctions (TJs) create a primary barrier to the diffusion of solutes through the paracellular pathway. Although TJ-related molecules are present in the epidermis, the precise mechanisms underlying TJ functions in this tissue remain unclear. In this study, we use an ultraviolet (UV) B-irradiated murine skin model, in which the epidermal barrier function has been perturbed, to demonstrate a correlation between the expression patterns of TJ-related molecules and the epidermal permeability of TJs. Occludin remained localized in the upper epidermis, regardless of UVB irradiation (0.15 J per cm
2
). ZO-1 was localized in the upper portion of normal epidermis, and within 3–4 days of UVB irradiation, it was expressed throughout the upper epidermis and their expression coincided with epidermal thickening. Protein expression of claudin-1 and occludin did not alter until 3 and 4 days after UVB irradiation, respectively and thereafter expression remained elevated above pre-irradiation levels. An in vivo epidermal permeability assay revealed that tight junction-barrier function was perturbed by UVB irradiation, whereby biotinylated markers clearly permeated the stratum granulosum 3–5 days after irradiation. These results suggest that TJ-related molecules play important roles in epidermal barrier function in murine skin and show that changes in their expression patterns are associated with epidermal barrier perturbation after UVB irradiation. Specifically, it appears that epidermal barrier recovery is accelerated by the increased production and dense localization of occludin in the cell–cell contact region of the stratum granulosum.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>18064478</pmid><doi>10.1007/s00403-007-0817-y</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Claudin-1 Dermatology Epidermis - metabolism Epidermis - pathology Epidermis - radiation effects Gene Expression - radiation effects Immunohistochemistry Male Medical sciences Medicine Medicine & Public Health Membrane Proteins - genetics Membrane Proteins - metabolism Mice Mice, Hairless Microscopy, Electron, Transmission Occludin Original Paper Permeability - radiation effects Phosphoproteins - genetics Phosphoproteins - metabolism Recovery of Function - radiation effects Tight Junctions - metabolism Tight Junctions - radiation effects Ultraviolet Rays - adverse effects Zonula Occludens-1 Protein |
title | Relationship between expression of tight junction-related molecules and perturbed epidermal barrier function in UVB-irradiated hairless mice |
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