{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,29]],"date-time":"2026-09-29T11:49:05Z","timestamp":1790682545941,"version":"4.1.0"},"reference-count":40,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2015,6,1]],"date-time":"2015-06-01T00:00:00Z","timestamp":1433116800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Photoderm Photoimm Photomed"],"published-print":{"date-parts":[[2015,9]]},"abstract":"<jats:title>Summary<\/jats:title><jats:sec><jats:title>Background<\/jats:title><jats:p>Skin scars and striae distensae (<jats:styled-content style=\"fixed-case\">SD<\/jats:styled-content>) are common dermal disorders with ill\u2010defined treatment options. There is emerging clinical evidence for use of photodynamic therapy (<jats:styled-content style=\"fixed-case\">PDT<\/jats:styled-content>) in treating skin fibrosis. Therefore, the aim here was to investigate the effect of <jats:styled-content style=\"fixed-case\">PDT<\/jats:styled-content> on skin scars and <jats:styled-content style=\"fixed-case\">SD<\/jats:styled-content> in an <jats:italic>ex\u00a0vivo<\/jats:italic> model of human skin scarring.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>Photodynamic therapy, with 5<jats:styled-content style=\"fixed-case\">ALA<\/jats:styled-content> or <jats:styled-content style=\"fixed-case\">MALA<\/jats:styled-content> in addition to illumination with 40\u00a0J\/cm<jats:sup>2<\/jats:sup> of red light, was applied to striae alba, fine line, hypertrophic and keloid scars <jats:italic>ex\u00a0vivo<\/jats:italic> (n\u00a0=\u00a018). General morphology was assessed by H&amp;E, Herovici's and Weigert's differential staining. Apoptosis, proliferation, metalloproteinase 3 and tropoelastin expression were quantified immunohistochemically, and differential gene expression of proliferating cell nuclear antigen (<jats:styled-content style=\"fixed-case\">PCNA<\/jats:styled-content>), collagen (<jats:styled-content style=\"fixed-case\">COL<\/jats:styled-content>) type I and type <jats:styled-content style=\"fixed-case\">III<\/jats:styled-content>, matrix metalloproteinase 3 (<jats:styled-content style=\"fixed-case\">MMP<\/jats:styled-content>3) and tropoelastin (<jats:styled-content style=\"fixed-case\">ELN<\/jats:styled-content>) was assessed by real\u2010time quantitative reverse transcription polymerase chain reaction.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Apoptosis increased, which correlated with decreased proliferation and <jats:styled-content style=\"fixed-case\">PCNA<\/jats:styled-content> gene expression. Post\u2010<jats:styled-content style=\"fixed-case\">PDT<\/jats:styled-content>, matrix components were found to be re\u2010organised in both hypertrophic and keloid scars. <jats:styled-content style=\"fixed-case\">COLI<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">COLIII<\/jats:styled-content> gene expression levels decreased, whilst <jats:styled-content style=\"fixed-case\">MMP<\/jats:styled-content>3 and <jats:styled-content style=\"fixed-case\">ELN<\/jats:styled-content> increased significantly post\u2010<jats:styled-content style=\"fixed-case\">PDT<\/jats:styled-content> compared to normal skin and untreated controls (<jats:italic>P<\/jats:italic>\u00a0&lt;\u00a00.05). However, no significant difference between 5<jats:styled-content style=\"fixed-case\">ALA<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">MALA<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">PDT<\/jats:styled-content> treatments was observed.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Using our unique <jats:italic>ex\u00a0vivo<\/jats:italic> model, we show for the first time morphological and cellular effect of application of <jats:styled-content style=\"fixed-case\">PDT<\/jats:styled-content>, which correlates with the degree and severity of dermal fibrosis. In view of this, <jats:styled-content style=\"fixed-case\">PDT<\/jats:styled-content> may be ideal in targeting treatment of abnormal skin scarring.<\/jats:p><\/jats:sec>","DOI":"10.1111\/phpp.12180","type":"journal-article","created":{"date-parts":[[2015,4,4]],"date-time":"2015-04-04T08:10:54Z","timestamp":1428135054000},"page":"239-251","source":"Crossref","is-referenced-by-count":35,"title":["<i>Ex vivo<\/i> evaluation of the effect of photodynamic therapy on skin scars and striae distensae"],"prefix":"10.1111","volume":"31","author":[{"given":"Jenifer","family":"Mendoza\u2010Garcia","sequence":"first","affiliation":[{"name":"Bioengineering Group School of Materials The University of Manchester Manchester UK"},{"name":"Plastic &amp; Reconstructive Surgery Research Group Manchester Institute of Biotechnology (MIB) The University of Manchester Manchester 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