<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Thriene, Kerstin</dc:creator>
  <dc:creator>Grüning, Björn Andreas</dc:creator>
  <dc:creator>Bornert, Olivier</dc:creator>
  <dc:creator>Erxleben, Anika</dc:creator>
  <dc:creator>Leppert, Juna</dc:creator>
  <dc:creator>Athanasiou, Ioannis</dc:creator>
  <dc:creator>Weber, Ekkehard</dc:creator>
  <dc:creator>Kiritsi, Dimitra</dc:creator>
  <dc:creator>Nyström, Alexander</dc:creator>
  <dc:creator>Reinheckel, Thomas</dc:creator>
  <dc:creator>Backofen, Rolf</dc:creator>
  <dc:creator>Has, Cristina</dc:creator>
  <dc:creator>Bruckner-Tuderman, Leena</dc:creator>
  <dc:creator>Dengjel, Jörn</dc:creator>
  <dc:date>2018-01-11</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The extracellular matrix protein collagen VII is part of the microenvironment of  stratified epithelia and critical in organismal homeostasis. Mutations in the encoding  gene COL7A1 lead to the skin disorder dystrophic epidermolysis bullosa (DEB), are  linked to skin fragility and progressive inflammation-driven fibrosis that facilitates  aggressive skin cancer. So far, these changes have been linked to mesenchymal  alterations, the epithelial consequences of collagen VII loss remaining under-  addressed. As epithelial dysfunction is a principal initiator of fibrosis, we performed a  comprehensive transcriptome and proteome profiling of primary human keratinocytes  to generate global and detailed images of dysregulated epidermal molecular pathways  linked to loss of collagen VII. These revealed downregulation of interaction partners of  collagen VII on mRNA and protein level, but also increased abundance of S100 pro-  inflammatory proteins in primary DEB keratinocytes. Increased TGF-β signaling due to  loss of collagen VII was associated with enhanced activity of lysosomal proteases in  both keratinocytes and skin of collagen VII-deficient individuals. Thus, loss of a single  structural protein, collagen VII, has extra- and intracellular consequences, resulting in  inflammatory processes that enable tissue destabilization and promote keratinocyte-  driven, progressive fibrosis.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/306229</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/306229/files/den_coa.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/306229/files/den_coa_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1074/mcp.RA117.000437</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Molecular &amp; Cellular Proteomics. - 2018, vol. 17, no. 4, p. 565-579</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Combinatorial omics analysis reveals perturbed lysosomal homeostasis in collagen VII-deficient keratinocytes</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
