<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>He, Yinghong</dc:creator>
  <dc:creator>Thriene, Kerstin</dc:creator>
  <dc:creator>Boerries, Melanie</dc:creator>
  <dc:creator>Hausser, Ingrid</dc:creator>
  <dc:creator>Franzke, Claus-Werner</dc:creator>
  <dc:creator>Busch, Hauke</dc:creator>
  <dc:creator>Dengjel, Jörn</dc:creator>
  <dc:creator>Has, Cristina</dc:creator>
  <dc:date>2018-12-01</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Integrin α3β1, a major epidermal adhesion receptor is critical for organization of the  basement membrane during development and wound healing. Integrin α3 deficiency  leads to interstitial lung disease, nephrotic syndrome and epidermolysis bullosa  (ILNEB), an autosomal recessive multiorgan disease characterized by basement  membrane abnormalities in skin, lung and kidney. The pathogenetic chains from  ITGA3 mutation to tissue abnormalities are still unclear. Although integrin α3 was  reported to regulate multiple extracellular proteins, the composition of the extracellular  compartment of integrin α3-negative keratinocytes has not been resolved so far. In a  comprehensive approach, quantitative proteomics of deposited extracellular matrix,  conditioned cultured media as well as of the intracellular compartment of  keratinocytes isolated from an ILNEB patient and from normal skin were performed.  By mass spectrometry-based proteomics, 167 proteins corresponding to the GO terms  “extracellular” and “cell adhesion”, or included in the “human matrisome” were  identified in the deposited extracellular matrix, and 217 in the conditioned media of  normal human keratinocytes. In the absence of integrin α3, 33% and 26% respectively  were dysregulated. Dysregulated proteins were functionally related to integrin α3 or  were known interaction partners. The results show that in the absence of integrin α3  ILNEB keratinocytes produce a fibronectin-rich microenvironment and make use of  fibronectin-binding integrin subunits αv and α5. The most important results were  validated in monolayer and organotypic coculture models. Finally, the in vivo  relevance of the most dysregulated components was demonstrated by  immunostainings of skin, kidney and lung samples of three ILNEB patients.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/307350</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/307350/files/den_cae.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/j.matbio.2018.07.001</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Matrix Biology. - 2018, vol. 74, p. 62-76</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Constitutional absence of epithelial integrin α3 impacts the composition of the cellular microenvironment of ILNEB keratinocytes</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
