| Literature DB >> 12531881 |
Susana Ortiz-Urda1, Qun Lin, Cheryl L Green, Douglas R Keene, M Peter Marinkovich, Paul A Khavari.
Abstract
Current therapeutic strategies for genetic skin disorders rely on the complex process of grafting genetically engineered tissue to recipient wound beds. Because fibroblasts synthesize and secrete extracellular matrix, we explored their utility in recessive dystrophic epidermolysis bullosa (RDEB), a blistering disease due to defective extracellular type VII collagen. Intradermal injection of RDEB fibroblasts overexpressing type VII collagen into intact RDEB skin stably restored correctly localized type VII collagen expression in vivo and normalized hallmark RDEB disease features, including subepidermal blistering and anchoring fibril defects. This article was published online in advance of the print edition. The date of publication is available from the JCI website, http://www.jci.org.Entities:
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Year: 2003 PMID: 12531881 PMCID: PMC151880 DOI: 10.1172/JCI17193
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808