| Literature DB >> 18660817 |
Cesare Gargioli1, Marcello Coletta, Fabrizio De Grandis, Stefano M Cannata, Giulio Cossu.
Abstract
Sclerosis and reduced microvessel density characterize advanced stages of muscular dystrophy and hamper cell or gene delivery, precluding treatment of most individuals with Duchenne muscular dystrophy. Modified tendon fibroblasts expressing an angiogenic factor (placenta growth factor, PlGF) and a metalloproteinase (matrix metalloproteinase-9, MMP-9) are able to restore a vascular network and reduce collagen deposition, allowing efficient cell therapy in aged dystrophic mice. These data open the possibility of extending new therapies to currently untreatable individuals.Entities:
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Year: 2008 PMID: 18660817 DOI: 10.1038/nm.1852
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 53.440