| Literature DB >> 25617491 |
Johannes Prox1, Philipp Arnold2, Christoph Becker-Pauly3.
Abstract
Metalloproteases meprin α and meprin β were recently discovered as procollagen proteinases, capable of cleaving off the globular C- and N-terminal prodomains of fibrillar collagen type I and type III. This proteolytic process is indeed sufficient to induce collagen fibril assembly as visualized by transmission electron microscopy. The biological relevance was demonstrated with the help of meprin α and meprin β knock-out mice, which exhibit decreased collagen deposition in skin resulting in impaired tensile strength. On the other hand, overexpression of meprin metalloproteases was found under fibrotic conditions in the skin (keloids) and the lung (pulmonary hypertension). Thus, regulation of meprin activity by specific inhibition to reduce collagen maturation might be a suitable approach for the treatment of certain pathological conditions.Entities:
Keywords: Collagen assembly; Fibrosis; Meprin α; Meprin β; Metalloprotease; Procollagen proteinase
Mesh:
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Year: 2015 PMID: 25617491 DOI: 10.1016/j.matbio.2015.01.010
Source DB: PubMed Journal: Matrix Biol ISSN: 0945-053X Impact factor: 11.583