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Initially thought to act only as a scaffold, the ECM is now known to provide a myriad of signals to cells regulating all aspects of their phenotype from morphology to differentiation. Matricellular proteins are a class of ECM related molecules defined through their ability to modulate cell\u2013matrix interactions. Matricellular proteins are expressed at high levels during development, but typically only appear in postnatal tissue in wound repair or disease, where their levels increase substantially. Members of the CCN family, tenascin\u2010C, osteopontin, secreted protein acidic rich in cysteine (SPARC), bone sialoprotein, thrombospondins, and galectins have all been classed as matricellular proteins. Periostin, a 90 kDa secreted homophilic cell adhesion protein, was recently added to matricellular class of proteins based on its expression pattern and function during development as well as in wound repair. Periostin is expressed in connective tissues including the periodontal ligament, tendons, skin and bone, and is also prominent in neoplastic tissues, cardiovascular disease, as well as in connective tissue wound repair. This review will focus on the functional role of periostin in tissue physiology. Fundamentally, it appears that periostin influences cell behaviour as well as collagen fibrillogenesis, and therefore exerts control over the structural and functional properties of connective tissues in both health and disease. Periostin is a novel matricellular protein with close homology to <jats:italic>Drosophila fasciclin 1.<\/jats:italic> In this review, the functional role of periostin is discussed in the context of connective tissue physiology, in development, disease, and wound repair.<\/jats:p>","DOI":"10.1007\/s12079-008-0023-5","type":"journal-article","created":{"date-parts":[[2008,7,19]],"date-time":"2008-07-19T17:21:11Z","timestamp":1216488071000},"page":"9-17","source":"Crossref","is-referenced-by-count":171,"title":["Functional role of periostin in development and wound repair: implications for connective tissue disease"],"prefix":"10.1002","volume":"2","author":[{"given":"Douglas W.","family":"Hamilton","sequence":"first","affiliation":[{"name":"CIHR Group in Skeletal Development &amp; Remodeling Schulich School of Medicine and Dentistry Dental Sciences Building University of Western Ontario N6A 5C1 London Ontario 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