Host muscle cell infiltration in cell-seeded plastic compressed collagen constructs.
J TISSUE ENG REGEN M
72 - 75.
Plastic compression enables rapid production of collagenous tissue like constructs without the need for cell based remodeling. We have previously reported testing spiral acellular and cell seeded constructs in-vivo. The constructs were implanted across the intercostal space of a lapine model designed to provide cyclical tensile loading in-vivo for up to 5 weeks. Results showed that cell seeded constructs elicit increased cellular infiltration, angiogenic response, mechanical integrity and decreased inflammatory response compared to acellular constructs. In this study the constructs were further tested for host muscle and nerve infiltration. Constructs were harvested, and stained for the myoblast marker desmin and neuronal marker neurofilament using an immunoperoxidase technique. We have found that host muscle cells start to migrate into the constructs by 3 weeks but did not reached the core of the spiral by 5 weeks, a delayed response. Significantly there is no innervation seen at 5 weeks in vivo in this model. Copyright (C) 2008 John Wiley & Sons, Ltd.
|Title:||Host muscle cell infiltration in cell-seeded plastic compressed collagen constructs|
|Keywords:||plastic compressed collagen, in vivo integration, innervation, host muscle cell infiltration, EXPRESS|
|UCL classification:||UCL > School of Life and Medical Sciences
UCL > School of Life and Medical Sciences > Faculty of Medical Sciences
UCL > School of Life and Medical Sciences > Faculty of Medical Sciences > Eastman Dental Institute
UCL > School of Life and Medical Sciences > Faculty of Medical Sciences > Surgery and Interventional Science (Division of)
UCL > School of Life and Medical Sciences > Faculty of Medical Sciences > Surgery and Interventional Science (Division of) > Institute of Orthopaedics and Musculoskeletal Science
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