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      The biodegradability of electrospun Dextran/PLGA scaffold in a fibroblast/macrophage co-culture.

      1 , ,
      Biomaterials

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          Abstract

          Fibroblast and macrophage are 2 dominant cell types respond cooperatively to degrade implanted biomaterials. Using an electrospun Dextran/Poly-lactide-co-glycolide (PLGA) scaffold as a model, an in vitro fibroblast/macrophage co-culture system was developed to investigate the degradability of implantable biodegradable materials. SEM showed that both fibroblasts and macrophages were able to degrade the scaffold, separately or cooperatively. Under the synergistic coordination of macrophages and fibroblasts, scaffolds showed faster degradation rate than their counterparts incubated with a single type of cells as well as in PBS or cell culture medium. Lysozyme, non-specific esterase (NSE), gelatinase, hyaluronidase-1 and alpha-glucosidase were up-regulated in the presence of the scaffold, suggesting their roles in the cell-mediated scaffold degradation. In addition, the expressions of cell surface receptors CD204 and Toll like receptor 4 (TLR4) were elevated 1 week after cell seeding, implying that these receptors might be involved in scaffold degradation. The results of in vivo subdermal implantation of the scaffold further confirmed the biodegradability of the Dextran/PLGA scaffold. The fibroblast/macrophage co-culture model adequately mimicked the in vivo environment and could be further developed into an in vitro tool for initial biomaterial evaluation.

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          Author and article information

          Journal
          Biomaterials
          Biomaterials
          0142-9612
          0142-9612
          Apr 2008
          : 29
          : 11
          Affiliations
          [1 ] Department of Biomedical Engineering, T18-030 Health Sciences Center, State University of New York-Stony Brook, Stony Brook, NY 11794-8181, United States.
          Article
          S0142-9612(07)00991-X NIHMS41776
          10.1016/j.biomaterials.2007.12.005
          2270789
          18192003
          c1711060-ba52-4eaf-b988-4e3a7bc68745
          History

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