2009
DOI: 10.1016/j.biomaterials.2009.08.054
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Engineering human neo-tendon tissue in vitro with human dermal fibroblasts under static mechanical strain

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Cited by 123 publications
(111 citation statements)
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“…Porcine dermal fibroblasts and TCs loaded on PLGA electro-spun fibres have been shown to promote tenogenic function in vitro and improved healing, as evidenced by improved gross morphology, histological analysis and biomechanical properties, in vivo [413][414][415][416]. In conjugation with BMSCs, electro-spun PLGA scaffolds have demonstrated suppression of lymphocytes in vitro and improved biomechanical properties and acceptable integration into the native tendon tissue [417].…”
Section: Bottom-up Approached For Tendon Repair Based On Synthetic Inmentioning
confidence: 99%
“…Porcine dermal fibroblasts and TCs loaded on PLGA electro-spun fibres have been shown to promote tenogenic function in vitro and improved healing, as evidenced by improved gross morphology, histological analysis and biomechanical properties, in vivo [413][414][415][416]. In conjugation with BMSCs, electro-spun PLGA scaffolds have demonstrated suppression of lymphocytes in vitro and improved biomechanical properties and acceptable integration into the native tendon tissue [417].…”
Section: Bottom-up Approached For Tendon Repair Based On Synthetic Inmentioning
confidence: 99%
“…39,40 As shown in Figure 6, TEM examination revealed that the collagen fibrils remained immature (the diameter was small and the arrangement was random), mostly because the scaffold needs a longer culture time in vivo and more cyclic mechanical training. 40,41 The mechanical strength of the scaffold plays an important role in reconstructing abdominal wall defects, which can be used to predict the success or failure of the surgery. The mechanical strength provided by the scaffold, can be divided into two parts: the collagen fibrils of the SIS before degradation and the neo-tissue after implantation.…”
mentioning
confidence: 99%
“…2 Unfortunately, the clinical application of ESCs is restricted due to their limited availability (depending on the policy of different countries) and the complexity of cell manipulation required. Dermal fibroblasts have also been shown to form tendon tissue, [30][31][32] although further research has suggested that the healing process using skin-derived fibroblasts is suppressed with a lack of tenocyte markers and histopathologic correlations. 33,34 Being native cell sources, tenocytes and in situ fibroblasts are perhaps the most ideal cell sources for engineered tendon and ligament tissue, respectively.…”
Section: Introductionmentioning
confidence: 99%