4.7 Article

Development of high resilience spiral wound suture-embedded gelatin/PCL/heparin nanofiber membrane scaffolds for tendon tissue engineering

期刊

出版社

ELSEVIER
DOI: 10.1016/j.ijbiomac.2022.09.001

关键词

Gelatin; Heparin; Tendon tissue engineering; Basic fibroblast growth factor; Scaffold; Nanofiber

资金

  1. Ministry of Science and Technology, Taiwan, ROC [MOST 109-2314-B-182-013-MY3]
  2. Chang Gung Memorial Hospital, Taiwan, ROC [CMRPD2J0111, CMRPD2J0112, CMRPD2J0113]
  3. Ramalingaswami Fellowship, Department of Biotechnology, India

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This study develops a spiral wound scaffold based on gelatin/PCL/heparin (GPH) nanofiber membranes for tendon tissue engineering. The scaffold provides both biological and physical cues for tendon regeneration, resulting in enhanced mechanical properties and neotendon tissue formation in vivo.
This study develops a spiral wound scaffold based on gelatin/PCL/heparin (GPH) nanofiber membranes for tendon tissue engineering. By embedding sutures in dual layers of aligned GPH nanofiber membranes, prepared from mixed electrospinning of gelatin and PCL/heparin solutions, we fabricate a high resilience scaffold intended for the high loading environment experienced by tendons. The basic fibroblast growth factor (bFGF) was anchored to GPH scaffold through bioaffinity between heparin and bFGF, aim to provide biological cues for maintenance of tenogenic phenotype. In addition, the aligned nanofiber morphology is expected to provide physical cues toward seeded tenocytes. With sustained release of bFGF, GPH-bFGF can enhance proliferation, upregulate tenogenic gene expression, and increase synthesis of tendon-specific proteins by tenocytes in vitro. Furthermore, by properly maintaining tendon phenotypes, GPH-bFGF/tenocytes constructs showed improved mechanical properties over GPH-bFGF. From in vivo study using GPH-bFGF/tenocytes constructs to repair rabbit Achilles tendon defects, neotendon tissue formation was confirmed from histological staining and biomechanical analysis. These findings collectively demonstrate that the newly designed GPH-bFGF scaffold could provide a niche for inducing tendon tissue regeneration by effectively restoring the tendon tissue structure and function.

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