Proangiogenic microtemplated fibrin scaffolds containing aprotinin promote improved wound healing responses

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• 作者：Kassandra S. Thomson (1) (2)
  Sarah K. Dupras (2)
  Charles E. Murry (1) (2) (3)
  Marta Scatena (1) (2)
  Michael Regnier (1) (2)
  
• 关键词：Aprotinin ; Fibrin ; Scaffold implant ; Angiogenic response ; Wound healing
• 刊名：Angiogenesis
• 出版年：2014
• 出版时间：January 2014
• 年：2014
• 卷：17
• 期：1
• 页码：195-205
• 全文大小：1,999 KB
• 作者单位：Kassandra S. Thomson (1) (2)
  Sarah K. Dupras (2)
  Charles E. Murry (1) (2) (3)
  Marta Scatena (1) (2)
  Michael Regnier (1) (2)
  
  1. Department of Bioengineering, University of Washington, Seattle, WA, 98195-5061, USA
  2. Center for Cardiovascular Biology, Institute for Stem Cell and Regenerative Medicine, University of Washington, School of Medicine, Seattle, WA, 98195-8050, USA
  3. Departments of Pathology and Medicine/Cardiology, University of Washington, Seattle, WA, 98109, USA
  
• ISSN：1573-7209

文摘

Survival of tissue engineered constructs after implantation depends heavily on induction of a vascular response in host tissue, promoting a quick anastomosis of the cellular graft. Additionally, implanted constructs typically induce fibrous capsule formation, effectively preventing graft integration with host tissue. Previously we described the development of a high density microtemplated fibrin scaffold for cardiac tissue engineering applications with tunable degradation and mechanical properties which promoted seeded cell survival and organization in vitro (Thomson et al., Tissue Eng Part A, 2013). Scaffold degradation in vitro was controllable by addition of the serine protease inhibitor aprotinin and/or the fibrin cross-linker Factor XIII (FXIII). The goal of this study was to assess host tissue responses to these fibrin scaffold formulations by determining effects on scaffold degradation, angiogenic responses, and fibrous capsule formation in a subcutaneous implant model. Aprotinin significantly decreased scaffold degradation over 2?weeks of implantation. A significant increase in capillary infiltration of aprotinin implants was found after 1 and 2?weeks, with a significantly greater amount of capillaries reaching the interior of aprotinin scaffolds. Interestingly, after 2?weeks the aprotinin scaffolds had a significantly thinner, yet apparently more cellular fibrous capsule than unmodified scaffolds. These results indicate aprotinin not only inhibits fibrin scaffold degradation, but also induces significant responses in the host tissue. These included an angiogenic response resulting in increased vascularization of the scaffold material over a relatively short period of time. In addition, aprotinin release from scaffolds may reduce fibrous capsule formation, which could help promote improved integration of cell-seeded scaffolds with host tissue.