4.6 Article

Fabrication of New Hybrid Scaffolds for in vivo Perivascular Application to Treat Limb Ischemia

期刊

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcvm.2020.598890

关键词

tissue engineering; angiogenesis; adventitial pericytes; hybrid scaffold; biomaterials; bioprinting; electrospinning

资金

  1. BHF Ph.D. studentship [FS/15/7/31307]
  2. BHF project grant [PG/18/38/33707]
  3. NIHR Biomedical Research Centre at University Hospitals Bristol NHS Foundation Trust
  4. University of Bristol

向作者/读者索取更多资源

Cell therapies are emerging as a new therapeutic frontier for the treatment of ischemic disease. However, femoral occlusions can be challenging environments for effective therapeutic cell delivery. In this study, cell-engineered hybrid scaffolds are implanted around the occluded femoral artery and the therapeutic benefit through the formation of new collateral arteries is investigated. First, it is reported the fabrication of different hybrid hard-soft 3D channel-shaped scaffolds comprising either poly(epsilon-caprolactone) (PCL) or polylactic-co-glycolic acid (PLGA) and electro-spun of gelatin (GL) nanofibers. Both PCL-GL and PLGA-GL scaffolds show anisotropic characteristics in mechanical tests and PLGA displays a greater rigidity and faster degradability in wet conditions. The resulting constructs are engineered using human adventitial pericytes (APCs) and both exhibit excellent biocompatibility. The 3D environment also induces expressional changes in APCs, conferring a more pronounced proangiogenic secretory profile. Bioprinting of alginate-pluronic gel (AG/PL), containing APCs and endothelial cells, completes the hybrid scaffold providing accurate spatial organization of the delivered cells. The scaffolds implantation around the mice occluded femoral artery shows that bioengineered PLGA hybrid scaffold outperforms the PCL counterpart accelerating limb blood flow recovery through the formation arterioles with diameters >50 mu m, demonstrating the therapeutic potential in stimulating reparative angiogenesis.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据