4.8 Review

Challenges and strategies for in situ endothelialization and long-term lumen patency of vascular grafts

Journal

BIOACTIVE MATERIALS
Volume 6, Issue 6, Pages 1791-1809

Publisher

KEAI PUBLISHING LTD
DOI: 10.1016/j.bioactmat.2020.11.028

Keywords

Vascular graft; In situ endothelialization; Thrombogenesis; Intimal hyperplasia; Immunomodulation

Funding

  1. National Natural Science Foundation of China [82072396, 81871490, 81571022]
  2. Shanghai Collaborative Innovation Center for Translational Medicine [TM202010]
  3. Program of Shanghai Academic/Technology Research Leader [19XD1434500]
  4. Double Hundred Plan [20191819]
  5. Research Fund of Medicine and Engineering of Shanghai Jiao Tong University [YG2017MS06]

Ask authors/readers for more resources

Vascular diseases are a common cause of tissue necrosis, and vascular regeneration or artificial vascular grafts are conventional treatments that aim to improve long-term lumen patency. Strategies such as recruitment of EPCs, adhesion, proliferation and activation of EPCs and ECs, anti-thrombogenesis, anti-IH, and immunomodulation are important for enhancing the efficacy of vascular grafts.
Vascular diseases are the most prevalent cause of ischemic necrosis of tissue and organ, which even result in dysfunction and death. Vascular regeneration or artificial vascular graft, as the conventional treatment modality, has received keen attentions. However, small-diameter (diameter < 4 mm) vascular grafts have a high risk of thrombosis and intimal hyperplasia (IH), which makes long-term lumen patency challengeable. Endothelial cells (ECs) form the inner endothelium layer, and are crucial for anti-coagulation and thrombogenesis. Thus, promoting in situ endothelialization in vascular graft remodeling takes top priority, which requires recruitment of endothelia progenitor cells (EPCs), migration, adhesion, proliferation and activation of EPCs and ECs. Chemotaxis aimed at ligands on EPC surface can be utilized for EPC homing, while nanofibrous structure, biocompatible surface and cell-capturing molecules on graft surface can be applied for cell adhesion. Moreover, cell orientation can be regulated by topography of scaffold, and cell bioactivity can be modulated by growth factors and therapeutic genes. Additionally, surface modification can also reduce thrombogenesis, and some drug release can inhibit IH. Considering the influence of macrophages on ECs and smooth muscle cells (SMCs), scaffolds loaded with drugs that can promote M2 polarization are alternative strategies. In conclusion, the advanced strategies for enhanced long-term lumen patency of vascular grafts are summarized in this review. Strategies for recruitment of EPCs, adhesion, proliferation and activation of EPCs and ECs, anti-thrombogenesis, anti-IH, and immunomodulation are discussed. Ideal vascular grafts with appropriate surface modification, loading and fabrication strategies are required in further studies.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available