4.8 Article

Endothelial Cell-Mediated Gene Delivery for In Situ Accelerated Endothelialization of a Vascular Graft

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 14, Pages 16097-16105

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c01869

Keywords

matrix metalloproteinase; enzymatic responsivity; surface gene delivery; rapid endothelialization; peptide

Funding

  1. National Key R&D Program of China [2016YFC1100300]
  2. National Natural Science Foundation of China [51873149, 91939112, 51673145]

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The intelligent gene delivery small-caliber vascular graft combines EC adhesive peptide and responsive gene delivery system to achieve rapid endothelialization with high transfection efficiency. The gene release system on the graft surface undergoes enzymatic release, while also specifically adhering to ECs and maintaining temporary stability in blood flow due to the GPQGIWGQ-C peptide linker.
As an urgently needed device for vascular diseases, the small-diameter vascular graft is limited by high thrombogenicity in clinical applications. Rapid endothelialization is a promising approach to construct an antithrombogenic inner surface of the vascular graft. The main bottleneck for rapid endothelialization is the adhesion, migration, and proliferation of endothelial cells (ECs) in situ of the small-diameter vascular graft. Herein, we innovatively fabricated an intelligent gene delivery small-caliber vascular graft based on electrospun poly(lactic acid-co-caprolactone) and gelatin for rapid in situ endothelialization. The graft surface was co-modified with EC adhesive peptide of Arg-Glu-Asp-Val (REDV) and responsive gene delivery system. REDV can selectively adhere ECs onto the graft surface; subsequently, the overexpressed matrix metalloproteinase by ECs can effectively cleave the linker peptide GPQGIWGQ-C; and finally, the gene complexes were intelligently and enzymatically released from the graft surface, and thereby, the gene can efficiently transfect ECs. Importantly, this enzymatically releasing gene surface has been proven to be safe and temporarily stable in blood flow owing to the biotin-avidin interaction to immobilize gene complexes on the inner surface of vascular grafts through the GPQGIWGQ-C peptide linker. It has the advantage of specifically adhering the ECs to the surface and smartly transfecting them with high transfection efficiency. The co-modified surface has been demonstrated to accelerate the luminal endothelialization in vivo, which might be attributed to the synergistic effect of REDV and effective gene transfection. Particularly, the intelligent and responsive gene release surface will open a new avenue to enhance the endothelialization of blood-contacting devices.

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