Perivascular CLICK‐gelatin delivery of thrombospondin‐2 small interfering RNA decreases development of intimal hyperplasia after arterial injury

Author:

Mota Lucas1ORCID,Zhu Max1ORCID,Li Jennifer1ORCID,Contreras Mauricio1ORCID,Aridi Tarek1ORCID,Tomeo John N.1ORCID,Stafford Alexander2ORCID,Mooney David J.2ORCID,Pradhan‐Nabzdyk Leena1ORCID,Ferran Christiane134ORCID,LoGerfo Frank W.1ORCID,Liang Patric1ORCID

Affiliation:

1. Division of Vascular and Endovascular Surgery Beth Israel Deaconess Medical Center Boston Massachusetts USA

2. John A. Paulson School of Engineering and Applied Science Harvard University Cambridge Massachusetts USA

3. The Center for Vascular Biology Research Beth Israel Deaconess Medical Center Boston Massachusetts USA

4. Division of Nephrology, Department of Medicine Beth Israel Deaconess Medical Center Boston Massachusetts USA

Abstract

AbstractBypass graft failure occurs in 20%–50% of coronary and lower extremity bypasses within the first‐year due to intimal hyperplasia (IH). TSP‐2 is a key regulatory protein that has been implicated in the development of IH following vessel injury. In this study, we developed a biodegradable CLICK‐chemistry gelatin‐based hydrogel to achieve sustained perivascular delivery of TSP‐2 siRNA to rat carotid arteries following endothelial denudation injury. At 21 days, perivascular application of TSP‐2 siRNA embedded hydrogels significantly downregulated TSP‐2 gene expression, cellular proliferation, as well as other associated mediators of IH including MMP‐9 and VEGF‐R2, ultimately resulting in a significant decrease in IH. Our data illustrates the ability of perivascular CLICK‐gelatin delivery of TSP‐2 siRNA to mitigate IH following arterial injury.

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

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