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Endothelial repair in stented arteries is accelerated by inhibition of Rho-associated protein kinase.
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cvw210.pdf | Published version | 2.21 MB | Adobe PDF | View/Open |
Title: | Endothelial repair in stented arteries is accelerated by inhibition of Rho-associated protein kinase. |
Authors: | Hsiao, ST Spencer, T Boldock, L Prosseda, SD Xanthis, I Tovar-Lopez, FJ Van Buesekamp, H Khamis, RY Foin, N Bowden, N Hussain, A Rothman, A Ridger, V Halliday, I Perrault, C Gunn, J Evans, PC |
Item Type: | Journal Article |
Abstract: | AIMS: Stent deployment causes endothelial cell (EC) denudation, which promotes in-stent restenosis and thrombosis. Thus endothelial regrowth in stented arteries is an important therapeutic goal. Stent struts modify local hemodynamics, however the effects of flow pertubation on EC injury and repair are incompletely understood. By studying the effects of stent struts on flow and EC migration we identified an intervention that promotes endothelial repair in stented arteries. METHODS AND RESULTS: In vitro and in vivo models were developed to monitor endothelialization under flow and the influence of stent struts. A 2D parallel-plate flow chamber with 100 μm ridges arranged perpendicular to the flow was used. Live cell imaging coupled to computational fluid dynamic simulations revealed that EC migrate in the direction of flow upstream from the ridges but subsequently accumulate downstream from ridges at sites of bidirectional flow. The mechanism of EC trapping by bidirectional flow involved reduced migratory polarity associated with altered actin dynamics. Inhibition of Rho-associated protein kinase (ROCK) enhanced endothelialization of ridged surfaces by promoting migratory polarity under bidirectional flow (p<0.01). To more closely mimic the in vivo situation we cultured EC on the inner surface of polydimethylsiloxane tubing containing Coroflex Blue stents (65 μm struts) and monitored migration. ROCK inhibition significantly enhanced EC accumulation downstream from struts under flow (p<0.05). We investigated the effects of ROCK inhibition on re-endothelialization in vivo using a porcine model of EC denudation and stent placement. En face staining and confocal microscopy revealed that inhibition of ROCK using fasudil (30 mg/day via osmotic minipump) significantly increased re-endothelialization of stented carotid arteries (p<0.05). CONCLUSIONS: Stent struts delay endothelial repair by generating localised bidirectional flow which traps migrating EC. ROCK inhibitors accelerate endothelial repair of stented arteries by enhancing EC polarity and migration through regions of bidirectional flow. |
Issue Date: | 26-Sep-2016 |
Date of Acceptance: | 26-Sep-2016 |
URI: | http://hdl.handle.net/10044/1/42200 |
DOI: | https://dx.doi.org/10.1093/cvr/cvw210 |
ISSN: | 1755-3245 |
Publisher: | Oxford University Press (OUP) |
Start Page: | 689 |
End Page: | 701 |
Journal / Book Title: | Cardiovascular Research |
Volume: | 112 |
Issue: | 3 |
Copyright Statement: | © The Author 2016. Published by Oxford University Press on behalf of the European Society of Cardiology. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
Keywords: | Endothelial cells Fasudil ROCK Shear stress Stent Cardiovascular System & Hematology 1102 Cardiovascular Medicine And Haematology |
Publication Status: | Published |
Open Access location: | http://cardiovascres.oxfordjournals.org/content/early/2016/09/25/cvr.cvw210 |
Appears in Collections: | National Heart and Lung Institute |