46
IRUS Total
Downloads
  Altmetric

Endothelial repair in stented arteries is accelerated by inhibition of Rho-associated protein kinase.

File Description SizeFormat 
cvw210.pdfPublished version2.21 MBAdobe PDFView/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