107 Enhanced endothelial cell coverage on graphene coated stents

Author(s):  
Fatemeh Jafarzadeh ◽  
Daryl McManus ◽  
Irina Barbolina ◽  
Kostas Kostarelos ◽  
Nadim Malik ◽  
...  
2012 ◽  
Vol 8 (9) ◽  
pp. 3509-3515 ◽  
Author(s):  
S.M. Derkaoui ◽  
A. Labbé ◽  
P. Chevallier ◽  
S. Holvoet ◽  
C. Roques ◽  
...  

2020 ◽  
pp. neurintsurg-2020-016859
Author(s):  
Alyssa McCulloch ◽  
Ashley Turcott ◽  
Gabriella Graham ◽  
Sergey Frenklakh ◽  
Kristen O'Halloran Cardinal

ObjectiveThe goal of this work was to endothelialize silicone aneurysm tubes for use as in vitro models for evaluating endothelial cell interactions with neurovascular devices. The first objective was to establish consistent and confluent endothelial cell linings and to evaluate the silicone vessels over time. The second objective was to use these silicone vessels for flow diverter implantation and assessment.MethodsSilicone aneurysm tubes were coated with fibronectin and placed into individual bioreactor systems. Human umbilical vein endothelial cells were deposited within tubes to create silicone vessels, then cultivated on a peristaltic pump and harvested at 2, 5, 7, or 10 days to evaluate the endothelial cell lining. A subset of silicone aneurysm vessels was used for flow diverter implantation, and evaluated for cell coverage over device struts at 3 or 7 days after deployment.ResultsSilicone vessels maintained confluent, PECAM-1 (platelet endothelial cell adhesion molecule 1) positive endothelial cell linings over time. These vessels facilitated and withstood flow diverter implantation, with robust cell linings disclosed after device deployment. Additionally, the endothelial cells responded to implanted devices through coverage of the flow diverter struts with increased cell coverage over the aneurysm seen at 7 days after deployment as compared with 3 days.ConclusionsSilicone aneurysm models can be endothelialized and successfully maintained in vitro over time. Furthermore, these silicone vessels can be used for flow diverter implantation and assessment.


1995 ◽  
Vol 58 (1) ◽  
pp. 58-68 ◽  
Author(s):  
David A. Bull ◽  
Glenn C. Hunter ◽  
Hana Holubec ◽  
Maria L. Aguirre ◽  
William D. Rappaport ◽  
...  

2019 ◽  
Vol 12 (3) ◽  
pp. 566-567
Author(s):  
Sho Torii ◽  
Maria E. Romero ◽  
Frank D. Kolodgie ◽  
Aloke V. Finn ◽  
Renu Virmani

2017 ◽  
Vol 204 (3-4) ◽  
pp. 199-209 ◽  
Author(s):  
Alexandru Mogaldea ◽  
Tobias Goecke ◽  
Karolina Theodoridis ◽  
Axel Haverich ◽  
Serghei Cebotari ◽  
...  

Valvular repair or transplantation, designed to restore the venous valve function of the legs, has been proposed as treatment in chronic venous insufficiency. Available grafts or surgeries have provided limited durability so far. Generating venous valve substitutes by means of tissue engineering could be a solution. We generated decellularized jugular ovine vein conduits containing valves (oVVC) after reseeding with ovine endothelial cells differentiated from peripheral blood-derived endothelial cells (oPBEC), cultivated in vitro corresponding to the circulatory situation in the lower leg at rest and under exertion. oVVC were decellularized by detergent treatment. GFP-labeled oPBEC were seeded onto the luminal side of the decellularized oVVC and cultivated under static-rotational conditions for 6 h (group I) and 12 h (group II), respectively. Reseeded matrices of group I were exposed to continuous low flow conditions (“leg at rest”). The tissues of group II were exposed to a gradually increasing flow (“leg under effort”). After 5 days, the grafts of group I revealed a uniform luminal endothelial cell coverage of the examined areas of the venous walls and adjacent venous valve leaflets. In group II, the cell coverage on luminal areas of the venous wall parts was found to be nearly complete. The endothelial cell coverage of adjacent venous valve leaflets was revealed to be less dense and confluent. Endothelial cells cultured on acellular vein tissues of both groups were distinctly orientated uniformly in the flow direction, clearly creating a stable and flow-orientated layer. Thus, an endothelium could successfully be reestablished on the luminal surface of a decellularized venous valve by seeding peripheral blood endothelial cells and culturing under different conditions.


2010 ◽  
Vol 6 (5) ◽  
pp. 630-637 ◽  
Author(s):  
Nicole Soucy ◽  
Julia Feygin ◽  
Radhika Tunstall ◽  
Melissa Casey ◽  
Douglas Pennington ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document