Evidence map›Paper›PMID 24952977›Full record

ArticleBiomaterials2014

Endothelial retention and phenotype on carbonized cardiovascular implant surfaces.

Christopher M Frendl, Scott M Tucker, Nadeem A Khan, Mandy B Esch, Shrinidhi Kanduru, Thong M Cao, Andrés J García, Michael R King, Jonathan T Butcher

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.2field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 23 citations in OpenAlex.

  1. Triple Helical-Peptides: Collagen-Mimicking Tools for Tissue Engineering.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Christopher M FrendlDepartment of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Scott M TuckerDepartment of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Nadeem A KhanDepartment of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Mandy B EschDepartment of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Shrinidhi KanduruDepartment of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Thong M CaoDepartment of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Andrés J GarcíaWoodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA, USA.
Michael R KingDepartment of Biomedical Engineering, Cornell University, Ithaca, NY, USA.
Jonathan T ButcherDepartment of Biomedical Engineering, Cornell University, Ithaca, NY, USA. Electronic address: jtb47@cornell.edu.
Cornell University · USGeorgia Institute of Technology · US

Funding

Osseo-reparative, integrin-specific materialsR01AR062920 · NIAMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI GARCIA, ANDRES J · 2012 to 2021
$3.2M
Model of Platelet Adhesion and Thrombus FormationR01HL097971 · NHLBI · CORNELL UNIVERSITY · PI DIACOVO, THOMAS G, KING, MICHAEL R. · 2010 to 2014
$2.0M
Biomechanical regulation of valvulogenesisR01HL110328 · NHLBI · CORNELL UNIVERSITY · PI BUTCHER, JONATHAN TALBOT · 2011 to 2015
$1.9M
Effects of hydroxyapatite mineralization and valve cell phenotypeR21HL118672 · NHLBI · CORNELL UNIVERSITY · PI BUTCHER, JONATHAN TALBOT · 2013 to 2014
$405k
NHLBI NIH HHS R01 HL097971NHLBI NIH HHS R01 HL110328NHLBI NIH HHS R21 HL118672NIAMS NIH HHS R01 AR062920
6 · The paper itself

Abstract

Heart valve disease is an increasing clinical burden for which there is no effective treatment outside of prosthetic replacement. Over the last 20 years, clinicians have increasingly preferred the use of biological prosthetics to mechanical valves despite their superior durability because of the lifelong anticoagulation therapy that is required. Mechanical valve surface engineering has largely focused on being as non-thrombogenic as possible, but despite decades of iteration has had insufficient impact on the anticoagulation burden. In this study, we systematically evaluate the potential for endothelialization of the pyrolytic carbon surface used in mechanical valves. We compared adsorbed adhesion ligand type (collagen I, fibronectin, laminin, and purified adhesion domain fragments GFOGER and FN7-10) and concentration on endothelial adhesion rates and adhesion strength on Medtronic-Hall prosthetic valve surfaces. Regardless of ligand type or concentration, endothelial adhesion strengthening was insufficient for their intended ultra-high shear stress environment. We then hypothesized that microfabricated trenches would reduce shear stress to tolerable levels while maintaining endothelial access to the flow stream, thereby promoting a confluent and anticoagulant endothelial monolayer. Computational fluid dynamics simulations predicted an empirical relationship of channel width, depth, and spacing that would maintain interior surface shear stress within tolerable levels. Endothelial cells seeded to confluence in these channels retained a confluent monolayer when exposed to 600 dyn/cm(2) shear stress for 48 h regardless of applied adhesive ligand. Furthermore, sheared EC expressed a mature anti-coagulant profile, including endothelial nitric oxide synthase (eNOS), VE-cadherin, and significantly downregulated plasminogen activator inhibitor-1 (PAI-1). As a final test, channeled pyrolytic carbon surfaces with confluent EC reduced human platelet adhesion 1000-fold over pyrolytic carbon alone. These results advance a promising biohybrid approach to enable active moderation of local coagulative response in mechanical heart valves, which could significantly extend the utility of this important treatment for heart valve disease.

Indexed as

Blood Vessel ProsthesisImplants, ExperimentalAdsorptionAnimalsCarbonCell AdhesionCoagulantsEndothelial CellsHumansHydrodynamicsLigandsMicrofluidicsPhenotypePlatelet AdhesivenessProteinsSiliconCarbonCoagulantsLigandsProteinsSiliconAdhesion peptideComputational fluid dynamicsHemodynamicsHemostasisMechanical heart valvesPlatelet adhesion

Identifiers

PMID24952977
PMCPMC4442700
OpenAlexW2034702985

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.