Evidence map›Paper›PMID 27936727›Full record

ArticleBiomacromolecules2016

Targeting Heparin to Collagen within Extracellular Matrix Significantly Reduces Thrombogenicity and Improves Endothelialization of Decellularized Tissues.

Bin Jiang, Rachel Suen, Jason A Wertheim, Guillermo A Ameer

Open access · greenAbstract read
In one paragraph

Article in Biomacromolecules, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Recent Advances in Liver Engineering With Decellularized Scaffold.Frontiers in bioengineering and biotechnology · 2022
    Review
  9. Article
  10. Article
  11. Review
  12. Extracellular matrix grafts: From preparation to application (Review).International journal of molecular medicine · 2021
    Review
  13. Article
  14. Review
  15. Review
  16. Vascularization in tissue engineering: fundamentals and state-of-art.Progress in biomedical engineering (Bristol, England) · 2020
    Article
  17. Article
  18. Article
  19. 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

4 authors at 1 institution in 1 country.

Bin JiangDepartment of Surgery, Feinberg School of Medicine, Northwestern University , Chicago, Illinois 60611, United States.
Rachel Suen
Jason A WertheimDepartment of Surgery, Feinberg School of Medicine, Northwestern University , Chicago, Illinois 60611, United States.
Guillermo A AmeerDepartment of Surgery, Feinberg School of Medicine, Northwestern University , Chicago, Illinois 60611, United States.
Northwestern University · US

Funding

Preclinical Investigation of a Bioengineered Vascular GraftR01EB017129 · NIBIB · NORTHWESTERN UNIVERSITY · PI AMEER, GUILLERMO ANTONIO, KIBBE, MELINA RAE · 2013 to 2016
$1.8M
Optimization and control of hepatocyte activity via biofunctional modificationK08DK101757 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WERTHEIM, JASON A · 2014 to 2018
$777k
NIBIB NIH HHS R01 EB017129NIDDK NIH HHS K08 DK101757
6 · The paper itself

Abstract

Thrombosis within small-diameter vascular grafts limits the development of bioartificial, engineered vascular conduits, especially those derived from extracellular matrix (ECM). Here we describe an easy-to-implement strategy to chemically modify vascular ECM by covalently linking a collagen binding peptide (CBP) to heparin to form a heparin derivative (CBP-heparin) that selectively binds a subset of collagens. Modification of ECM with CBP-heparin leads to increased deposition of functional heparin (by ∼7.2-fold measured by glycosaminoglycan composition) and a corresponding reduction in platelet binding (>70%) and whole blood clotting (>80%) onto the ECM. Furthermore, addition of CBP-heparin to the ECM stabilizes long-term endothelial cell attachment to the lumen of ECM-derived vascular conduits, potentially through recruitment of heparin-binding growth factors that ultimately improve the durability of endothelialization in vitro. Overall, our findings provide a simple yet effective method to increase deposition of functional heparin on the surface of ECM-based vascular grafts and thereby minimize thrombogenicity of decellularized tissue, overcoming a significant challenge in tissue engineering of bioartificial vessels and vascularized organs.

Indexed as

AnimalsCoated Materials, BiocompatibleCollagenExtracellular MatrixHeparinHumansHuman Umbilical Vein Endothelial CellsMalePeptide FragmentsPlatelet AdhesivenessRatsRats, Sprague-DawleyThrombosisTissue EngineeringTissue ScaffoldsCoated Materials, BiocompatibleCollagenHeparinPeptide Fragments

Identifiers

PMID27936727
PMCPMC5274546
OpenAlexW2547754829

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.