Evidence map›Paper›PMID 21657213›Full record

ArticleLangmuir : the ACS journal of surfaces and colloids2011

Using microcontact printing of fibrinogen to control surface-induced platelet adhesion and activation.

Lindsey E Corum, Colin D Eichinger, Tony W Hsiao, Vladimir Hlady

Abstract read
In one paragraph

Article in Langmuir : the ACS journal of surfaces and colloids, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

16 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. RGDfK-functionalized gold nanorods bind only to activated platelets.Journal of biomedical materials research. Part A · 2017
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Microfluidics and coagulation biology.Annual review of biomedical engineering · 2013
    Review
  13. Article
  14. Article
  15. Multiprotein microcontact printing with micrometer resolution.Langmuir : the ACS journal of surfaces and colloids · 2012
    Article
  16. 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.

Lindsey E CorumDepartment of Bioengineering, University of Utah, 20 South 2030 East, Salt Lake City, Utah 84112, USA.
Colin D Eichinger
Tony W Hsiao
Vladimir Hlady
University of Utah · US

Funding

SCREENING PLATELETS INTERACTIONS WITH SURFACE GRADIENTSR01HL084586 · NHLBI · UNIVERSITY OF UTAH · PI HLADY, VLADIMIR · 2006 to 2009
$877k
NHLBI NIH HHS 5R01 HL84586NHLBI NIH HHS R01 HL084586
6 · The paper itself

Abstract

The ability to promote or inhibit specific platelet-surface interactions in well-controlled environments is crucial to studying fundamental adhesion and activation mechanisms. Here, microcontact printing was used to immobilize human fibrinogen covalently in the form of randomly placed, micrometer-sized islands at an overall surface coverage of 20, 50, or 85%. The nonprinted background region was blocked with covalently immobilized human albumin. Platelet adhesion and morphology on each substrate were assessed using combined differential interference and fluorescence microscopy. At 20% coverage, most of the fibrinogen surface features were small round islands, and platelet adhesion and spreading areas were limited by the position and the size of the islands. Platelet circularity, indicated the morphology was mostly rounded. At 50% coverage, some fibrinogen islands coalesced and platelet adhesion and spreading areas increased. Platelet morphology was controlled by the shape of underlying fibrinogen islands, leading to more irregular spreading. At 85% coverage, the fibrinogen pattern was completely interconnected and both platelet adhesion and the spreading area were significantly higher than at lower coverage. In addition, platelets also spread over the albumin regions, suggesting that after a critical surface density of fibrinogen ligands is reached, platelet spreading is no longer inhibited by albumin. Increasing the overall fibrinogen coverage resulted in higher activation levels defined by key morphological characteristics of the spreading platelet.

Indexed as

FibrinogenHumansParticle SizePlatelet ActivationPlatelet AdhesivenessSurface PropertiesFibrinogen

Identifiers

PMID21657213
PMCPMC3261074
OpenAlexW2025957525

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.