Evidence map›Paper›PMID 37027378›Full record

ArticlePloS one2023

Fluorescent microspheres can affect in vitro fibrinolytic outcomes.

Ethan G Stoll, Sean J Cone, Spencer R Lynch, Andrew T Fuquay, Brittany E Bannish, Nathan E Hudson

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Deconstructing fibrin(ogen) structure.Journal of thrombosis and haemostasis : JTH · 2025
    Review
  2. Article
  3. 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

6 authors at 4 institutions in 1 country.

Ethan G StollDept. Physics, East Carolina University, Greenville, North Carolina, United States of America.
Sean J ConeDepartment of Biological Sciences, North Carolina State University, Raleigh, North Carolina, United States of America.
Spencer R LynchMedical Physics Graduate Program, Duke University, Durham, North Carolina, United States of America.ORCID 0000-0002-1172-275X
Andrew T FuquayMedical Physics Graduate Program, Duke University, Durham, North Carolina, United States of America.
Brittany E BannishDept. Mathematics and Statistics, University of Central Oklahoma, Edmond, Oklahoma, United States of America.
Nathan E HudsonDept. Physics, East Carolina University, Greenville, North Carolina, United States of America.ORCID 0000-0003-0573-7661
Duke University · USEast Carolina University · USNorth Carolina State University · USUniversity of Central Oklahoma · US

Funding

Identifying the function of the Fibrin(ogen) alpha-C connector regionR15HL148842 · NHLBI · EAST CAROLINA UNIVERSITY · PI HUDSON, NATHAN · 2019 to 2024
$893k
NHLBI NIH HHS R15 HL148842
6 · The paper itself

Abstract

Hemostasis is the cessation of bleeding due to the formation of a blood clot. After the completion of wound healing, the blood clot is typically dissolved through the natural process of fibrinolysis, the enzymatic digestion by plasmin of the fibrin fibers that make up its structural scaffold. In vitro studies of fibrinolysis reveal mechanisms regulating these processes and often employ fluorescent microscopy to observe protein colocalization and fibrin digestion. In this study, we investigate the effects of labeling a fibrin network with 20 nm diameter fluorescent beads (fluorospheres) for the purpose of studying fibrinolysis. We observed fibers and 2-D fibrin networks labeled with fluorospheres during fibrinolysis. We found that the labeling of fibrin with fluorospheres can alter fibrinolytic mechanisms. In previous work, we showed that, during lysis, fibrin fibers are cleaved into two segments at a single location. Herein we demonstrate that fibrinolysis can be altered by the concentration of fluorospheres used to label the fibers, with high concentrations of fluorospheres leading to very minimal cleaving. Furthermore, fibers that are left uncleaved after the addition of plasmin often elongate, losing their inherent tension throughout the imaging process. Elongation was especially prominent among fibers that had bundled together due to other cleavage events and was dependent on the concentration of fluorophores used to label fibers. Of the fibers that do cleave, the site at which they cleave also shows a predictable trend dependent on fluorosphere concentration; low concentrations heavily favor cleavage locations at either end of fibrin fiber and high concentrations show no disparity between the fiber ends and other locations along the fiber. After the initial cleavage event bead concentration also affects further digestion, as higher bead concentrations exhibited a larger population of fibers that did not digest further. The results described in this paper indicate that fluorescent labeling strategies can impact fibrinolysis results.

Indexed as

FibrinolysinThrombosisFibrinFibrinolysisHumansMicrospheresFibrinFibrinolysin

Identifiers

PMID37027378
PMCPMC10081780
OpenAlexW4362691874

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.