Evidence map›Paper›PMID 40724816›Full record

ArticleInternational journal of molecular sciences2025

Effect of Platelet-Derived Microparticles on the Expression of Adhesion Molecules in Endothelial Cells.

Elvira Varela-López, Socorro Pina-Canseco, Felipe Massó-Rojas, Claudia Lerma, Ana María Mejía Domínguez, Jesús Oswaldo García Ávila, Juan Carlos Torres-Narváez, Alvaro Vargas-González, Araceli Páez-Arenas

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Vitamin D and Kawasaki disease.Frontiers in pharmacology · 2026
    Review
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.

Elvira Varela-LópezLaboratorio de Medicina Traslacional, Unidad de Investigación UNAM-INC, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City 04480, Mexico.ORCID 0000-0001-5324-4664
Socorro Pina-CansecoCentro de Investigación, Facultad de Medicina-UNAM-UABJO, Universidad Autónoma "Benito Juárez" de Oaxaca, Oaxaca 68020, Mexico.ORCID 0000-0002-9486-5093
Felipe Massó-RojasLaboratorio de Medicina Traslacional, Unidad de Investigación UNAM-INC, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City 04480, Mexico.ORCID 0000-0001-8671-3367
Claudia LermaDepartamento de Biología Molecular, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City 04480, Mexico.ORCID 0000-0002-4679-7751
Ana María Mejía DomínguezBanco de Sangre, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City 14080, Mexico.
Jesús Oswaldo García ÁvilaHIV/STI Prevention Department, Fort Bend Country Health Department, Richmond, VA 77469, USA.
Juan Carlos Torres-NarváezDepartamento de Farmacología, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City 04480, Mexico.ORCID 0000-0002-3669-7482
Alvaro Vargas-GonzálezDepartamento de Fisiología, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City 04480, Mexico.ORCID 0000-0001-8189-2503
Araceli Páez-ArenasLaboratorio de Medicina Traslacional, Unidad de Investigación UNAM-INC, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City 04480, Mexico.ORCID 0000-0003-4688-8271

Funding

the Instituto Nacional de Cardiología Ignacio Chávez 22-1343
6 · The paper itself

Abstract

In healthy conditions and cardiovascular diseases, the most abundant microparticles (MPs) in the bloodstream are those of platelet origin, but the direct effect of these microparticles on endothelial activation is poorly understood. The objective of this paper is to measure endothelial cell activation, as evaluated by the expression of the adhesion molecules E-selectin, VCAM-1, ICAM-1, and PECAM-1 in endothelial cell line HMEC-1 when stimulated with MPs produced by platelets stimulated in vitro with thrombin (TH), adenosine diphosphate (ADP), calcium ionophore (ICa), N-acetylglucosamine (NAcGlc), and without any stimulus. Platelets from healthy individuals induced the formation of MPs with different agonists. The results from the determination of the phenotype of the MPs showed that the expression of GPIIb/IIIa was significant, with median fold changes of TH = 2.2, ADP = 5.2, Ica = 7.0, and NAcGlc = 10.0. However, in HMEC-1 cells, the expression of adhesion molecules stimulated with MPs had a median change slightly higher for E-Sel expression (ranging from 1.4 to 4.2) and ICAM-1 expression (range 2.2 to 3.0), especially VCAM-1 expression (ranging from 15 to 18.8), all of which were significant. For PECAM-1, only stimulation with ICa (1.5) was significant, demonstrating that MPs elicit stimulus-dependent responses in endothelial cells. Platelet-derived MPs may have a potential role in modulating inflammation and other endothelial functions.

Indexed as

Blood PlateletsCell Adhesion MoleculesCell-Derived MicroparticlesEndothelial CellsCell LineE-SelectinHumansIntercellular Adhesion Molecule-1Platelet Endothelial Cell Adhesion Molecule-1Vascular Cell Adhesion Molecule-1Cell Adhesion MoleculesE-SelectinIntercellular Adhesion Molecule-1Platelet Endothelial Cell Adhesion Molecule-1Vascular Cell Adhesion Molecule-1adhesion moleculesendothelial cellsmicroparticlesplatelets

Identifiers

PMID40724816
PMCPMC12294387

What OpenQuestion holds

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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.