Evidence map›Paper›PMID 33479269›Full record

ArticleScientific reports2021

Tissue-specific endothelial cell heterogeneity contributes to unequal inflammatory responses.

Hasitha Gunawardana, Tahmineh Romero, Ning Yao, Sebastiaan Heidt, Arend Mulder, David A Elashoff, Nicole M Valenzuela

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.8field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Microenvironmental determinants of endothelial cell heterogeneity.Nature reviews. Molecular cell biology · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Immunomodulation by allograft endothelial cells.Frontiers in transplantation · 2025
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. The Transplant Bellwether: Endothelial Cells in Antibody-Mediated Rejection.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
  17. Article
  18. Article
  19. Review
  20. 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

7 authors at 2 institutions in 2 countries.

Hasitha GunawardanaDepartment of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California Los Angeles, 1000 Veteran Avenue, Room 1-520, Los Angeles, CA, 90095, USA.
Tahmineh RomeroStatistics Core, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
Ning YaoStatistics Core, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
Sebastiaan HeidtDepartment of Immunohaematology and Blood Transfusion, Leiden University Medical Center, Leiden, The Netherlands.
Arend MulderDepartment of Immunohaematology and Blood Transfusion, Leiden University Medical Center, Leiden, The Netherlands.
David A ElashoffStatistics Core, David Geffen School of Medicine, University of California, Los Angeles, CA, USA.
Nicole M ValenzuelaDepartment of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California Los Angeles, 1000 Veteran Avenue, Room 1-520, Los Angeles, CA, 90095, USA. npyburn@mednet.ucla.edu.
University of California, Los Angeles · USLeiden University Medical Center · NL

Funding

Pilot and Feasibility ProgramP30DK041301 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1990 to 2019
$18.0M
International Society for Heart and Lung Transplantation Norman E Shumway/Enduring Hearts Career Development AwardNIDDK NIH HHS P30 DK041301
6 · The paper itself

Abstract

Endothelial cells (EC) coordinate vascular homeostasis and inflammation. In organ transplantation, EC are a direct alloimmune target. We posited that tissue specific heterogeneity of vascular EC may partly underlie the disparate organ-specific alloimmune risk. We examined the vascular endothelial response to inflammation across six primary endothelial beds from four major transplanted organs: the heart, lung, kidney and liver. First, we reanalyzed a public dataset of cardiac allograft rejection and found that endothelial inflammatory response genes were elevated in human cardiac allograft biopsies undergoing rejection compared with stable grafts. Next, the inducible inflammatory phenotypes of EC from heart, lung, kidney, and liver were characterized in vitro, focused on expression of adhesion molecules and chemokines, and recruitment of allogeneic peripheral blood mononuclear immune cells. Large vessel cardiac EC most highly upregulated VCAM-1, particularly compared with hepatic EC, supported greater leukocyte adhesion and had distinct chemokine profiles after stimulation with cytokines and complement. Differentially expressed gene candidates that are known regulators of cytokine signaling and inflammatory programming were verified in publicly available datasets of organ-specific endothelial transcriptomes. In summary, differential baseline expression of immune regulating genes may contribute to differential vascular inflammatory responses depending on organ.

Indexed as

AntibodiesBiomarkersCell Adhesion MoleculesChemokinesCytokinesEndothelial CellsEndothelium, VascularGraft RejectionHeart TransplantationHLA AntigensHumansInflammationAntibodiesBiomarkersCell Adhesion MoleculesChemokinesCytokinesHLA Antigens

Identifiers

PMID33479269
PMCPMC7820348
OpenAlexW3122274737

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.