Evidence map›Paper›PMID 7504060›Full record

ArticleThe Journal of experimental medicine1993

A critical role for monocytes and CD14 in endotoxin-induced endothelial cell activation.

J Pugin, R J Ulevitch, P S Tobias

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.8field-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

28 citing papers in PubMed, 149 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

J PuginDepartment of Immunology, Scripps Research Institute, La Jolla, California 92037.
R J Ulevitch
P S Tobias
Scripps Research Institute · US

Funding

TLR activation of Rho GTPase regulated signaling pathwayP01GM037696 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI ULEVITCH, RICHARD J · 1987 to 2006
$9.0M
MOLECULAR PATHOLOGY OF LPS HOST PROTEIN COMPLEXESR01AI032021 · NIAID · SCRIPPS RESEARCH INSTITUTE · PI TOBIAS, PETER S · 1992 to 2001
$559k
NIAID NIH HHS AI-32021NIGMS NIH HHS GM-37696
6 · The paper itself

Abstract

Vascular endothelium activated by endotoxin (lipopolysaccharide [LPS]) and cytokines plays an important role in organ inflammation and blood leukocyte recruitment observed during sepsis. Endothelial cells can be activated by LPS directly, after its interaction with LPS-binding protein and soluble CD14 in plasma. LPS-LPS-binding protein complexes in blood also interact with monocytes and neutrophils bearing glycosyl-phosphatidylinositol (GPI) anchored membrane CD14 (mCD14), promoting the release of cytokines such as tumor necrosis factor and interleukin 1 (IL-1). These molecules, in turn, have the capacity to activate endothelial cells providing an indirect pathway for LPS-dependent endothelial cell activation. In this work, we address the relative importance of the direct and the indirect pathway of in vitro LPS-induced human umbilical vein endothelial cell (HUVEC) activation. Substituting whole blood for plasma resulted in a 1,000-fold enhancement of HUVEC sensitivity to LPS. Both blood- and plasma-dependent enhanced activation of HUVEC were blocked with an anti-CD14 monoclonal antibody. Blood from patients with paroxysmal nocturnal hemoglobinuria, whose cells lack mCD14 and other GPI anchored proteins, was unable to enhance LPS activation of HUVEC above the level observed with plasma alone. IL-10, an inhibitor of monocyte release of cytokines, decreased the blood-dependent enhancement of HUVEC activation by LPS. Blood adapted to small doses of LPS was also less efficient than nonadapted blood in producing this enhancement. Addition of purified mononuclear cells to HUVEC or the transfer of plasma from whole blood incubated with LPS to HUVEC, duplicated the enhancement effect observed when whole blood was incubated with HUVEC. Taken together, these data suggest that the indirect pathway of LPS activation of endothelial cell is mediated by monocytes and mCD14 through the secretion of a soluble mediator(s). The indirect pathway is far more efficient than the direct, plasma-dependent pathway.

Indexed as

Cell AdhesionAntigens, CDAntigens, Differentiation, MyelomonocyticCell Adhesion MoleculesEndothelium, VascularHemoglobinuria, ParoxysmalHumansInterleukin-10In Vitro TechniquesLipopolysaccharide ReceptorsLipopolysaccharidesMonocytesSolubilityUp-RegulationVascular Cell Adhesion Molecule-1Antigens, CDAntigens, Differentiation, MyelomonocyticCell Adhesion MoleculesInterleukin-10Lipopolysaccharide ReceptorsLipopolysaccharidesVascular Cell Adhesion Molecule-1

Identifiers

PMID7504060
PMCPMC2191301
OpenAlexW2109609116

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.