Evidence map›Paper›PMID 28754719›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2017

Visualization of three pathways for macromolecule transport across cultured endothelium and their modification by flow.

Mean Ghim, Paola Alpresa, Sung-Wook Yang, Sietse T Braakman, Stephen G Gray, Spencer J Sherwin, Maarten van Reeuwijk, Peter D Weinberg

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.5field-weighted citation impact, top 11% 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, 51 citations in OpenAlex.

  1. Hemodynamic Metrics and Arterial Dysfunction: Insights From a Novel Microfluidic Device.International journal for numerical methods in biomedical engineering · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Transcytosis of LDL Across Arterial Endothelium: Mechanisms and Therapeutic Targets.Arteriosclerosis, thrombosis, and vascular biology · 2025
    Review
  6. Article
  7. Molecular Mechanisms Regulating Vascular Endothelial Permeability.International journal of molecular sciences · 2024
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Leveraging avidin-biotin interaction to quantify permeability property of microvessels-on-a-chip networks.American journal of physiology. Heart and circulatory physiology · 2022
    Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Mean GhimDepartment of Bioengineering, Imperial College London, London, United Kingdom.
Paola AlpresaDepartment of Bioengineering, Imperial College London, London, United Kingdom.
Sung-Wook YangDepartment of Bioengineering, Imperial College London, London, United Kingdom.
Sietse T BraakmanDepartment of Bioengineering, Imperial College London, London, United Kingdom.
Stephen G GrayDepartment of Bioengineering, Imperial College London, London, United Kingdom.
Spencer J SherwinDepartment of Aeronautics, Imperial College London, London, United Kingdom; and.
Maarten van ReeuwijkDepartment of Civil and Environmental Engineering, Imperial College London, London, United Kingdom.
Peter D WeinbergDepartment of Bioengineering, Imperial College London, London, United Kingdom; p.weinberg@imperial.ac.uk.
Imperial College London · GB

Funding

British Heart Foundation PG/15/102/31890
6 · The paper itself

Abstract

Transport of macromolecules across vascular endothelium and its modification by fluid mechanical forces are important for normal tissue function and in the development of atherosclerosis. However, the routes by which macromolecules cross endothelium, the hemodynamic stresses that maintain endothelial physiology or trigger disease, and the dependence of transendothelial transport on hemodynamic stresses are controversial. We visualized pathways for macromolecule transport and determined the effect on these pathways of different types of flow. Endothelial monolayers were cultured under static conditions or on an orbital shaker producing different flow profiles in different parts of the wells. Fluorescent tracers that bound to the substrate after crossing the endothelium were used to identify transport pathways. Maps of tracer distribution were compared with numerical simulations of flow to determine effects of different shear stress metrics on permeability. Albumin-sized tracers dominantly crossed the cultured endothelium via junctions between neighboring cells, high-density lipoprotein-sized tracers crossed at tricellular junctions, and low-density lipoprotein-sized tracers crossed through cells. Cells aligned close to the angle that minimized shear stresses across their long axis. The rate of paracellular transport under flow correlated with the magnitude of these minimized transverse stresses, whereas transport across cells was uniformly reduced by all types of flow. These results contradict the long-standing two-pore theory of solute transport across microvessel walls and the consensus view that endothelial cells align with the mean shear vector. They suggest that endothelial cells minimize transverse shear, supporting its postulated proatherogenic role. Preliminary data show that similar tracer techniques are practicable in vivo.

Indexed as

AlgorithmsAnimalsAortaBiological Transport, ActiveCell NucleusCells, CulturedEndothelial CellsEndothelium, VascularIntercellular JunctionsLipoproteins, LDLMacromolecular SubstancesStress, MechanicalSwineLipoproteins, LDLMacromolecular Substancesendothelial permeabilitytransverse wall shear stresstricellular junctionvesicleswall shear stress

Identifiers

PMID28754719
PMCPMC5792200
OpenAlexW2740724466

What OpenQuestion holds

Textmetadata
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.