Evidence map›Paper›PMID 33190063›Full record

ArticlePlacenta2021

Pericytes on placental capillaries in terminal villi preferentially cover endothelial junctions in regions furthest away from the trophoblast.

Shelley E Harris, Kate Sh Matthews, Eleni Palaiologou, Stanimir A Tashev, Emma M Lofthouse, Jennifer Pearson-Farr, Patricia Goggin, David S Chatelet, David A Johnston, Maaike Sa Jongen and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Placenta, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Feto-placental blood vessel development.Development (Cambridge, England) · 2025
    Review
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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

13 authors at 1 institution in 1 country.

Shelley E HarrisHuman Development and Health, Faculty of Medicine, University of Southampton, UK.
Kate Sh MatthewsHuman Development and Health, Faculty of Medicine, University of Southampton, UK.
Eleni PalaiologouHuman Development and Health, Faculty of Medicine, University of Southampton, UK.
Stanimir A TashevBiomedical Imaging Unit, Faculty of Medicine, University of Southampton, UK.
Emma M LofthouseHuman Development and Health, Faculty of Medicine, University of Southampton, UK.
Jennifer Pearson-FarrHuman Development and Health, Faculty of Medicine, University of Southampton, UK.
Patricia GogginBiomedical Imaging Unit, Faculty of Medicine, University of Southampton, UK.
David S ChateletBiomedical Imaging Unit, Faculty of Medicine, University of Southampton, UK.
David A JohnstonBiomedical Imaging Unit, Faculty of Medicine, University of Southampton, UK.
Maaike Sa JongenHuman Development and Health, Faculty of Medicine, University of Southampton, UK.
Anton M PageBiomedical Imaging Unit, Faculty of Medicine, University of Southampton, UK.
Jane K ClealHuman Development and Health, Faculty of Medicine, University of Southampton, UK; Institute for Life Sciences, University of Southampton, UK.
Rohan M LewisHuman Development and Health, Faculty of Medicine, University of Southampton, UK; Institute for Life Sciences, University of Southampton, UK. Electronic address: rohan.lewis@soton.ac.uk.
University of Southampton · GB

Funding

Medical Research Council MR/L012626/1
6 · The paper itself

Abstract

introductionPericytes are a common feature in the placental microvasculature but their roles are not well understood. Pericytes may provide physical or endocrine support for endothelium and in some tissues mediate vasoconstriction.

methodsThis study uses serial block-face scanning electron microscopy (SBFSEM) to generate three-dimensional (3D) reconstructions of placental pericytes of the terminal villi and transmission electron microscopy (TEM) to study pericyte endothelial cell interactions. The proportion of endothelial cell junctions covered by pericytes was determined.

resultsThe detailed 3D models of placental pericytes show pericyte structure at a new level of detail. Placental pericytes have many fingers extending from the cell body which can span multiple capillary branches. The proportion of endothelial cell-cell junctions covered by pericytes was significantly higher than pericyte coverage of capillary endothelium as a whole (endothelium: 14%, junctions: 43%, p < 0.0001). However, the proportion of endothelial cell-cell junctions covered by pericytes in regions adjacent to trophoblast was reduced compared to regions >3 μm away from trophoblast (27% vs 62% respectively, p < 0.001). No junctional complexes were observed connecting pericytes and endothelial cells but there were regions of cell membrane with features suggestive of intercellular adhesions. DISCUSSION: These data suggest that the localisation of pericytes on the villous capillary is not random but organised in relation to both endothelial junctions and the location of adjacent trophoblast. This further suggests that pericyte coverage may favour capillary permeability in regions that are most important for exchange, but limit capillary permeability in other regions.

Indexed as

ActinsCapillariesChorionic VilliEndothelial CellsEndothelium, VascularFemaleHumansMicroscopy, Electron, ScanningPericytesPlacentaPregnancyTrophoblastsActinsMicrovasculaturePericytesPlacentaThree-dimensional imaging

Identifiers

PMID33190063
PMCPMC7921774
OpenAlexW3096585578

What OpenQuestion holds

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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.