Evidence map›Paper›PMID 24348256›Full record

ArticlePLoS pathogens2013

Placental syncytium forms a biophysical barrier against pathogen invasion.

Varvara B Zeldovich, Casper H Clausen, Emily Bradford, Daniel A Fletcher, Emin Maltepe, Jennifer R Robbins, Anna I Bakardjiev

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

64 citing papers in PubMed, 112 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Hyperglycemia enhances group BFrontiers in immunology · 2025
    Article
  11. A Review of Emerging Viral Pathogens and Current Concerns for Vertical Transmission of Infection.Medical science monitor : international medical journal of experimental and clinical research · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Trophoblast Syncytialization: A Metabolic Crossroads.Results and problems in cell differentiation · 2024
    Article
  19. Review
  20. Review

4 more citing papers are in PubMed but not listed here.

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 1 country.

Varvara B ZeldovichDepartment of Pediatrics, University of California, San Francisco, San Francisco, California, United States of America ; Program in Microbial Pathogenesis and Host Defense, University of California, San Francisco, San Francisco, California, United States of America.
Casper H ClausenDepartment of Bioengineering and Program in Biophysics, University of California, Berkeley, Berkeley, California, United States of America.
Emily BradfordDepartment of Pediatrics, University of California, San Francisco, San Francisco, California, United States of America ; Program in Microbial Pathogenesis and Host Defense, University of California, San Francisco, San Francisco, California, United States of America ; Biomedical Sciences Program, University of California, San Francisco, San Francisco, California, United States of America.
Daniel A FletcherDepartment of Bioengineering and Program in Biophysics, University of California, Berkeley, Berkeley, California, United States of America.
Emin MaltepeDepartment of Pediatrics, University of California, San Francisco, San Francisco, California, United States of America ; Biomedical Sciences Program, University of California, San Francisco, San Francisco, California, United States of America.
Jennifer R RobbinsDepartment of Pediatrics, University of California, San Francisco, San Francisco, California, United States of America ; Program in Microbial Pathogenesis and Host Defense, University of California, San Francisco, San Francisco, California, United States of America ; Department of Biology, Xavier University, Cincinnati, Ohio, United States of America.
Anna I BakardjievDepartment of Pediatrics, University of California, San Francisco, San Francisco, California, United States of America ; Program in Microbial Pathogenesis and Host Defense, University of California, San Francisco, San Francisco, California, United States of America ; Biomedical Sciences Program, University of California, San Francisco, San Francisco, California, United States of America.
University of California, San Francisco · USUniversity of California, Berkeley · US

Funding

Integrating Environmental Cues at the Maternal-Fetal Vascular InterfaceR01HD072455 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MALTEPE, EMIN · 2012 to 2023
$4.3M
Role of Host Cells in Invasive ListeriosisR01AI084928 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BAKARDJIEV, ANNA · 2010 to 2016
$2.7M
Mechanical Regulation of Actin NetworksR01GM074751 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI FLETCHER, DANIEL A · 2008 to 2015
$2.4M
NIAID NIH HHS R01 AI084928NIAID NIH HHS R01AI84929NICHD NIH HHS R01 HD072455NIGMS NIH HHS R01 GM074751
6 · The paper itself

Abstract

Fetal syncytiotrophoblasts form a unique fused multinuclear surface that is bathed in maternal blood, and constitutes the main interface between fetus and mother. Syncytiotrophoblasts are exposed to pathogens circulating in maternal blood, and appear to have unique resistance mechanisms against microbial invasion. These are due in part to the lack of intercellular junctions and their receptors, the Achilles heel of polarized mononuclear epithelia. However, the syncytium is immune to receptor-independent invasion as well, suggesting additional general defense mechanisms against infection. The difficulty of maintaining and manipulating primary human syncytiotrophoblasts in culture makes it challenging to investigate the cellular and molecular basis of host defenses in this unique tissue. Here we present a novel system to study placental pathogenesis using murine trophoblast stem cells (mTSC) that can be differentiated into syncytiotrophoblasts and recapitulate human placental syncytium. Consistent with previous results in primary human organ cultures, murine syncytiotrophoblasts were found to be resistant to infection with Listeria monocytogenes via direct invasion and cell-to-cell spread. Atomic force microscopy of murine syncytiotrophoblasts demonstrated that these cells have a greater elastic modulus than mononuclear trophoblasts. Disruption of the unusually dense actin structure--a diffuse meshwork of microfilaments--with Cytochalasin D led to a decrease in its elastic modulus by 25%. This correlated with a small but significant increase in invasion of L. monocytogenes into murine and human syncytium. These results suggest that the syncytial actin cytoskeleton may form a general barrier against pathogen entry in humans and mice. Moreover, murine TSCs are a genetically tractable model system for the investigation of specific pathways in syncytial host defenses.

Indexed as

AnimalsBiophysical PhenomenaCells, CulturedFemaleGiant CellsHost-Pathogen InteractionsHumansImmunity, InnateInfectious Disease Transmission, VerticalListeria monocytogenesListeriosisMiceMice, Inbred C57BLPlacentaPregnancyPregnancy Complications, Infectious

Identifiers

PMID24348256
PMCPMC3861541
OpenAlexW2039921504

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.