Evidence map›Paper›PMID 20644116›Full record

ArticleBlood2010

Shiga toxin B subunits induce VWF secretion by human endothelial cells and thrombotic microangiopathy in ADAMTS13-deficient mice.

Jing Huang, David G Motto, David R Bundle, J Evan Sadler

Abstract read
In one paragraph

Article in Blood, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
5.0field-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

48 citing papers in PubMed, 68 citations in OpenAlex.

  1. Trial
  2. Mouse models to study von Willebrand factor in thrombosis: a scoping review.Research and practice in thrombosis and haemostasis · 2026
    Article
  3. Review
  4. Article
  5. Microfluidic Shear-Based Assay for Assessing ADAMTS13 Activity Under Flow.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. ABToxins · 2022
    Review
  12. Article
  13. Article
  14. Atypical hemolytic uremic syndrome: a case report.Journal of medical case reports · 2020
    Article
  15. Article
  16. Pathogenesis of Atypical Hemolytic Uremic Syndrome.Journal of atherosclerosis and thrombosis · 2019
    Review
  17. Article
  18. Article
  19. Article
  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

4 authors at 3 institutions in 2 countries.

Jing HuangDepartments of Medicine, Biochemistry, and Molecular Biophysics, Washington University School of Medicine, St Louis, MO 63110, USA.
David G Motto
David R Bundle
J Evan Sadler
Washington University in St. Louis · USUniversity of Alberta · CAUniversity of Iowa · US

Funding

VON WILLEBRAND FACTOR MULTIMER ASSEMBLY AND STRUCTURER01HL072917 · NHLBI · WASHINGTON UNIVERSITY · PI SADLER, J EVAN · 2003 to 2012
$4.4M
Regulation of ADAMTS13 ActivityR01HL089746 · NHLBI · WASHINGTON UNIVERSITY · PI SADLER, J EVAN · 2007 to 2011
$2.1M
Functional analysis of ADAMTS13 K08HL076539 · NHLBI · UNIVERSITY OF IOWA · PI MOTTO, DAVID G · 2006 to 2010
$632k
NHLBI NIH HHS HL076539NHLBI NIH HHS HL72917NHLBI NIH HHS HL89746NHLBI NIH HHS K08 HL076539NHLBI NIH HHS R01 HL072917NHLBI NIH HHS R01 HL089746
6 · The paper itself

Abstract

Diarrhea-associated hemolytic uremic syndrome (D+HUS) is the most common cause of acute renal failure among children. Renal damage in D+HUS is caused by Shiga toxin (Stx), which is elaborated by Shigella dysenteriae and certain strains of Escherichia coli, in North America principally E coli O157:H7. Recent studies demonstrate that Stx also induces von Willebrand factor (VWF) secretion by human endothelial cells and causes thrombotic thrombocytopenic purpura, a disease with similarities to D+HUS, in Adamts13(-/-) mice. Stx occurs in 2 variants, Stx1 and Stx2, each of which is composed of 1 catalytically active A subunit that is responsible for cytotoxicity, and 5 identical B subunits that mediate binding to cell-surface globo-triaosylceramide. We now report that B subunits from Stx1 or Stx2 can stimulate the acute secretion of VWF in the absence of the cytotoxic A subunit. This rapid effect requires binding and clustering of globotriaosylceramide, and depends on plasma membrane cholesterol and caveolin-1 but not clathrin. Furthermore, similar to Stx2 holotoxin, the isolated Stx2B subunits induce thrombotic microangiopathy in Adamts13(-/-) mice. These results demonstrate the existence of a novel Stx B-induced lipid raft-dependent signaling pathway in endothelial cells that may be responsible for some of the biological effects attributed previously to the cytotoxic Stx A subunit.

Indexed as

ADAMTS13 ProteinAnimalsCaveolin 1Cell LineCholera ToxinCholesterolClathrinEndothelial CellsGene DeletionGene Knockdown TechniquesHumansMetalloendopeptidasesMiceMice, Inbred C57BLShiga ToxinsShigella dysenteriaeADAMTS13 ProteinADAMTS13 protein, mouseCaveolin 1Cholera ToxinCholesterolClathringlobotriaosylceramideMetalloendopeptidasesShiga ToxinsstxB toxinTrihexosylceramidesvon Willebrand Factor

Identifiers

PMID20644116
PMCPMC2981485
OpenAlexW2005741975

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.