Evidence map›Paper›PMID 19617532›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

Capillary morphogenesis protein-2 is the major receptor mediating lethality of anthrax toxin in vivo.

Shihui Liu, Devorah Crown, Sharmina Miller-Randolph, Mahtab Moayeri, Hailun Wang, Haijing Hu, Thomas Morley, Stephen H Leppla

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 112 papers.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

112 citing papers in PubMed, 158 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. ERK and c-Myc signaling in host-derived tumor endothelial cells is essential for solid tumor growth.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. American journal of physiology. Heart and circulatory physiology · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Tumor Imaging Using Radiolabeled Matrix Metalloproteinase-Activated Anthrax Proteins.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2019
    Article

52 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

8 authors at 2 institutions in 1 country.

Shihui LiuBacterial Toxins and Therapeutics Section, Laboratory of Bacterial Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA. shliu@niaid.nih.gov
Devorah Crown
Sharmina Miller-Randolph
Mahtab Moayeri
Hailun Wang
Haijing Hu
Thomas Morley
Stephen H Leppla
National Institute of Allergy and Infectious Diseases · USNational Institutes of Health · US

Funding

Structure and Function of Virulence Factors of Bacillus anthracisZIAAI001031 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI LEPPLA, STEPHEN · 2009 to 2018
$6.2M
Structure and Function of Virulence Factors of Bacillus anthracis Z01AI001031 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI LEPPLA, STEPHEN · 2008 to 2008
$899k
Intramural NIH HHS
6 · The paper itself

Abstract

Anthrax toxin, a major virulence factor of Bacillus anthracis, gains entry into target cells by binding to either of 2 von Willebrand factor A domain-containing proteins, tumor endothelium marker-8 (TEM8) and capillary morphogenesis protein-2 (CMG2). The wide tissue expression of TEM8 and CMG2 suggest that both receptors could play a role in anthrax pathogenesis. To explore the roles of TEM8 and CMG2 in normal physiology, as well as in anthrax pathogenesis, we generated TEM8- and CMG2-null mice and TEM8/CMG2 double-null mice by deleting TEM8 and CMG2 transmembrane domains. TEM8 and CMG2 were found to be dispensable for mouse development and life, but both are essential in female reproduction in mice. We found that the lethality of anthrax toxin for mice is mostly mediated by CMG2 and that TEM8 plays only a minor role. This is likely because anthrax toxin has approximately 11-fold higher affinity for CMG2 than for TEM8. Finally, the CMG2-null mice are also shown to be highly resistant to B. anthracis spore infection, attesting to the importance of both anthrax toxin and CMG2 in anthrax infections.

Indexed as

AnimalsAnthraxAntigens, BacterialBacillus anthracisBacterial ToxinsBinding SitesBiomarkers, TumorBlotting, WesternCells, CulturedFemaleFibroblastsGene ExpressionGenes, EssentialHost-Pathogen InteractionsMaleMembrane Proteinsanthrax toxinAntigens, BacterialAntxr1 protein, mouseAntxr2 protein, mouseBacterial ToxinsBiomarkers, TumorMembrane ProteinsMicrofilament ProteinsReceptors, Cell SurfaceReceptors, Peptide

Identifiers

PMID19617532
PMCPMC2718377
OpenAlexW2128855764

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.