Evidence map›Paper›PMID 16611231›Full record

ArticleCellular microbiology2006

Cholesterol-rich membrane microdomains mediate cell cycle arrest induced by Actinobacillus actinomycetemcomitans cytolethal-distending toxin.

Kathleen Boesze-Battaglia, Dave Besack, Terry McKay, Ali Zekavat, Linda Otis, Kelly Jordan-Sciutto, Bruce J Shenker

Open access · bronzeAbstract read
In one paragraph

Article in Cellular microbiology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

46 citing papers in PubMed, 80 citations in OpenAlex.

  1. TM9SF4 acts as a receptor mediatingFrontiers in cellular and infection microbiology · 2026
    Article
  2. Article
  3. Pathogens (Basel, Switzerland) · 2024
    Article
  4. Article
  5. Revisiting bacterial cytolethal distending toxin structure and function.Frontiers in cellular and infection microbiology · 2023
    Article
  6. Review
  7. International journal of molecular sciences · 2022
    Article
  8. Review
  9. The Active Subunit of the Cytolethal Distending Toxin, CdtB, Derived From BothFrontiers in cellular and infection microbiology · 2021
    Article
  10. Article
  11. Review
  12. Article
  13. Virulence and Pathogenicity Properties ofPathogens (Basel, Switzerland) · 2019
    Review
  14. Review
  15. Internalization of the Active Subunit of theFrontiers in cellular and infection microbiology · 2017
    Article
  16. Article
  17. Article
  18. Article
  19. A Journey of Cytolethal Distending Toxins through Cell Membranes.Frontiers in cellular and infection microbiology · 2016
    Review
  20. Review
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 1 institution in 1 country.

Kathleen Boesze-BattagliaDepartment of Biochemistry, University of Pennsylvania School of Dental Medicine, Philadelphia, PA, USA. battagli@biochem.dental.upenn.edu
Dave Besack
Terry McKay
Ali Zekavat
Linda Otis
Kelly Jordan-Sciutto
Bruce J Shenker
University of Pennsylvania · US

Funding

BACTERIA &LYMPHOCYTE SUPPRESSION IN PERIODONTITISR01DE006014 · NIDCR · UNIVERSITY OF PENNSYLVANIA · PI SHENKER, BRUCE J · 1985 to 2021
$8.6M
MEMBRANE FUSION IN RETINAL ROD OUTER SEGMENTSR01EY010420 · NEI · UNIV OF MED/DENT NJ-SCH OSTEOPATHIC MED · PI BOESZE-BATTAGLIA, KATHLEEN · 1999 to 2016
$4.7M
Nikon A1R confocal laser microscope system for live cell imagingS10RR026365 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI BOESZE-BATTAGLIA, KATHLEEN · 2010 to 2010
$500k
A Role for Melanoregulin in RPE-mediated PhagocytosisR21EY018705 · NEI · UNIVERSITY OF PENNSYLVANIA · PI BOESZE-BATTAGLIA, KATHLEEN · 2009 to 2010
$437k
MEMBRANE FUSION IN RETINAL ROD OUTER SEGMENTSR29EY010420 · NEI · UNIV OF MED/DENT NJ-SCH OSTEOPATHIC MED · PI BOESZE-BATTAGLIA, KATHLEEN B · 1994 to 1998
–
NCRR NIH HHS S10 RR026365NEI NIH HHS R01 EY010420NEI NIH HHS R21 EY018705NEI NIH HHS R29 EY010420NIDCR NIH HHS DE06014NIDCR NIH HHS R01 DE006014
6 · The paper itself

Abstract

We have previously shown that Actinobacillus actinomycetemcomitans cytolethal-distending toxin (Cdt) is a potent immunosuppressive agent that induces G2/M arrest in human lymphocytes. In this study, we explored the possibility that Cdt-mediated immunotoxicity involves lipid membrane microdomains. We first determined that following treatment of Jurkat cells with Cdt holotoxin all three Cdt subunits localize to these microdomains. Laser confocal microscopy was employed to colocalize the subunits with GM1-enriched membrane regions which are characteristic of membrane rafts. Western blot analysis of isolated lipid rafts also demonstrated the presence of Cdt peptides. Cholesterol depletion, using methyl beta-cyclodextrin, protected cells from the ability of the Cdt holotoxin to induce G2 arrest. Moreover, cholesterol depletion reduced the ability of the toxin to associate with Jurkat cells. Thus, lipid raft integrity is vital to the action of Cdt on host cells. The implications of our observations with respect to Cdt mode of action are discussed.

Indexed as

Cell CycleAggregatibacter actinomycetemcomitansAntigens, CDBacterial Toxinsbeta-CyclodextrinsCholesterolGangliosidosis, GM1HumansJurkat CellsMembrane MicrodomainsProtein SubunitsReceptors, TransferrinAntigens, CDBacterial Toxinsbeta-CyclodextrinsCD71 antigenCholesterolcytolethal distending toxin, Actinobacillus actinomycetemcomitansmethyl-beta-cyclodextrinProtein SubunitsReceptors, Transferrin

Identifiers

PMID16611231
PMCPMC4732718
OpenAlexW2027551392

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.