Evidence map›Paper›PMID 11602638›Full record

ArticleThe Journal of experimental medicine2001

Legionella pneumophila is internalized by a macropinocytotic uptake pathway controlled by the Dot/Icm system and the mouse Lgn1 locus.

M Watarai, I Derre, J Kirby, J D Growney, W F Dietrich, R R Isberg

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
–field-weighted citation impact
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

74 citing papers in PubMed.

  1. Life science alliance · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Membrane-dependent actin polymerization mediated by thebioRxiv : the preprint server for biology · 2023
    Article
  6. Platelets promote human macrophages-mediated macropinocytosis ofFrontiers in cellular and infection microbiology · 2023
    Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. The Role of Macrophages inFrontiers in immunology · 2020
    Review
  12. Frontiers in cellular and infection microbiology · 2020
    Article
  13. Phosphoinositides and the Fate ofFrontiers in immunology · 2020
    Review
  14. Journal of bacteriology · 2019
    Article
  15. Review
  16. Article
  17. Crucial Role ofFrontiers in microbiology · 2018
    Article
  18. Review
  19. Polar delivery ofProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  20. Article

14 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

6 authors.

M WataraiHoward Hughes Medical Institute, Tufts University School of Medicine, Boston, MA 02111, USA.
I Derre
J Kirby
J D Growney
W F Dietrich
R R Isberg

Funding

LEGIONELLA PNEUMOPHILA VIRULENCE FACTORS DEFINED IN VIVOK08AI001402 · NIAID · TUFTS UNIVERSITY BOSTON · PI KIRBY, JAMES E · 1996 to 2000
$121k
NIAID NIH HHS AI-01402
6 · The paper itself

Abstract

The products of the Legionella pneumophila dot/icm genes enable the bacterium to replicate within a macrophage vacuole. This study demonstrates that the Dot/Icm machinery promotes macropinocytotic uptake of L. pneumophila into mouse macrophages. In mouse strains harboring a permissive Lgn1 allele, L. pneumophila promoted formation of vacuoles that were morphologically similar to macropinosomes and dependent on the presence of an intact Dot/Icm system. Macropinosome formation appeared to occur during, rather than after, the closure of the plasma membrane about the bacterium, since a fluid-phase marker preloaded into the macrophage endocytic path failed to label the bacterium-laden macropinosome. The resulting macropinosomes were rich in GM1 gangliosides and glycosylphosphatidylinositol-linked proteins. The Lgn1 allele restrictive for L. pneumophila intracellular replication prevented dot/icm-dependent macropinocytosis, with the result that phagosomes bearing the microorganism were targeted into the endocytic network. Analysis of macrophages from recombinant inbred mouse strains support the model that macropinocytotic uptake is controlled by the Lgn1 locus. These results indicate that the products of the dot/icm genes and Lgn1 are involved in controlling an internalization route initiated at the time of bacterial contact with the plasma membrane.

Indexed as

AnimalsBone Marrow CellsCell MembraneCells, CulturedFemaleGenes, BacterialLegionella pneumophilaMacrophagesMiceMice, Inbred AMice, Inbred C57BLPinocytosis

Identifiers

PMID11602638
PMCPMC2193510

What OpenQuestion holds

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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.