Evidence map›Paper›PMID 15102799›Full record

ArticleInfection and immunity2004

Mycobacteria inhibit nitric oxide synthase recruitment to phagosomes during macrophage infection.

Barbara H Miller, Rutilio A Fratti, Jens F Poschet, Graham S Timmins, Sharon S Master, Marcos Burgos, Michael A Marletta, Vojo Deretic

Abstract read
In one paragraph

Article in Infection and immunity, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

54 citing papers in PubMed, 155 citations in OpenAlex.

  1. eLife · 2024
    Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Spatial Resolution ofFrontiers in immunology · 2022
    Article
  9. Microorganisms · 2021
    Review
  10. Article
  11. Review
  12. Review
  13. TheThe Yale journal of biology and medicine · 2019
    Review
  14. Article
  15. Article
  16. Continual renewal and replication of persistent Leishmania major parasites in concomitantly immune hosts.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  17. Review
  18. Review
  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

8 authors at 2 institutions in 1 country.

Barbara H MillerDepartment of Microbiology and Immunology, University of Michigan School of Medicine, Ann Arbor, Michigan 48109-0620, USA.
Rutilio A Fratti
Jens F Poschet
Graham S Timmins
Sharon S Master
Marcos Burgos
Michael A Marletta
Vojo Deretic
University of Michigan–Ann Arbor · USUniversity of New Mexico · US

Funding

Reaction and Diffusion of NO in Biological SystemsP01CA026731 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI WISHNOK, JOHN S. · 1985 to 2018
$25.4M
Pattern Recognition Receptors and Autophagy in Mtb Control in AIDSR01AI042999 · NIAID · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI DERETIC, VOJO P · 1998 to 2017
$6.6M
Pattern Recognition Receptors and Autophagy in Mtb Control in AIDSR37AI042999 · NIAID · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI VOJO P DERETIC · 2018 to 2026
$4.7M
NCI NIH HHS CA26731NCI NIH HHS P01 CA026731NIAID NIH HHS AI42999NIAID NIH HHS R01 AI042999
6 · The paper itself

Abstract

Inducible nitric oxide synthase (iNOS) is a cytoplasmic protein responsible for the generation of nitric oxide (NO. ) in macrophages. In this work, we hypothesized that the intracellular localization of iNOS is significant for effective delivery of NO. to phagosomes containing ingested microorganisms. Using immunofluorescence microscopy and Western blot analysis, iNOS was shown to localize in the vicinity of phagosomes containing latex beads in stimulated macrophages. iNOS also localized to phagosomes containing Escherichia coli. The colocalization of iNOS with ingested latex beads was an actin-dependent process, since treatment with the actin microfilament disrupter cytochalasin D prevented iNOS recruitment to latex bead phagosomes. In contrast to E. coli and inert particle phagosomes, mycobacterial phagosomes did not colocalize with iNOS. This study demonstrates that (i). iNOS can be recruited to phagosomes; (ii). this recruitment is dependent on a functional actin cytoskeleton; (iii). certain microorganisms have the ability to prevent or reduce colocalization with iNOS; and (iv). spatial exclusion of iNOS may play a role in Mycobacterium tuberculosis pathogenesis.

Indexed as

ActinsAnimalsCell LineCytoskeletonIn Vitro TechniquesMacrophage ActivationMacrophagesMiceMice, Inbred C57BLMice, KnockoutMycobacterium bovisMycobacterium tuberculosisNitric Oxide SynthaseNitric Oxide Synthase Type IIPhagosomesActinsNitric Oxide SynthaseNitric Oxide Synthase Type IINos2 protein, mouse

Identifiers

PMID15102799
PMCPMC387846
OpenAlexW2153819765

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.