Evidence map›Paper›PMID 10934232›Full record

ArticleThe Journal of experimental medicine2000

BLTR mediates leukotriene B(4)-induced chemotaxis and adhesion and plays a dominant role in eosinophil accumulation in a murine model of peritonitis.

A M Tager, J H Dufour, K Goodarzi, S D Bercury, U H von Andrian, A D Luster

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
6.7field-weighted citation impact, top 2% 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

63 citing papers in PubMed, 195 citations in OpenAlex.

  1. Review
  2. Article
  3. CCR3-dependent eosinophil recruitment is regulated by sialyltransferase ST3Gal-IV.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Review
  5. Activation of leukotriene BCellular & molecular immunology · 2024
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Leukotriene receptors as potential therapeutic targets.The Journal of clinical investigation · 2018
    Review
  15. The role of the LTBSeminars in immunology · 2017
    Review
  16. The yin and yang of leukotriene BSeminars in immunology · 2017
    Review
  17. Review
  18. Article
  19. Article
  20. Article

3 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

A M TagerCenter for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, USA.
J H Dufour
K Goodarzi
S D Bercury
U H von Andrian
A D Luster
Harvard University · US

Funding

Lung-Resident Memory Th2 cells in Asthma - New Therapeutic TargetsR01AI040618 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI LUSTER, ANDREW D · 1997 to 2022
$5.6M
IP 10--ITS ROLE IN INFLAMMATION AND CANCER THERAPYR01CA069212 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI LUSTER, ANDREW D · 1996 to 2014
$5.6M
RECEPTOR TOPOGRAPHY IN MICROVASCULAR LEUKOCYTE ADHESIONR01HL054936 · NHLBI · IMMUNE DISEASE INSTITUTE, INC. · PI VON ANDRIAN, ULRICH H · 1996 to 2005
$2.2M
T CELL AND EOSINOPHIL RECRUITMENT IN LUNG FIBROSISK08HL004087 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI TAGER, ANDREW M · 1999 to 2003
$519k
CXCR3 MEDIATED SIGNAL TRANSDUCTIONF32CA088721 · NCI · YALE UNIVERSITY · PI DUFOUR, JENNIFER HODGE · 2000 to 2002
$119k
NCI NIH HHS F32 CA088721NCI NIH HHS F32-CA88721NCI NIH HHS R01 CA069212NHLBI NIH HHS KO8-HL04087NHLBI NIH HHS R01 HL054936NHLBI NIH HHS R01-HL54936NIAID NIH HHS R01 AI040618
6 · The paper itself

Abstract

Leukotriene B(4) (LTB(4)) is a potent chemoattractant active on multiple leukocytes, including neutrophils, macrophages, and eosinophils, and is implicated in the pathogenesis of a variety of inflammatory processes. A seven transmembrane-spanning, G protein-coupled receptor, called BLTR (LTB(4) receptor), has recently been identified as an LTB(4) receptor. To determine if BLTR is the sole receptor mediating LTB(4)-induced leukocyte activation and to determine the role of LTB(4) and BLTR in regulating leukocyte function in inflammation in vivo, we generated a BLTR-deficient mouse by targeted gene disruption. This mouse reveals that BLTR alone is responsible for LTB(4)-mediated leukocyte calcium flux, chemotaxis, and firm adhesion to endothelium in vivo. Furthermore, despite the apparent functional redundancy with other chemoattractant-receptor pairs in vitro, LTB(4) and BLTR play an important role in the recruitment and/or retention of leukocytes, particularly eosinophils, to the inflamed peritoneum in vivo. These studies demonstrate that BLTR is the key receptor that mediates LTB(4)-induced leukocyte activation and establishes a model to decipher the functional roles of BLTR and LTB(4) in vivo.

Indexed as

Chemotaxis, LeukocyteAnimalsCalciumCell AdhesionChemotactic FactorsDisease Models, AnimalEosinophilsGene TargetingLeukotriene B4Macrophages, PeritonealMiceMice, Inbred C57BLMice, KnockoutMusclesNeutrophilsPeritonitisCalciumChemotactic FactorsLeukotriene B4Receptors, Leukotriene B4Thioglycolates

Identifiers

PMID10934232
PMCPMC2193216
OpenAlexW2170049370

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.