Evidence map›Paper›PMID 16565511›Full record

ArticleThe American journal of pathology2006

Up-regulated expression of the CXCR2 ligand KC/GRO-alpha in atherosclerotic lesions plays a central role in macrophage accumulation and lesion progression.

William A Boisvert, David M Rose, Kristen A Johnson, Maria E Fuentes, Sergio A Lira, Linda K Curtiss, Robert A Terkeltaub

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing 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

91 citing papers in PubMed, 185 citations in OpenAlex.

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31 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

7 authors at 5 institutions in 1 country.

William A BoisvertDepartment of Immunology,* The Scripps Research Institute, La Jolla, California, USA. wboisvert@rics.bwh.harvard.edu
David M Rose
Kristen A Johnson
Maria E Fuentes
Sergio A Lira
Linda K Curtiss
Robert A Terkeltaub
Scripps Research Institute · USUniversity of California San Diego Medical Center · USIcahn School of Medicine at Mount Sinai · USLa Roche College · USPalo Alto Institute · US

Funding

IMMUNOBIOLOGY OF APOLIPOPROTEIN ER01HL035297 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI CURTISS, LINDA K · 1986 to 2006
$2.4M
NPP1 and Molecular Mechanisms in Artery CalcificationR01HL077360 · NHLBI · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI TERKELTAUB, ROBERT A. · 2004 to 2012
$2.2M
THE CHEMOKINE RECEPTOR CXCR-2 IN ATHEROSCLEROSISR01HL061731 · NHLBI · SCRIPPS RESEARCH INSTITUTE · PI BOISVERT, WILLIAM A · 1999 to 2002
$1.1M
LOCALLY PRODUCED APOLIPOPROTEIN E IN ATHEROSCLEROSISR29HL057934 · NHLBI · SCRIPPS RESEARCH INSTITUTE · PI BOISVERT, WILLIAM A · 1997 to 2000
$127k
NHLBI NIH HHS HL-35297NHLBI NIH HHS HL-57934NHLBI NIH HHS HL-61731NHLBI NIH HHS HL-77360NHLBI NIH HHS R01 HL035297NHLBI NIH HHS R01 HL077360
6 · The paper itself

Abstract

Macrophage-mediated inflammation is central to atherogenesis. We have determined previously that the CXC chemokine receptor CXCR2 is involved in advanced atherosclerosis. We sought to determine whether one of the ligands of CXCR2, KC/GRO-alpha, can also modulate atherogenesis. KC/GRO-alpha(-/-) mice were generated and mated with the atherosclerosis-prone LDLR(-/-) mice. There was a significant reduction in atherosclerosis in mice lacking KC/GRO-alpha; however, this reduction was only approximately half that seen previously in mice lacking CXCR2 in the leukocyte. To determine whether CXCR2 is involved in the early formation of atherosclerosis, leukocyte-specific CXCR2(-/-) chimeric mice on LDLR(-/-) background were generated. Early fatty streak lesion formation in these mice was not affected by leukocyte CXCR2 deficiency whereas lesions were less developed in mice lacking leukocyte CXCR2 when atherosclerosis was allowed to progress to the intermediate stage. Macrophages were relatively sparse in the lesions of leukocyte CXCR2(-/-) mice despite robust MCP-1 expression. These studies indicate that KC/GRO-alpha/CXCR2 does not play a critical role in recruitment of macrophages into early atherosclerotic lesions but both arterial KC/GRO-alpha and leukocyte-specific CXCR2 expression are central to macrophage accumulation in established fatty streak lesions.

Indexed as

Up-RegulationAnimalsAortaAtherosclerosisChemokine CCL2Chemokine CXCL1Chemokines, CXCChimeraIntercellular Signaling Peptides and ProteinsLeukocytesMacrophagesMaleMiceMice, KnockoutReceptors, Interleukin-8BCcl2 protein, mouseChemokine CCL2Chemokine CXCL1Chemokines, CXCCxcl1 protein, mouseIntercellular Signaling Peptides and ProteinsReceptors, Interleukin-8B

Identifiers

PMID16565511
PMCPMC1606562
OpenAlexW2083183631

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.