Evidence map›Paper›PMID 11385507›Full record

ArticleNature medicine2001

Lack of macrophage fatty-acid-binding protein aP2 protects mice deficient in apolipoprotein E against atherosclerosis.

Liza Makowski, Jeffrey B Boord, Kazuhisa Maeda, Vladimir R Babaev, K Teoman Uysal, Maureen A Morgan, Rex A Parker, Jill Suttles, Sergio Fazio, Gökhan S Hotamisligil and 1 more

Erratum issuedAbstract read
In one paragraph

Article in Nature medicine, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 316 papers.

0numbers the graph read from it
0cells of the map it votes in
316citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

316 citing papers in PubMed, 689 citations in OpenAlex.

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  12. Adipokines: masterminds of metabolic inflammation.Nature reviews. Immunology · 2025
    Review
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256 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

Liza Makowski *Division of Biological Sciences and Department of Nutrition, Harvard School of Public Health, Boston, Massachusetts, USA.
Jeffrey B Boord *Departments of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Kazuhisa MaedaDivision of Biological Sciences and Department of Nutrition, Harvard School of Public Health, Boston, Massachusetts, USA.
Vladimir R BabaevDepartments of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
K Teoman UysalDivision of Biological Sciences and Department of Nutrition, Harvard School of Public Health, Boston, Massachusetts, USA.
Maureen A MorganBristol-Myers Squibb PRI, Department of Metabolic Research, Princeton, New Jersey, USA.
Rex A ParkerBristol-Myers Squibb PRI, Department of Metabolic Research, Princeton, New Jersey, USA.
Jill SuttlesDepartment of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, Kentucky, USA.
Sergio FazioDepartments of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Gökhan S HotamisligilDivision of Biological Sciences and Department of Nutrition, Harvard School of Public Health, Boston, Massachusetts, USA.
MacRae F LintonDepartments of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Harvard University · USVanderbilt University Medical Center · USBristol-Myers Squibb (United States) · USUniversity of Louisville · US

Funding

Translational Research in Endocrinology And Diabetes (TREAD)T32DK007061 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Sarah S Jaser, KEVIN D NISWENDER · 1986 to 2026
$8.0M
ROLE OF FATTY ACID BINDING PROTEINS IN ATHEROSCLEROSISR01HL065405 · NHLBI · VANDERBILT UNIVERSITY · PI LINTON, MACRAE F · 2000 to 2009
$4.0M
Role of Fatty Acid Binding Proteins in Lipid SignalingF32HL075970 · NHLBI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI HAYES, LIZA MAKOWSKI · 2004 to 2005
$91k
NHLBI NIH HHS F32 HL075970NHLBI NIH HHS HL65405-01NHLBI NIH HHS R01 HL065405NIDDK NIH HHS T32 DK007061NIDDK NIH HHS T32 DK7061
6 · The paper itself

Abstract

The adipocyte fatty-acid-binding protein, aP2, has an important role in regulating systemic insulin resistance and lipid metabolism. Here we demonstrate that aP2 is also expressed in macrophages, has a significant role in their biological responses and contributes to the development of atherosclerosis. Apolipoprotein E (ApoE)-deficient mice also deficient for aP2 showed protection from atherosclerosis in the absence of significant differences in serum lipids or insulin sensitivity. aP2-deficient macrophages showed alterations in inflammatory cytokine production and a reduced ability to accumulate cholesterol esters when exposed to modified lipoproteins. Apoe-/- mice with Ap2+/+ adipocytes and Ap2-/- macrophages generated by bone-marrow transplantation showed a comparable reduction in atherosclerotic lesions to those with total aP2 deficiency, indicating an independent role for macrophage aP2 in atherogenesis. Through its distinct actions in adipocytes and macrophages, aP2 provides a link between features of the metabolic syndrome and could be a new therapeutic target for the prevention of atherosclerosis.

Indexed as

Neoplasm ProteinsNerve Tissue ProteinsTumor Suppressor ProteinsAdipocytesAnimalsAortaApolipoproteins EArteriosclerosisBone Marrow TransplantationCarrier ProteinsCell LineCholesterol EstersDietFatty Acid-Binding Protein 7Fatty Acid-Binding ProteinsFemaleApolipoproteins ECarrier ProteinsCholesterol EstersFabp5 protein, mouseFABP7 protein, humanFabp7 protein, mouseFatty Acid-Binding Protein 7Fatty Acid-Binding ProteinsGlucoseInsulinInterleukin-1Interleukin-6LipidsNeoplasm ProteinsNerve Tissue ProteinsTumor Necrosis Factor-alphaTumor Suppressor Proteins

Identifiers

PMID11385507
PMCPMC4027052
OpenAlexW1577139444

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.