Evidence map›Paper›PMID 24833800›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2014

Myeloid cell-specific ATP-binding cassette transporter A1 deletion has minimal impact on atherogenesis in atherogenic diet-fed low-density lipoprotein receptor knockout mice.

Xin Bi, Xuewei Zhu, Chuan Gao, Swapnil Shewale, Qiang Cao, Mingxia Liu, Elena Boudyguina, Abraham K Gebre, Martha D Wilson, Amanda L Brown and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

26 citing papers in PubMed, 32 citations in OpenAlex.

  1. ILRUN Promotes Atherosclerosis Through Lipid-Dependent and Lipid-Independent Factors.Arteriosclerosis, thrombosis, and vascular biology · 2022
    Article
  2. Article
  3. Article
  4. Article
  5. Uncurtaining the pivotal role of ABC transporters in diabetes mellitus.Environmental science and pollution research international · 2021
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Beyond the Foam Cell: The Role of LXRs in Preventing Atherogenesis.International journal of molecular sciences · 2018
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Do the Apoe-/- and Ldlr-/- Mice Yield the Same Insight on Atherogenesis?Arteriosclerosis, thrombosis, and vascular biology · 2016
    Review
  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

11 authors at 1 institution in 1 country.

Xin BiFrom the Department of Pathology/Section on Lipid Sciences (X.B., X.Z., C.G., S.S., Q.C., M.L., E.B., A.K.G., M.D.W., A.L.B., J.S.P.) and Department of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC (J.S.P.).
Xuewei ZhuFrom the Department of Pathology/Section on Lipid Sciences (X.B., X.Z., C.G., S.S., Q.C., M.L., E.B., A.K.G., M.D.W., A.L.B., J.S.P.) and Department of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC (J.S.P.).
Chuan GaoFrom the Department of Pathology/Section on Lipid Sciences (X.B., X.Z., C.G., S.S., Q.C., M.L., E.B., A.K.G., M.D.W., A.L.B., J.S.P.) and Department of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC (J.S.P.).
Swapnil ShewaleFrom the Department of Pathology/Section on Lipid Sciences (X.B., X.Z., C.G., S.S., Q.C., M.L., E.B., A.K.G., M.D.W., A.L.B., J.S.P.) and Department of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC (J.S.P.).
Qiang CaoFrom the Department of Pathology/Section on Lipid Sciences (X.B., X.Z., C.G., S.S., Q.C., M.L., E.B., A.K.G., M.D.W., A.L.B., J.S.P.) and Department of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC (J.S.P.).
Mingxia LiuFrom the Department of Pathology/Section on Lipid Sciences (X.B., X.Z., C.G., S.S., Q.C., M.L., E.B., A.K.G., M.D.W., A.L.B., J.S.P.) and Department of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC (J.S.P.).
Elena BoudyguinaFrom the Department of Pathology/Section on Lipid Sciences (X.B., X.Z., C.G., S.S., Q.C., M.L., E.B., A.K.G., M.D.W., A.L.B., J.S.P.) and Department of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC (J.S.P.).
Abraham K GebreFrom the Department of Pathology/Section on Lipid Sciences (X.B., X.Z., C.G., S.S., Q.C., M.L., E.B., A.K.G., M.D.W., A.L.B., J.S.P.) and Department of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC (J.S.P.).
Martha D WilsonFrom the Department of Pathology/Section on Lipid Sciences (X.B., X.Z., C.G., S.S., Q.C., M.L., E.B., A.K.G., M.D.W., A.L.B., J.S.P.) and Department of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC (J.S.P.).
Amanda L BrownFrom the Department of Pathology/Section on Lipid Sciences (X.B., X.Z., C.G., S.S., Q.C., M.L., E.B., A.K.G., M.D.W., A.L.B., J.S.P.) and Department of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC (J.S.P.).
John S ParksFrom the Department of Pathology/Section on Lipid Sciences (X.B., X.Z., C.G., S.S., Q.C., M.L., E.B., A.K.G., M.D.W., A.L.B., J.S.P.) and Department of Biochemistry, Wake Forest School of Medicine, Winston-Salem, NC (J.S.P.). jparks@wakehealth.edu.
Wake Forest University · US

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
TISSUE CULTURE COREP01HL049373 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SHELNESS, GREGORY S · 1993 to 2012
$23.8M
The Wake Forest Center for Botanical Lipids and Inflammatory Disease PreventionP50AT002782 · NCCIH · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI CHILTON, FLOYD H · 2005 to 2014
$15.3M
The Role of Hepatocyte ABCA1 in Lipid Mobilization and TransportR01HL119962 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PARKS, JOHN S · 2013 to 2022
$3.9M
Macrophage, ABCA1, Inflammation, and AtherosclerosisR01HL094525 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI PARKS, JOHN S · 2009 to 2012
$1.5M
NCCIH NIH HHS AT002782NCCIH NIH HHS P50 AT002782NCI NIH HHS P30 CA012197NHLBI NIH HHS HL119962NHLBI NIH HHS HL49373NHLBI NIH HHS HL94525NHLBI NIH HHS P01 HL049373NHLBI NIH HHS R01 HL094525NHLBI NIH HHS R01 HL119962
6 · The paper itself

Abstract

objectiveTransplantation studies suggest that bone marrow cell ATP-binding cassette transporter A1 protects against atherosclerosis development. However, the in vivo effect of macrophage ATP-binding cassette transporter A1 expression on atherogenesis is not fully understood because bone marrow contains other leukocytes and hematopoietic stem and progenitor cells. Myeloid-specific ATP-binding cassette transporter A1 knockout mice in the low-density lipoprotein (LDL) receptor knockout C57BL/6 background were developed to address this question. APPROACH AND

resultsChow-fed myeloid-specific ATP-binding cassette transporter A1 knockout/LDL receptor knockout (double knockout [DKO]) versus LDL receptor knockout (single knockout [SKO]) mice had similar plasma lipid concentrations, but atherogenic diet (AD)-fed DKO mice had reduced plasma very-LDL (VLDL)/LDL concentrations resulting from decreased hepatic VLDL triglyceride secretion. Resident peritoneal macrophages from AD-fed DKO versus SKO mice had significantly higher cholesterol content but similar proinflammatory gene expression. Atherosclerosis extent was similar between genotypes after 10 to 16 weeks of AD but increased modestly in DKO mice by 24 weeks of AD. Lesional macrophage content was similar, likely because of the higher monocyte flux through aortic root lesions in DKO versus SKO mice. After transplantation of DKO or SKO bone marrow into SKO mice and 16 weeks of AD feeding, atherosclerosis extent was similar and plasma apolipoprotein B lipoproteins were reduced in mice receiving DKO bone marrow. When differences in plasma VLDL/LDL concentrations were minimized by maintaining mice on chow for 24 weeks, DKO mice had modest, but significantly more, atherosclerosis compared with SKO mice.

conclusionsMyeloid cell ATP-binding cassette transporter A1 increases hepatic VLDL triglyceride secretion and plasma VLDL/LDL concentrations in AD-fed LDL receptor knockout mice, offsetting its atheroprotective role in decreasing macrophage cholesterol content, resulting in a minimal increase in atherosclerosis.

Indexed as

AnimalsAortaAtherosclerosisATP Binding Cassette Transporter 1Bone Marrow TransplantationCholesterolCholesterol, LDLCholesterol, VLDLDiet, AtherogenicFemaleGenotypeMacrophages, PeritonealMaleMiceMice, Inbred C57BLMice, KnockoutAbca1 protein, mouseATP Binding Cassette Transporter 1CholesterolCholesterol, LDLCholesterol, VLDLReceptors, LDLTriglyceridesatherosclerosiscardiovascular diseasescholesterollipidslipoproteins

Identifiers

PMID24833800
PMCPMC4140956
OpenAlexW2168420993

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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.