Evidence map›Paper›PMID 28768900›Full record

ArticleJCI insight2017

Plasminogen promotes cholesterol efflux by the ABCA1 pathway.

Nathalie Pamir, Patrick M Hutchins, Graziella E Ronsein, Hao Wei, Chongren Tang, Riku Das, Tomas Vaisar, Edward Plow, Volker Schuster, Marlys L Koschinsky and 6 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
5.7field-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

33 citing papers in PubMed, 42 citations in OpenAlex.

  1. Trial
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  10. Clot or Not? Reviewing the Reciprocal Regulation Between Lipids and Blood Clotting.Arteriosclerosis, thrombosis, and vascular biology · 2024
    Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Correlations between the NMR Lipoprotein Profile,International journal of molecular sciences · 2023
    Article
  16. Article
  17. Article
  18. Article
  19. Molecular Patterns of Extreme and Persistent Cholesterol Efflux Capacity.Arteriosclerosis, thrombosis, and vascular biology · 2021
    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

16 authors at 6 institutions in 2 countries.

Nathalie PamirDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Patrick M HutchinsDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Graziella E RonseinDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Hao WeiDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Chongren TangDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Riku DasDepartment of Molecular Cardiology, Cleveland Clinic, Cleveland, Ohio, USA.
Tomas VaisarDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Edward PlowDepartment of Molecular Cardiology, Cleveland Clinic, Cleveland, Ohio, USA.
Volker SchusterHospital for Children and Adolescents, Medical Faculty of Leipzig University, Leipzig, Germany.
Marlys L KoschinskyRobarts Research Institute, Schulich School of Medicine and Dentistry, The University of Western Ontario, London, Ontario, Canada.
Catherine A ReardonBen May Research Institute, University of Chicago, Illinois, USA.
Richard WeinbergDepartment of Internal Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
David A DichekDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Santica MarcovinaDepartment of Medicine, University of Washington, Seattle, Washington, USA.
Godfrey S GetzDepartment of Pathology, University of Chicago, Chicago, Illinois, USA.
Jay W HeineckeDepartment of Medicine, University of Washington, Seattle, Washington, USA.
University of Washington · USCleveland Clinic · USMay Institute · USUniversity Hospital Leipzig · DEUniversity of Chicago · USWake Forest University · US

Funding

Vector and Transgenic Mouse CoreP30DK017047 · NIDDK · UNIVERSITY OF WASHINGTON · PI Sakeneh Zraika · 1986 to 2026
$41.4M
Structural Determinants Of Ceruloplasmin Inflammatory ActivityP01HL076491 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI PLOW, EDWARD FRANKLIN · 2004 to 2019
$27.3M
Role of Serum Amyloid A in Diabetic Vascular DiseaseP01HL092969 · NHLBI · UNIVERSITY OF WASHINGTON · PI BORNFELDT, KARIN E. · 2008 to 2019
$23.5M
CARDIOVASCULAR RESEARCH TRAINING PROGRAMT32HL007828 · NHLBI · UNIVERSITY OF WASHINGTON · PI Francis Kim, Farid Moussavi-Harami · 1997 to 2026
$10.2M
Regulation of ABCA1 functions by JAK2/STAT3 pathwayR01HL121214 · NHLBI · UNIVERSITY OF WASHINGTON · PI TANG, CHONGREN · 2014 to 2018
$2.2M
Quantitative Assessment of HDL FunctionR01HL112625 · NHLBI · UNIVERSITY OF WASHINGTON · PI HEINECKE, JAY W · 2012 to 2016
$2.1M
Cardioprotective Mechanisms of HDLR01HL108897 · NHLBI · UNIVERSITY OF WASHINGTON · PI HEINECKE, JAY W · 2012 to 2015
$1.7M
APOC3, HDL Function and Cardiovascular Complications of T1DMDP3DK108209 · NIDDK · UNIVERSITY OF WASHINGTON · PI BORNFELDT, KARIN E., HEINECKE, JAY W · 2015 to 2015
$1.6M
NHLBI NIH HHS P01 HL076491NHLBI NIH HHS P01 HL092969NHLBI NIH HHS R01 HL108897NHLBI NIH HHS R01 HL112625NHLBI NIH HHS R01 HL121214NHLBI NIH HHS T32 HL007828NIDDK NIH HHS DP3 DK108209NIDDK NIH HHS P30 DK017047
6 · The paper itself

Abstract

Using genetic and biochemical approaches, we investigated proteins that regulate macrophage cholesterol efflux capacity (CEC) and ABCA1-specific CEC (ABCA1 CEC), 2 functional assays that predict cardiovascular disease (CVD). Macrophage CEC and the concentration of HDL particles were markedly reduced in mice deficient in apolipoprotein A-I (APOA1) or apolipoprotein E (APOE) but not apolipoprotein A-IV (APOA4). ABCA1 CEC was markedly reduced in APOA1-deficient mice but was barely affected in mice deficient in APOE or APOA4. High-resolution size-exclusion chromatography of plasma produced 2 major peaks of ABCA1 CEC activity. The early-eluting peak, which coeluted with HDL, was markedly reduced in APOA1- or APOE-deficient mice. The late-eluting peak was modestly reduced in APOA1-deficient mice but little affected in APOE- or APOA4-deficient mice. Ion-exchange chromatography and shotgun proteomics suggested that plasminogen (PLG) accounted for a substantial fraction of the ABCA1 CEC activity in the peak not associated with HDL. Human PLG promoted cholesterol efflux by the ABCA1 pathway, and PLG-dependent efflux was inhibited by lipoprotein(a) [Lp(a)]. Our observations identify APOA1, APOE, and PLG as key determinants of CEC. Because PLG and Lp(a) associate with human CVD risk, interplay among the proteins might affect atherosclerosis by regulating cholesterol efflux from macrophages.

Indexed as

AtherosclerosisCholesterolEndocrinologyLipoproteinsMetabolism

Identifiers

PMID28768900
PMCPMC5543924
OpenAlexW2741358345

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.