Evidence map›Paper›PMID 17200715›Full record

ArticleThe Journal of clinical investigation2007

Liver heparan sulfate proteoglycans mediate clearance of triglyceride-rich lipoproteins independently of LDL receptor family members.

Jennifer M MacArthur, Joseph R Bishop, Kristin I Stanford, Lianchun Wang, André Bensadoun, Joseph L Witztum, Jeffrey D Esko

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed, 1 pooled it
9.5field-weighted citation impact, top 1% 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

107 citing papers in PubMed, 1 synthesis or guideline pooled it, 211 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  7. Review
  8. Article
  9. Article
  10. Article
  11. Bruch's membrane heparan sulfate retains lipoproteins in the early stages of age-related macular degeneration.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Review
  13. Tale of 2 Receptors.Arteriosclerosis, thrombosis, and vascular biology · 2025
    Article
  14. Review
  15. Article
  16. Review
  17. Apolipoprotein C3: form begets function.Journal of lipid research · 2024
    Review
  18. Review
  19. Protective Effects ofInternational journal of molecular sciences · 2023
    Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Jennifer M MacArthurBiomedical Sciences Graduate Program, University of California, San Diego, La Jolla, California 92093-0687, USA.
Joseph R Bishop
Kristin I Stanford
Lianchun Wang
André Bensadoun
Joseph L Witztum
Jeffrey D Esko
University of California, San Diego · USCornell University · US

Funding

Siglec Modulation of Inflammation in Humans and MiceP01HL057345 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI VARKI, NISSI MARY · 1997 to 2012
$24.1M
SCOR IN MOLECULAR MEDICINE AND ATHEROSCLEROSISP50HL056989 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI QUEHENBERGER, OSWALD · 1997 to 2006
$14.1M
GENETIC CONTROL OF PROTEOGLYCAN METABOLISMR37GM033063 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ESKO, JEFFREY D · 2000 to 2010
$3.9M
LIPID METABOLISM IN ANIMAL CELLSR01GM033063 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ESKO, JEFFREY D · 1985 to 2019
$3.4M
NHLBI NIH HHS HL56989NHLBI NIH HHS HL57345NHLBI NIH HHS P01 HL057345NHLBI NIH HHS P50 HL056989NIGMS NIH HHS GM33063NIGMS NIH HHS R01 GM033063NIGMS NIH HHS R37 GM033063
6 · The paper itself

Abstract

We examined the role of hepatic heparan sulfate in triglyceride-rich lipoprotein metabolism by inactivating the biosynthetic gene GlcNAc N-deacetylase/N-sulfotransferase 1 (Ndst1) in hepatocytes using the Cre-loxP system, which resulted in an approximately 50% reduction in sulfation of liver heparan sulfate. Mice were viable and healthy, but they accumulated triglyceride-rich lipoprotein particles containing apoB-100, apoB-48, apoE, and apoCI-IV. Compounding the mutation with LDL receptor deficiency caused enhanced accumulation of both cholesterol- and triglyceride-rich particles compared with mice lacking only LDL receptors, suggesting that heparan sulfate participates in the clearance of cholesterol-rich lipoproteins as well. Mutant mice synthesized VLDL normally but showed reduced plasma clearance of human VLDL and a corresponding reduction in hepatic VLDL uptake. Retinyl ester excursion studies revealed that clearance of intestinally derived lipoproteins also depended on hepatocyte heparan sulfate. These findings show that under normal physiological conditions, hepatic heparan sulfate proteoglycans play a crucial role in the clearance of both intestinally derived and hepatic lipoprotein particles.

Indexed as

Apolipoproteins EFibroblast Growth Factor 2Heparan Sulfate ProteoglycansHepatocytesHumansHypertriglyceridemiaLipoproteinsLiverReceptors, LDLTriglyceridesApolipoproteins EFibroblast Growth Factor 2Heparan Sulfate ProteoglycansLipoproteinsReceptors, LDLTriglycerides

Identifiers

PMID17200715
PMCPMC1716206
OpenAlexW2157280645

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.