Evidence map›Paper›PMID 21115968›Full record

ArticleJournal of lipid research2011

Biogenesis of apolipoprotein A-V and its impact on VLDL triglyceride secretion.

Anna M Blade, Melissa A Fabritius, Li Hou, Richard B Weinberg, Gregory S Shelness

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Apolipoprotein A-V is present in bile and its secretion increases with lipid absorption in Sprague-Dawley rats.American journal of physiology. Gastrointestinal and liver physiology · 2015
    Article
  11. Article
  12. Article
  13. Apolipoprotein A-V deficiency enhances chylomicron production in lymph fistula mice.American journal of physiology. Gastrointestinal and liver physiology · 2015
    Article
  14. Article
  15. Review
  16. Hyperlipoproteinemia type 3: the forgotten phenotype.Current atherosclerosis reports · 2014
    Review
  17. Article
  18. Review
  19. Influence of apolipoprotein A-V on hepatocyte lipid droplet formation.Biochemical and biophysical research communications · 2012
    Article
  20. Review
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

5 authors at 1 institution in 1 country.

Anna M BladeDepartment of Pathology, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.
Melissa A Fabritius
Li Hou
Richard B Weinberg
Gregory S Shelness
Wake Forest University · US

Funding

TISSUE CULTURE COREP01HL049373 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SHELNESS, GREGORY S · 1993 to 2012
$23.8M
STRUCTURE AND LIPID BINDING OF HUMAN APOLIPOPROTEINR01HL030897 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI WEINBERG, RICHARD B · 1987 to 2010
$2.9M
STRUCTURE AND LIPID BINDING OF HUMAN APOLIPOPROTEIN A-IVR23HL030897 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI WEINBERG, RICHARD B · 1985 to 1986
–
NHLBI NIH HHS HL-30897NHLBI NIH HHS HL-49373NHLBI NIH HHS P01 HL049373NHLBI NIH HHS R01 HL030897
6 · The paper itself

Abstract

Apolipoprotein A-V (apoA-V) is a potent regulator of intravascular triglyceride (TG) metabolism, yet its plasma concentration is very low compared with that of other apolipoproteins. To examine the basis for its low plasma concentration, the secretion efficiency of apoA-V was measured in stably transfected McA-RH7777 rat hepatoma cells. Pulse-chase experiments revealed that only ∼20% of newly synthesized apoA-V is secreted into culture medium within 3 h postsynthesis and that ∼65% undergoes presecretory turnover; similar results were obtained with transfected nonhepatic Chinese hamster ovary cells. ApoA-V secreted by McA-RH7777 cells was not associated with cell surface heparin-competable binding sites. When stably transfected McA-RH7777 cells were treated with oleic acid, the resulting increase in TG synthesis caused a reduction in apoA-V secretion, a reciprocal increase in cell-associated apoA-V, and movement of apoA-V onto cytosolic lipid droplets. In a stably transfected doxycycline-inducible McA-RH7777 cell line, apoA-V expression inhibited TG secretion by ∼50%, increased cellular TG, and reduced Z-average VLDL(1) particle diameter from 81 to 67 nm; however, no impact on apoB secretion was observed. These data demonstrate that apoA-V inefficiently traffics within the secretory pathway, that its intracellular itinerary can be regulated by changes in cellular TG accumulation, and that apoA-V synthesis can modulate VLDL TG mobilization and secretion.

Indexed as

AnimalsApolipoprotein A-VApolipoproteinsCHO CellsCricetinaeCricetulusLipoproteins, VLDLLiver Neoplasms, ExperimentalOleic AcidRatsTransfectionTriglyceridesApoa5 protein, ratApolipoprotein A-VApolipoproteinsLipoproteins, VLDLOleic AcidTriglyceridesvery low density lipoprotein triglyceride

Identifiers

PMID21115968
PMCPMC3023543
OpenAlexW2158721108

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.