Evidence map›Paper›PMID 22367708›Full record

ArticleHepatology (Baltimore, Md.)2012

Liver phospholipid transfer protein (PLTP) expression with a PLTP-null background promotes very low-density lipoprotein production in mice.

Amirfarbod Yazdanyar, Xian-Cheng Jiang

Open access · greenAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

31 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Intracellular Cholesterol Trafficking.Cold Spring Harbor perspectives in biology · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Sphingolipids and Cholesterol.Advances in experimental medicine and biology · 2022
    Article
  11. Liver X receptors and liver physiology.Biochimica et biophysica acta. Molecular basis of disease · 2021
    Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Amirfarbod YazdanyarDepartment of Cell Biology, SUNY Downstate Medical Center, Brooklyn, NY 11203, USA.
Xian-Cheng Jiang
SUNY Downstate Health Sciences University · US

Funding

The role of PLTP in BLp metabolism and atherogenesisR01HL069817 · NHLBI · SUNY DOWNSTATE MEDICAL CENTER · PI JIANG, XIAN-CHENG · 2002 to 2010
$2.6M
NHLBI NIH HHS HL69817NHLBI NIH HHS R01 HL069817
6 · The paper itself

Abstract

unlabelledIt is known that plasma phospholipid transfer protein (PLTP) activity influences lipoprotein metabolism. The liver is one of the major sites of lipoprotein production and degradation, as well as of PLTP expression. To address the impact of liver-expressed PLTP on lipoprotein metabolism, we created a mouse model that expresses PLTP in the liver acutely and specifically, with a PLTP-null background. This approach in mouse model preparations can also be used universally for evaluating the function of many other genes in the liver. We found that liver PLTP expression dramatically increases plasma levels of non-high-density lipoprotein (HDL) cholesterol (2.7-fold, P < 0.0001), non-HDL phospholipid (2.5-fold, P < 0.001), and triglyceride (51%, P < 0.01), but has no significant influence on plasma HDL lipids compared with controls. Plasma apolipoprotein (apo)B levels were also significantly increased in PLTP-expressing mice (2.2-fold, P < 0.001), but those of apoA-I were not. To explore the mechanism involved, we examined the lipidation and secretion of nascent very low-density lipoprotein (VLDL), finding that liver PLTP expression significantly increases VLDL lipidation in hepatocyte microsomal lumina, and also VLDL secretion into the plasma.

conclusionIt is possible to prepare a mouse model that expresses the gene of interest only in the liver, but not in other tissues. Our results suggest, for the first time, that the major function of liver PLTP is to drive VLDL production and makes a small contribution to plasma PLTP activity.

Indexed as

AnimalsApolipoproteins BCarbon RadioisotopesCholesterol, HDLCholesterol, VLDLGene ExpressionGreen Fluorescent ProteinsHeterozygoteLipoproteins, HDLLipoproteins, VLDLLiverMiceMice, Inbred C57BLMice, KnockoutMicrosomes, LiverPhospholipid Transfer ProteinsApolipoproteins BCarbon RadioisotopesCholesterol, HDLCholesterol, VLDLGreen Fluorescent ProteinsLipoproteins, HDLLipoproteins, VLDLphospholipid transfer protein, mousePhospholipid Transfer ProteinsSulfur RadioisotopesTriglycerides

Identifiers

PMID22367708
PMCPMC3409695
OpenAlexW2054117608

What OpenQuestion holds

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LicenceTDM
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.