Evidence map›Paper›PMID 22511767›Full record

ArticleThe Journal of biological chemistry2012

Lysophosphatidylcholine acyltransferase 3 knockdown-mediated liver lysophosphatidylcholine accumulation promotes very low density lipoprotein production by enhancing microsomal triglyceride transfer protein expression.

Zhiqiang Li, Tingbo Ding, Xiaoyue Pan, Yan Li, Ruohan Li, Philip E Sanders, Ming-Shang Kuo, M Mahmood Hussain, Guoqing Cao, Xian-Cheng Jiang

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. 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
2.3field-weighted citation impact, top 13% 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, 55 citations in OpenAlex.

  1. Article
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  11. Article
  12. Translational cancer research · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Liver X receptors and liver physiology.Biochimica et biophysica acta. Molecular basis of disease · 2021
    Review
  17. The interaction between brain and liver regulates lipid metabolism in the TBI pathology.Biochimica et biophysica acta. Molecular basis of disease · 2021
    Article
  18. Review
  19. Article
  20. Hepatic gap junctions amplify alcohol liver injury by propagating cGAS-mediated IRF3 activation.Proceedings of the National Academy of Sciences of the United States of America · 2020
    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

10 authors at 3 institutions in 2 countries.

Zhiqiang LiMolecular and Cellular Cardiology Program, Veterans Affairs New York Harbor Healthcare System, Brooklyn, New York 11209, USA.
Tingbo Ding
Xiaoyue Pan
Yan Li
Ruohan Li
Philip E Sanders
Ming-Shang Kuo
M Mahmood Hussain
Guoqing Cao
Xian-Cheng Jiang
SUNY Downstate Health Sciences University · USEli Lilly (United States) · USVA NY Harbor Healthcare System · US

Funding

Diurnal regulation of MTP and plasma lipidsR01DK081879 · NIDDK · SUNY DOWNSTATE MEDICAL CENTER · PI HUSSAIN, M MAHMOOD · 2009 to 2014
$2.3M
The effect of macrophage sphingomyelin synthase (SMS) on atherosclerosisR01HL093419 · NHLBI · SUNY DOWNSTATE MEDICAL CENTER · PI JIANG, XIAN-CHENG · 2009 to 2010
$853k
NHLBI NIH HHS HL093419NHLBI NIH HHS R01 HL093419NIDDK NIH HHS R01 DK081879
6 · The paper itself

Abstract

After de novo biosynthesis phospholipids undergo extensive remodeling by the Lands' cycle. Enzymes involved in phospholipid biosynthesis have been studied extensively but not those involved in reacylation of lysophosphopholipids. One key enzyme in the Lands' cycle is fatty acyl-CoA:lysophosphatidylcholine acyltransferase (LPCAT), which utilizes lysophosphatidylcholine (LysoPC) and fatty acyl-CoA to produce various phosphatidylcholine (PC) species. Four isoforms of LPCAT have been identified. In this study we found that LPCAT3 is the major hepatic isoform, and its knockdown significantly reduces hepatic LPCAT activity. Moreover, we report that hepatic LPCAT3 knockdown increases certain species of LysoPCs and decreases certain species of PC. A surprising observation was that LPCAT3 knockdown significantly reduces hepatic triglycerides. Despite this, these mice had higher plasma triglyceride and apoB levels. Lipoprotein production studies indicated that reductions in LPCAT3 enhanced assembly and secretion of triglyceride-rich apoB-containing lipoproteins. Furthermore, these mice had higher microsomal triglyceride transfer protein (MTP) mRNA and protein levels. Mechanistic studies in hepatoma cells revealed that LysoPC enhances secretion of apoB but not apoA-I in a concentration-dependent manner. Moreover, LysoPC increased MTP mRNA, protein, and activity. In short, these results indicate that hepatic LPCAT3 modulates VLDL production by regulating LysoPC levels and MTP expression.

Indexed as

1-Acylglycerophosphocholine O-AcyltransferaseAnimalsApolipoprotein A-IApolipoprotein B-100Apolipoproteins BCarrier ProteinsGene Expression RegulationGene Knockdown TechniquesLipoproteins, VLDLLiverLysophosphatidylcholinesMaleMiceProtein BiosynthesisRNA, MessengerTriglycerides1-Acylglycerophosphocholine O-AcyltransferaseApob protein, mouseApolipoprotein A-IApolipoprotein B-100Apolipoproteins BCarrier ProteinsLipoproteins, VLDLLysophosphatidylcholinesmicrosomal triglyceride transfer proteinRNA, MessengerTriglycerides

Identifiers

PMID22511767
PMCPMC3370195
OpenAlexW1968642527

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.