Evidence map›Paper›PMID 28846071›Full record

ArticleThe Journal of clinical investigation2017

ER phospholipid composition modulates lipogenesis during feeding and in obesity.

Xin Rong, Bo Wang, Elisa Nd Palladino, Thomas Q de Aguiar Vallim, David A Ford, Peter Tontonoz

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 91 citations in OpenAlex.

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  13. Methyltransferase Setd2 prevents T cell-mediated autoimmune diseases via phospholipid remodeling.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  17. Hepatic Phospholipid Remodeling Modulates Insulin Sensitivity and Systemic Metabolism.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
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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

6 authors at 3 institutions in 1 country.

Xin RongDepartment of Pathology and Laboratory Medicine, Department of Medicine, UCLA, Los Angeles, California, USA.
Bo WangDepartment of Pathology and Laboratory Medicine, Department of Medicine, UCLA, Los Angeles, California, USA.
Elisa Nd PalladinoDepartment of Biochemistry and Molecular Biology, and Center for Cardiovascular Research, Saint Louis University, St. Louis, Missouri, USA.
Thomas Q de Aguiar VallimDivision of Cardiology, Department of Medicine.
David A FordDepartment of Biochemistry and Molecular Biology, and Center for Cardiovascular Research, Saint Louis University, St. Louis, Missouri, USA.
Peter TontonozDepartment of Pathology and Laboratory Medicine, Department of Medicine, UCLA, Los Angeles, California, USA.
Saint Louis University · USUniversity of California, Los Angeles · USHoward Hughes Medical Institute · US

Funding

ULTRASTRUCTURE OF THE INTIMA IN EARLY LESION FORMATIONP01HL030568 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI FOGELMAN, ALAN M · 1985 to 2019
$55.2M
Transgenic & Knock-out MouseP30DK063491 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PETER J TONTONOZ · 2003 to 2026
$40.4M
Pilot and Feasibility ProgramP30DK041301 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1990 to 2019
$18.0M
Regulation of SREBP-1 Processing Lipogenesis by LPCATF32DK109601 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WANG, BO · 2016 to 2017
$100k
NHLBI NIH HHS P01 HL030568NIDDK NIH HHS F32 DK109601NIDDK NIH HHS P30 DK041301NIDDK NIH HHS P30 DK063491
6 · The paper itself

Abstract

Sterol regulatory element-binding protein 1c (SREBP-1c) is a central regulator of lipogenesis whose activity is controlled by proteolytic cleavage. The metabolic factors that affect its processing are incompletely understood. Here, we show that dynamic changes in the acyl chain composition of ER phospholipids affect SREBP-1c maturation in physiology and disease. The abundance of polyunsaturated phosphatidylcholine in liver ER is selectively increased in response to feeding and in the setting of obesity-linked insulin resistance. Exogenous delivery of polyunsaturated phosphatidylcholine to ER accelerated SREBP-1c processing through a mechanism that required an intact SREBP cleavage-activating protein (SCAP) pathway. Furthermore, induction of the phospholipid-remodeling enzyme LPCAT3 in response to liver X receptor (LXR) activation promoted SREBP-1c processing by driving the incorporation of polyunsaturated fatty acids into ER. Conversely, LPCAT3 deficiency increased membrane saturation, reduced nuclear SREBP-1c abundance, and blunted the lipogenic response to feeding, LXR agonist treatment, or obesity-linked insulin resistance. Desaturation of the ER membrane may serve as an auxiliary signal of the fed state that promotes lipid synthesis in response to nutrient availability.

Indexed as

Insulin ResistanceLipogenesis1-Acylglycerophosphocholine O-AcyltransferaseAnimalsEndoplasmic ReticulumIntracellular Signaling Peptides and ProteinsLiver X ReceptorsMembrane ProteinsMiceMice, TransgenicObesityPhospholipidsSterol Regulatory Element Binding Protein 11-Acylglycerophosphocholine O-AcyltransferaseIntracellular Signaling Peptides and ProteinsLiver X ReceptorsLPCAT3 protein, mouseMembrane ProteinsPhospholipidsSrebf1 protein, mouseSREBP cleavage-activating proteinSterol Regulatory Element Binding Protein 1

Identifiers

PMID28846071
PMCPMC5617651
OpenAlexW2747598946

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.