Evidence map›Paper›PMID 30379616›Full record

ReviewAnnual review of physiology2019

Phospholipid Remodeling in Physiology and Disease.

Bo Wang, Peter Tontonoz

Open access · greenAbstract readReview
In one paragraph

Review in Annual review of physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 275 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
275citing papers in PubMed, 1 pooled it
16.6field-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

275 citing papers in PubMed, 1 synthesis or guideline pooled it, 499 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  17. Lipid-Enriched Diet Advances Early Oocyte Development in the EndangeredAnimals : an open access journal from MDPI · 2026
    Article
  18. Article
  19. Article
  20. Review

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

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

2 authors at 1 institution in 1 country.

Bo WangDepartment of Pathology and Laboratory Medicine, Molecular Biology Institute, David Geffen School of Medicine, University of California, Los Angeles, California 90272, USA; email: ptontonoz@mednet.ucla.edu.
Peter TontonozDepartment of Pathology and Laboratory Medicine, Molecular Biology Institute, David Geffen School of Medicine, University of California, Los Angeles, California 90272, USA; email: ptontonoz@mednet.ucla.edu.
University of California, Los Angeles · US

Funding

The Role of Lpcat3 and Phospholipid Remodeling in Intestinal HomeostasisK01DK114373 · NIDDK · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI WANG, BO · 2018 to 2022
$769k
NIDDK NIH HHS K01 DK114373
6 · The paper itself

Abstract

Phospholipids are major constituents of biological membranes. The fatty acyl chain composition of phospholipids determines the biophysical properties of membranes and thereby affects their impact on biological processes. The composition of fatty acyl chains is also actively regulated through a deacylation and reacylation pathway called Lands' cycle. Recent studies of mouse genetic models have demonstrated that lysophosphatidylcholine acyltransferases (LPCATs), which catalyze the incorporation of fatty acyl chains into the sn-2 site of phosphatidylcholine, play important roles in pathophysiology. Two LPCAT family members, LPCAT1 and LPCAT3, have been particularly well studied. LPCAT1 is crucial for proper lung function due to its role in pulmonary surfactant biosynthesis. LPCAT3 maintains systemic lipid homeostasis by regulating lipid absorption in intestine, lipoprotein secretion, and de novo lipogenesis in liver. Mounting evidence also suggests that changes in LPCAT activity may be potentially involved in pathological conditions, including nonalcoholic fatty liver disease, atherosclerosis, viral infections, and cancer. Pharmacological manipulation of LPCAT activity and membrane phospholipid composition may provide new therapeutic options for these conditions.

Indexed as

1-Acylglycerophosphocholine O-AcyltransferaseAnimalsDiseaseHomeostasisHumansLiverPhospholipidsSignal Transduction1-Acylglycerophosphocholine O-AcyltransferasePhospholipidscholesterol metabolismintestinal homeostasislipid metabolismlipogenesislipoprotein productionlysophosphatidylcholine acyltransferasephospholipid remodelingsurfactant biosynthesis

Identifiers

PMID30379616
PMCPMC7008953
OpenAlexW2899384460

What OpenQuestion holds

Textmetadata
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.