Evidence map›Paper›PMID 37290445›Full record

ArticleDevelopmental cell2023

PLIN5 interacts with FATP4 at membrane contact sites to promote lipid droplet-to-mitochondria fatty acid transport.

Gregory E Miner, Christina M So, Whitney Edwards, Joey V Ragusa, Jonathan T Wine, Daniel Wong Gutierrez, Michael V Airola, Laura E Herring, Rosalind A Coleman, Eric L Klett and 1 more

Open access · greenAbstract read
In one paragraph

Article in Developmental cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
20.2field-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

96 citing papers in PubMed, 111 citations in OpenAlex.

  1. Mitophagy coordinates organelle crosstalk in health and diseases.Signal transduction and targeted therapy · 2026
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  9. Monitoring fatty acid trafficking duringbioRxiv : the preprint server for biology · 2026
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36 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

11 authors at 2 institutions in 1 country.

Gregory E MinerDepartment of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Christina M SoDepartment of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Whitney EdwardsDepartment of Biology and Genetics, McAllister Heart Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; Integrative Program for Biological and Genome Sciences, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Joey V RagusaDepartment of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Jonathan T WineDepartment of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, NY 11794, USA.
Daniel Wong GutierrezDepartment of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, NY 11794, USA.
Michael V AirolaDepartment of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, NY 11794, USA.
Laura E HerringDepartment of Pharmacology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Rosalind A ColemanDepartment of Nutrition, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Eric L KlettDepartment of Nutrition, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Sarah CohenDepartment of Cell Biology and Physiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA. Electronic address: sarahcoh@med.unc.edu.
University of North Carolina at Chapel Hill · USStony Brook University · US

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Deborah F. Tate · 1985 to 2026
$201.5M
UNIV OF NORTH CAROLINA CLINICAL NUTRITION RESEARCH UNITP30DK056350 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SUSAN M. SMITH · 1999 to 2026
$31.6M
Structure and regulation of lipid metabolism and transportR35GM128666 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI Michael Virgil Airola · 2018 to 2026
$4.0M
Molecular mechanisms of intra- and inter-cellular fatty acid traffickingR35GM133460 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Sarah Cohen · 2019 to 2026
$2.9M
IMSD at Stony Brook University: Maximizing Excellence in Research for Graduate Education -- Fostering Inclusive Research Scientist Training (FIRST)T32GM135746 · NIGMS · STATE UNIVERSITY NEW YORK STONY BROOK · PI GERGEN, JOHN PETER · 2021 to 2025
$2.3M
Mechanism of Lipid Droplet/ Mitochondria Contacts and Role of Perilipin 5 in Lipid MetabolismF32GM136027 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MINER, GREGORY · 2020 to 2021
$134k
NCI NIH HHS P30 CA016086NIDDK NIH HHS P30 DK056350NIGMS NIH HHS F32 GM136027NIGMS NIH HHS R35 GM128666NIGMS NIH HHS R35 GM133460NIGMS NIH HHS T32 GM135746
6 · The paper itself

Abstract

Cells adjust their metabolism by remodeling membrane contact sites that channel metabolites to different fates. Lipid droplet (LD)-mitochondria contacts change in response to fasting, cold exposure, and exercise. However, their function and mechanism of formation have remained controversial. We focused on perilipin 5 (PLIN5), an LD protein that tethers mitochondria, to probe the function and regulation of LD-mitochondria contacts. We demonstrate that efficient LD-to-mitochondria fatty acid (FA) trafficking and ß-oxidation during starvation of myoblasts are promoted by phosphorylation of PLIN5 and require an intact PLIN5 mitochondrial tethering domain. Using human and murine cells, we further identified the acyl-CoA synthetase, FATP4 (ACSVL4), as a mitochondrial interactor of PLIN5. The C-terminal domains of PLIN5 and FATP4 constitute a minimal protein interaction capable of inducing organelle contacts. Our work suggests that starvation leads to phosphorylation of PLIN5, lipolysis, and subsequent channeling of FAs from LDs to FATP4 on mitochondria for conversion to fatty-acyl-CoAs and subsequent oxidation.

Indexed as

Lipid DropletsPerilipin-5AnimalsCarrier ProteinsFatty AcidsFatty Acid Transport ProteinsHumansLipid MetabolismMiceMitochondriaCarrier ProteinsFatty AcidsFatty Acid Transport ProteinsPerilipin-5SLC27A4 protein, humanSlc27a4 protein, mouseacyl-CoAFATP4fatty acidslipid dropletsmembrane contact sitesmetabolismmitochondriaorganellesPLIN5

Identifiers

PMID37290445
PMCPMC10525032
OpenAlexW4379618280

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.