Evidence map›Paper›PMID 30199545›Full record

ArticlePLoS genetics2018

Physiological and pathological roles of FATP-mediated lipid droplets in Drosophila and mice retina.

Daan M Van Den Brink, Aurélie Cubizolle, Gilles Chatelain, Nathalie Davoust, Victor Girard, Simone Johansen, Francesco Napoletano, Pierre Dourlen, Laurent Guillou, Claire Angebault-Prouteau and 4 more

Abstract read
In one paragraph

Article in PLoS genetics, 2018. 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
–field-weighted citation impact
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.

  1. Review
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  17. Article
  18. Adaptive and maladaptive roles of lipid droplets in health and disease.American journal of physiology. Cell physiology · 2022
    Review
  19. Review
  20. Functions of Stress-Induced Lipid Droplets in the Nervous System.Frontiers in cell and developmental biology · 2022
    Review
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

14 authors.

Daan M Van Den BrinkUniversité de Lyon, ENSL, UCBL, CNRS, LBMC, UMS 3444 Biosciences Lyon Gerland, Lyon, France.
Aurélie CubizolleInstitut des Neurosciences de Montpellier, INSERM U1051, CHU St Eloi, Montpellier, France.
Gilles ChatelainUniversité de Lyon, ENSL, UCBL, CNRS, LBMC, UMS 3444 Biosciences Lyon Gerland, Lyon, France.ORCID 0000-0003-0364-4541
Nathalie DavoustUniversité de Lyon, ENSL, UCBL, CNRS, LBMC, UMS 3444 Biosciences Lyon Gerland, Lyon, France.
Victor GirardUniversité de Lyon, ENSL, UCBL, CNRS, LBMC, UMS 3444 Biosciences Lyon Gerland, Lyon, France.
Simone JohansenUniversité de Lyon, ENSL, UCBL, CNRS, LBMC, UMS 3444 Biosciences Lyon Gerland, Lyon, France.ORCID 0000-0002-6140-9366
Francesco NapoletanoMolecular Oncology Unit, Department of Life Sciences, University of Trieste c/o Laboratorio Nazionale CIB, Area Science Park, Trieste, Italy.ORCID 0000-0002-0910-3167
Pierre DourlenInstitut Pasteur de Lille; Inserm, U1167, RID-AGE-Risk Factors and Molecular Determinants of Aging-Related Diseases; University Lille, U1167-Excellence Laboratory LabEx DISTALZ, Lille, France.
Laurent GuillouInstitut des Neurosciences de Montpellier, INSERM U1051, CHU St Eloi, Montpellier, France.
Claire Angebault-ProuteauInstitut des Neurosciences de Montpellier, INSERM U1051, CHU St Eloi, Montpellier, France.
Nathalie Bernoud-HubacUniv Lyon, CarMeN laboratory, INSA Lyon, INSERM U1060, INRA U1397, Université Claude Bernard Lyon 1, F-69621, Villeurbanne, France.
Michel GuichardantUniv Lyon, CarMeN laboratory, INSA Lyon, INSERM U1060, INRA U1397, Université Claude Bernard Lyon 1, F-69621, Villeurbanne, France.
Philippe BrabetInstitut des Neurosciences de Montpellier, INSERM U1051, CHU St Eloi, Montpellier, France.ORCID 0000-0003-2739-1622
Bertrand MollereauUniversité de Lyon, ENSL, UCBL, CNRS, LBMC, UMS 3444 Biosciences Lyon Gerland, Lyon, France.ORCID 0000-0003-4710-8185

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
NIH HHS P40 OD018537
6 · The paper itself

Abstract

Increasing evidence suggests that dysregulation of lipid metabolism is associated with neurodegeneration in retinal diseases such as age-related macular degeneration and in brain disorders such as Alzheimer's and Parkinson's diseases. Lipid storage organelles (lipid droplets, LDs), accumulate in many cell types in response to stress, and it is now clear that LDs function not only as lipid stores but also as dynamic regulators of the stress response. However, whether these LDs are always protective or can also be deleterious to the cell is unknown. Here, we investigated the consequences of LD accumulation on retinal cell homeostasis under physiological and stress conditions in Drosophila and in mice. In wild-type Drosophila, we show that dFatp is required and sufficient for expansion of LD size in retinal pigment cells (RPCs) and that LDs in RPCs are required for photoreceptor survival during aging. Similarly, in mice, LD accumulation induced by RPC-specific expression of human FATP1 was non-toxic and promoted mitochondrial energy metabolism in RPCs and non-autonomously in photoreceptor cells. In contrast, the inhibition of LD accumulation by dFatp knockdown suppressed neurodegeneration in Aats-metFB Drosophila mutants, which carry elevated levels of reactive oxygen species (ROS). This suggests that abnormal turnover of LD may be toxic for photoreceptors cells of the retina under oxidative stress. Collectively, these findings indicate that FATP-mediated LD formation in RPCs promotes RPC and neuronal homeostasis under physiological conditions but could be deleterious for the photoreceptors under pathological conditions.

Indexed as

AgingAnimalsAnimals, Genetically ModifiedCoenzyme A LigasesDrosophilaDrosophila ProteinsEnergy MetabolismFatty Acid Transport ProteinsLipid DropletsLipid MetabolismMiceMice, Inbred C57BLMitochondriaOxidative StressReactive Oxygen SpeciesRetinaCoenzyme A LigasesDrosophila ProteinsFatp1 protein, DrosophilaFatty Acid Transport ProteinsReactive Oxygen SpeciesSLC27A1 protein, human

Identifiers

PMID30199545
PMCPMC6147681

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Registered trials

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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.