Evidence map›Paper›PMID 34165498›Full record

ReviewThe Journal of cell biology2021

Lipid droplets and the host-pathogen dynamic: FATal attraction?

Marta Bosch, Matthew J Sweet, Robert G Parton, Albert Pol

Abstract readReview
In one paragraph

Review in The Journal of cell biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed.

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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

4 authors.

Marta BoschLipid Trafficking and Disease Group, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain.
Matthew J SweetInstitute for Molecular Bioscience, University of Queensland, Brisbane, Australia.ORCID 0000-0002-0406-8139
Robert G PartonInstitute for Molecular Bioscience, University of Queensland, Brisbane, Australia.ORCID 0000-0002-7494-5248
Albert PolLipid Trafficking and Disease Group, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain.ORCID 0000-0002-1750-1085

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the ongoing conflict between eukaryotic cells and pathogens, lipid droplets (LDs) emerge as a choke point in the battle for nutrients. While many pathogens seek the lipids stored in LDs to fuel an expensive lifestyle, innate immunity rewires lipid metabolism and weaponizes LDs to defend cells and animals. Viruses, bacteria, and parasites directly and remotely manipulate LDs to obtain substrates for metabolic energy, replication compartments, assembly platforms, membrane blocks, and tools for host colonization and/or evasion such as anti-inflammatory mediators, lipoviroparticles, and even exosomes. Host LDs counterattack such advances by synthesizing bioactive lipids and toxic nucleotides, organizing immune signaling platforms, and recruiting a plethora of antimicrobial proteins to provide a front-line defense against the invader. Here, we review the current state of this conflict. We will discuss why, when, and how LDs efficiently coordinate and precisely execute a plethora of immune defenses. In the age of antimicrobial resistance and viral pandemics, understanding innate immune strategies developed by eukaryotic cells to fight and defeat dangerous microorganisms may inform future anti-infective strategies.

Indexed as

Energy MetabolismImmunity, InnateAnimalsAntimicrobial Cationic PeptidesBacteriaEvolution, MolecularHost-Pathogen InteractionsHumansLipid DropletsParasitesSignal TransductionVirusesAntimicrobial Cationic Peptides

Identifiers

PMID34165498
PMCPMC8240858

What Socratic holds

Textmetadata
LicenceCC BY-NC-SA
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 Socratic graph.