Evidence map›Paper›PMID 39497825›Full record

ArticleFrontiers in immunology2024

Analysis of lipid uptake, storage, and fatty acid oxidation by group 2 innate lymphoid cells.

Audrey Roy-Dorval, Rebecca C Deagle, Frederik Roth, Mathilde Raybaud, Nailya Ismailova, Sai Sakktee Krisna, Damon G K Aboud, Camille Stegen, Julien Leconte, Gabriel Berberi and 2 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
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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

12 authors.

Audrey Roy-Dorval *Department of Microbiology and Immunology, McGill University, Montréal, QC, Canada.
Rebecca C Deagle *Department of Microbiology and Immunology, McGill University, Montréal, QC, Canada.
Frederik RothDepartment of Microbiology and Immunology, McGill University, Montréal, QC, Canada.
Mathilde RaybaudDepartment of Microbiology and Immunology, McGill University, Montréal, QC, Canada.
Nailya IsmailovaDepartment of Microbiology and Immunology, McGill University, Montréal, QC, Canada.
Sai Sakktee KrisnaMcGill University Research Center on Complex Traits (MRCCT), McGill University, Montréal, QC, Canada.
Damon G K AboudDepartment of Chemical Engineering, McGill University, Montréal, QC, Canada.
Camille StegenDepartment of Microbiology and Immunology, McGill University, Montréal, QC, Canada.
Julien LeconteDepartment of Microbiology and Immunology, McGill University, Montréal, QC, Canada.
Gabriel BerberiDepartment of Microbiology and Immunology, McGill University, Montréal, QC, Canada.
Ademola EsomojumiDepartment of Microbiology and Immunology, McGill University, Montréal, QC, Canada.
Jörg H FritzDepartment of Microbiology and Immunology, McGill University, Montréal, QC, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Group 2 Innate Lymphoid Cells (ILC2) are critical drivers of both innate and adaptive type 2 immune responses, known to orchestrate processes involved in tissue restoration and wound healing. In addition, ILC2 have been implicated in chronic inflammatory barrier disorders in type 2 immunopathologies such as allergic rhinitis and asthma. ILC2 in the context of allergen-driven airway inflammation have recently been shown to influence local and systemic metabolism, as well as being rich in lipid-storing organelles called lipid droplets. However, mechanisms of ILC2 lipid anabolism and catabolism remain largely unknown and the impact of these metabolic processes in regulating ILC2 phenotypes and effector functions has not been extensively characterized. ILC2 phenotypes and effector functions are shaped by their metabolic status, and determining the metabolic requirements of ILC2 is critical in understanding their role in type 2 immune responses and their associated pathophysiology. We detail here a novel experimental method of implementing flow cytometry for large scale analysis of fatty acid uptake, storage of neutral lipids, and fatty acid oxidation in primary murine ILC2 with complementary morphological analysis of lipid storage using confocal microscopy. By combining flow cytometry and confocal microscopy, we can identify the metabolic lipid requirements for ILC2 functions as well as characterize the phenotype of lipid storage in ILC2. Linking lipid metabolism pathways to ILC2 phenotypes and effector functions is critical for the assessment of novel pharmaceutical strategies to regulate ILC2 functions in type 2 immunopathologies.

Indexed as

Fatty AcidsImmunity, InnateLipid MetabolismLymphocytesOxidation-ReductionAnimalsCells, CulturedFlow CytometryMiceMice, Inbred C57BLFatty Acidsfatty acid oxidation (FAO)fatty acid uptakeflow cytometrygroup 2 innate lymphoid cells (ILC2)immunometabolismlipid dropletsmicroscopytype 2 immunity

Identifiers

PMID39497825
PMCPMC11532145

What Socratic holds

Textmetadata
LicenceCC BY
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.