Evidence map›Paper›PMID 41709222›Full record

ArticleCell communication and signaling : CCS2026

Free fatty acid receptor 2 allosterism is defined by cellular context.

Simon Lind, Ayaan Abdi Ali, Sarah Al Hamoud Al Asswad, Volker M Lauschke, Huamei Forsman, Claes Dahlgren, Linda C Johansson

Abstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Simon LindDepartment of Medical Biochemistry and Cell biology, Institute of Biomedicine, Gothenburg University, Gothenburg, Sweden. Simon.lind@gu.se.
Ayaan Abdi AliDepartment of Medical Biochemistry and Cell biology, Institute of Biomedicine, Gothenburg University, Gothenburg, Sweden.
Sarah Al Hamoud Al AsswadDepartment of Medical Biochemistry and Cell biology, Institute of Biomedicine, Gothenburg University, Gothenburg, Sweden.
Volker M LauschkeDepartment of Physiology & Pharmacology, Section for Personalized Medicine and Drug Development, Karolinska Institutet, Stockholm, Sweden.
Huamei ForsmanDepartment of Rheumatology and Inflammation Research, Gothenburg University, Gothenburg, Sweden.
Claes DahlgrenDepartment of Rheumatology and Inflammation Research, Gothenburg University, Gothenburg, Sweden.
Linda C JohanssonDepartment of Medical Biochemistry and Cell biology, Institute of Biomedicine, Gothenburg University, Gothenburg, Sweden. linda.johansson.4@gu.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAllosteric modulators offer a way to fine-tune GPCR signaling in the presence of endogenous ligands. The short-chain fatty acid receptor FFA2R (GPR43) recognizes propionate and allosteric ligands such as Cmp58 and AZ1729. We characterized FFA2R signaling and allosteric modulation using multiple cell models including HEK293, HL60 cells and primary human neutrophils.

methodsFFA2R activation was assessed using complementary assays in HEK293 and HL60 cells as well as primary human neutrophils. G protein activation and β-arrestin recruitment were profiled using ebBRET biosensors. Ca

resultsPropionate activated all tested G proteins except Gα

conclusionsAcross systems, Ca²⁺ mobilization emerged as a conserved, receptor-proximal output of FFA2R, while allosteric modulation by Cmp58 and AZ1729 promoted Gα

Indexed as

Receptors, G-Protein-CoupledAllosteric Regulationbeta-ArrestinsCalciumHEK293 CellsHL-60 CellsHumansNeutrophilsPeptides, CyclicReactive Oxygen SpeciesSignal Transductionbeta-ArrestinsCalciumFFAR2 protein, humanPeptides, CyclicReactive Oxygen SpeciesReceptors, G-Protein-CoupledYM-254890Allosteric activationAllosteric modulationCa2+ mobilizationFFA2RFunctional selectivityGPR43HEK293HL60NeutrophilsReactive oxygen species

Identifiers

PMID41709222
PMCPMC12930632

What OpenQuestion 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 OpenQuestion graph.