Evidence map›Paper›PMID 38984997›Full record

ArticleFunction (Oxford, England)2024

The P2X7 Receptor is a Master Regulator of Microparticle and Mitochondria Exchange in Mouse Microglia.

Simonetta Falzoni, Valentina Vultaggio-Poma, Paola Chiozzi, Mario Tarantini, Elena Adinolfi, Paola Boldrini, Anna Lisa Giuliani, Giampaolo Morciano, Yong Tang, Dariusz C Gorecki and 1 more

Abstract read
In one paragraph

Article in Function (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 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

11 authors.

Simonetta FalzoniDepartment of Medical Sciences, University of Ferrara, 44100 Ferrara, Italy.
Valentina Vultaggio-PomaDepartment of Medical Sciences, University of Ferrara, 44100 Ferrara, Italy.
Paola ChiozziDepartment of Medical Sciences, University of Ferrara, 44100 Ferrara, Italy.
Mario TarantiniDepartment of Medical Sciences, University of Ferrara, 44100 Ferrara, Italy.
Elena AdinolfiDepartment of Medical Sciences, University of Ferrara, 44100 Ferrara, Italy.
Paola BoldriniCenter for Electron Microscopy, University of Ferrara, 44100 Ferrara, Italy.
Anna Lisa GiulianiDepartment of Medical Sciences, University of Ferrara, 44100 Ferrara, Italy.
Giampaolo MorcianoDepartment of Medical Sciences, University of Ferrara, 44100 Ferrara, Italy.
Yong TangInternational Joint Research Centre on Purinergic Signalling & Chengdu University of Traditional Chinese Medicine, 610075 Chengdu, China.
Dariusz C GoreckiSchool of Pharmacy and Biomedical Sciences, University of Portsmouth, P01 2DT Portsmouth, UK.ORCID 0000-0003-3584-1654
Francesco Di VirgilioDepartment of Medical Sciences, University of Ferrara, 44100 Ferrara, Italy.ORCID 0000-0003-3566-1362

Funding

European Cooperation in Science and TechnologyItalian Association for Cancer Research IG 18581Ministry of Education of Italy 20178YTNWCRoyal Society Exchange Fellowship IES\R3\170196
6 · The paper itself

Abstract

Microparticles (MPs) are secreted by all cells, where they play a key role in intercellular communication, differentiation, inflammation, and cell energy transfer. P2X7 receptor (P2X7R) activation by extracellular ATP (eATP) causes a large MP release and affects their contents in a cell-specific fashion. We investigated MP release and functional impact in microglial cells from P2X7R-WT or P2X7R-KO mice, as well as mouse microglial cell lines characterized for high (N13-P2X7RHigh) or low (N13-P2X7RLow) P2X7R expression. P2X7R stimulation promoted release of a mixed MP population enriched with naked mitochondria. Released mitochondria were taken up and incorporated into the mitochondrial network of the recipient cells in a P2X7R-dependent fashion. NLRP3 and the P2X7R itself were also delivered to the recipient cells. Microparticle transfer increased the energy level of the recipient cells and conferred a pro-inflammatory phenotype. These data show that the P2X7R is a master regulator of intercellular organelle and MP trafficking in immune cells.

Indexed as

Cell-Derived MicroparticlesMice, KnockoutMicrogliaMitochondriaReceptors, Purinergic P2X7Adenosine TriphosphateAnimalsCell LineMiceNLR Family, Pyrin Domain-Containing 3 ProteinAdenosine TriphosphateNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseP2rx7 protein, mouseReceptors, Purinergic P2X7inflammationmicrogliamicroparticlesmitochondriaP2X7 receptor

Identifiers

PMID38984997
PMCPMC11237899

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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.