Evidence map›Paper›PMID 40643469›Full record

ArticleCells2025

Effects of Selective α7 Nicotinic Acetylcholine Receptor Stimulation in Oligodendrocytes: Putative Implication in Neuroinflammation.

Claudia Guerriero, Giulia Puliatti, Tamara Di Marino, Giulia Scanavino, Carlo Matera, Clelia Dallanoce, Ada Maria Tata

Abstract read
In one paragraph

Article in Cells, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Claudia GuerrieroDepartment of Biology and Biotechnologies, Sapienza University of Rome, Piazzale A. Moro 5, 00185 Rome, Italy.
Giulia PuliattiDepartment of Biology and Biotechnologies, Sapienza University of Rome, Piazzale A. Moro 5, 00185 Rome, Italy.ORCID 0000-0002-9275-4576
Tamara Di MarinoDepartment of Biology and Biotechnologies, Sapienza University of Rome, Piazzale A. Moro 5, 00185 Rome, Italy.
Giulia ScanavinoDepartment of Biology and Biotechnologies, Sapienza University of Rome, Piazzale A. Moro 5, 00185 Rome, Italy.ORCID 0009-0004-7685-8326
Carlo MateraDepartment of Pharmaceutical Sciences, University of Milan, 20133 Milan, Italy.ORCID 0000-0001-6939-3859
Clelia DallanoceDepartment of Pharmaceutical Sciences, University of Milan, 20133 Milan, Italy.ORCID 0000-0002-7383-1484
Ada Maria TataDepartment of Biology and Biotechnologies, Sapienza University of Rome, Piazzale A. Moro 5, 00185 Rome, Italy.ORCID 0000-0003-4868-5435

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

α7 nAChRs are known to modulate several physiological and pathological functions in glial cells, and their selective activation might have anti-inflammatory effects in the central and peripheral nervous system. OL progenitors (OPCs) respond to cholinergic stimuli via muscarinic receptors that are mainly involved in the modulation of their proliferation. Conversely, the role of nicotinic receptors, particularly α7 nAChRs, has been poorly investigated. In this study, we evaluated the expression of α7 nAChRs in a model of OPCs (Oli neu) and the potential effects mediated by their selective activation.

methodsOli neu cells were used as a murine immortalized OPCs model. The effects of α7 nAChRs stimulation on cell proliferation and survival were assessed by the MTT assay. RT-PCR and Western blot analysis were used to analyze the expression of α7 nAChRs and proliferative and differentiative markers (PCNA, MBP). LPS exposure was used to induce the environment in which the antioxidant and anti-inflammatory properties of α7 nAChRs were analyzed, evaluating NFR2 and TNF-α expression, ROS levels through DCFDA staining while Oil Red O staining was used for the analysis of lipid droplet content as a marker of cellular inflammation response.

resultsThe α7 nAChR is expressed both in OPCs and OLs, and its stimulation by the selective agonist ICH3 increases cell proliferation without modifying the OLs' differentiation capability. Moreover, ICH3 showed anti-inflammatory and antioxidant effects against LPS exposure.

conclusionsThe results herein obtained confirm the role of α7 nAChR in the modulation of neuroinflammatory processes as well as their protective effects on OLs.

Indexed as

alpha7 Nicotinic Acetylcholine ReceptorNeuroinflammatory DiseasesOligodendrogliaAnimalsCell DifferentiationCell ProliferationCell SurvivalLipopolysaccharidesMiceReactive Oxygen Speciesalpha7 Nicotinic Acetylcholine ReceptorLipopolysaccharidesReactive Oxygen Speciescell proliferationneuroinflammationoligodendrocytesoxidative agentsα7 nicotinic receptors

Identifiers

PMID40643469
PMCPMC12248911

What Socratic holds

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LicenceCC BY
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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.