Evidence map›Paper›PMID 42256314›Full record

ArticleFrontiers in molecular biosciences2026

NMR metabolomics assessment of neural commitment of human dental pulp-derived stem cells.

Mattea Chirico, Maria Elena Pisanu, Emanuela Mari, Valeria Manganelli, Fanny Pulcini, Loreto Lancia, Rita Di Benedetto, Simona Delle Monache, Egidio Iorio, Vincenzo Mattei

Abstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

10 authors.

Mattea Chirico *High Resolution NMR Unit, Core Facilities, Istituto Superiore di Sanità, Roma, Italy.
Maria Elena Pisanu *High Resolution NMR Unit, Core Facilities, Istituto Superiore di Sanità, Roma, Italy.
Emanuela MariDepartment of Life Science, Health and Health Professions, Link Campus University, Roma, Italy.
Valeria ManganelliDepartment of Experimental Medicine, "Sapienza" University of Roma, Roma, Italy.
Fanny PulciniDepartment of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
Loreto LanciaDepartment of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
Rita Di BenedettoDepartment of Food Safety, Nutrition and Veterinary Public Health, Istituto Superiore di Sanità, Roma, Italy.
Simona Delle MonacheDepartment of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
Egidio Iorio *High Resolution NMR Unit, Core Facilities, Istituto Superiore di Sanità, Roma, Italy.
Vincenzo Mattei *Department of Life Science, Health and Health Professions, Link Campus University, Roma, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Mesenchymal stem cells, particularly those derived from dental pulp cells (DPSCs), hold promising potential for neuro-regenerative therapies due to their multipotency and accessibility. Neural differentiation is closely linked to cellular metabolic reprogramming, yet the specific metabolic shifts alterations involved in DPSC neurogenesis remain underexplored. Methods: Neural commitment was induced by 14 days of differentiation with EGF and bFGF. Untargeted proton nuclear magnetic resonance ( Results: Following 14 days of differentiation with EGF and bFGF, DPSCs exhibited a marked decrease in mesenchymal markers (CD44, CD90, CD105) and an increase in neural markers (β3-tubulin, NFH), alongside morphological changes toward a neuron-like phenotype. Metabolomics analysis revealed changes in metabolite levels, including increased aspartic acid and phosphocholine and reduced alanine, glutamate, and myo-inositol. Exploratory lipid analyses, suggested increased fatty acid and triacylglycerol content together with a higher PUFA/MUFA ratio. Pathway enrichment analyses highlighted amino acid metabolism and phosphoinositide signaling as potentially relevant. Understanding these changes enhances our knowledge of stem cell differentiation and supports the therapeutic potential of DPSCs in neuro-regenerative medicine. Conclusion: These findings provide a descriptive metabolic characterization of DPSC neural commitment and identify candidate metabolite changes associated with early neural differentiation. While the results support the occurrence of metabolic remodelling during neural induction, further studies integrating functional and flux-based approaches are required to define the biological significance of these alterations.

Indexed as

1H NMRamino acid metabolismdental pulp stem cellsmetabolomicsneural commitment

Identifiers

PMID42256314
PMCPMC13236527

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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.