Evidence map›Paper›PMID 41890905›Full record

ArticleFrontiers in cell and developmental biology2026

A conserved bioelectrical signature defines subventricular zone-derived human fetal neural stem cells and tracks their differentiation state.

Roberta De Zio, Diletta Lucia Capobianco, Daniela Celeste Profico, Giada D'Aloisio, Giuseppe Procino, Maurizio Gelati, Angelo Luigi Vescovi, Francesco Pisani, Maria Svelto, Andrea Gerbino

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Article in Frontiers in cell and developmental biology, 2026. 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

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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

1 citing paper in PubMed.

  1. Absolute voltage mapping using dynamic photocycle control.bioRxiv : the preprint server for biology · 2026
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4 · The record

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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.

Roberta De ZioDepartment of Biosciences, Biotechnologies and Environment, University of Bari "Aldo Moro", Bari, Italy.
Diletta Lucia CapobiancoDepartment of Biosciences, Biotechnologies and Environment, University of Bari "Aldo Moro", Bari, Italy.
Daniela Celeste ProficoProPharma LLC, Leiden, Netherlands.
Giada D'AloisioIRCSS Casa Sollievo della Sofferenza, Unità Produttiva per Terapie Avanzate, San Giovanni Rotondo, Italy.
Giuseppe ProcinoDepartment of Biosciences, Biotechnologies and Environment, University of Bari "Aldo Moro", Bari, Italy.
Maurizio GelatiFondazione IRCSS Istituto Neurologico "C.Besta", Milan, Italy.
Angelo Luigi VescoviFaculty of Medicine, Link Campus University, Rome, Italy.
Francesco PisaniDepartment of Biosciences, Biotechnologies and Environment, University of Bari "Aldo Moro", Bari, Italy.
Maria SveltoDepartment of Biosciences, Biotechnologies and Environment, University of Bari "Aldo Moro", Bari, Italy.
Andrea GerbinoDepartment of Biosciences, Biotechnologies and Environment, University of Bari "Aldo Moro", Bari, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Human fetal neural stem cells (hfNSCs) from the subventricular zone (SVZ) are employed in clinical trials for neurodegenerative diseases, yet their bioelectrical properties remain largely unexplored. Molecular markers alone do not reliably correlate with functional state, highlighting the need for complementary functional descriptors. Methods: We performed whole-cell patch-clamp recordings on hfNSCs from three independent SVZ donors (15-16 weeks of gestation) to characterize resting membrane potential (Vm) and voltage-gated currents, assessing inter-donor reproducibility and differentiation dynamics over 30 days Results: hfNSCs exhibited a highly reproducible bioelectrical signature across all donors, characterized by a depolarized resting membrane potential (∼-30 mV), a non-excitable profile, and a stereotyped composition of outward K+ currents. The two current components were resolved using combined biophysical and pharmacological approaches, while Western blot analysis confirmed the expression of Kv4.2 and Kv1.1 channel subtypes functionally consistent with I Conclusion: SVZ-derived hfNSCs possess a reproducible bioelectrical signature within the 15-16-week gestational window across independent donors, supporting electrophysiological profiling as a quantitative functional benchmark for identity and standardization. During

Indexed as

ion channelK+ currentsresting membrane potentialstem cellstemness marker

Identifiers

PMID41890905
PMCPMC13014620

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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.