OSCR

Comprehensive characterization of the human neural stem cell line HNSC.100 as a versatile model for neurobiological research.

Overview

Authors: Estera Jeruzalska1, Carolin Ketteler2, Elisa Stützenberger1, Sandra Burczyk1, Larissa Möller1, Dierk Niessing1,2
ORCID iDs: Dierk Niessing
  1. Institute of Pharmaceutical Biotechnology, Ulm University, James-Franck-Ring N27, Ulm, 89081, Germany
  2. Molecular Targets and Therapeutics Center, Institute of Structural Biology, Helmholtz Zentrum München, German Research Center for Environmental Health, Ingolstädter Landstr. 1, Neuherberg, 85764, Germany
Institutions: Universität Ulm (Germany); Helmholtz Munich (Germany)
Journal: Biochemistry and biophysics reports, volume 46, article 102655
Dates: received 8 January 2026; accepted 27 May 2026; published online 2 June 2026
Type: Brief report · Language: English
License: CC BY
Identifiers: DOI 10.1016/j.bbrep.2026.102655 · PMID 42282851 · PMCID PMC13251743 · OpenAlex W7163189724
Open access: gold, a free copy (OpenAlex)
Status: data only
Categories: human (organism)
Methods: Statistics, Evoked potentials
Keywords: Human neural stem cells, Immortalized cell line, Neurodegeneration, Neurodevelopment, Astrocytes, Neurons, Oligodendrocytes, hNS1
Topic: Neurogenesis and neuroplasticity mechanisms (Developmental Neuroscience, Neuroscience), according to OpenAlex
Funding: Deutsche Forschungsgemeinschaft (541627224, NI 2094/11-1)
Citations: not cited yet (Europe PMC); 37 references in the paper

Abstract

Studying neural-related questions is inherently challenging due to the limited number of suitable cell models. Here, we characterize a previously reported immortalized human neural stem cell line, HNSC.100, serving as a robust model for a wide range of neurobiological research questions. The cell line expresses key neural stem cell markers, including SOX2, vimentin, nestin, and allows for efficient genetic manipulation. Furthermore, HNSC.100 cells can be differentiated into neurons, astrocytes, and oligodendrocytes, thereby covering a wide spectrum of major neural cell types. We adapted corresponding differentiation protocols and established a comprehensive panel of molecular markers to validate successful differentiation, enabling precise characterization of the resulting cell population. In addition, we provide a complete dataset of RNA expression levels for all detectable genes in HNSC.100 cells. Based on this dataset, we assembled a list of expressed genes implicated in neural disorders that can be studied with this cell line. Together, we present a detailed characterization of the HNSC.100 cell line and provide new tools and reference data to facilitate its use. This resource enables researchers to evaluate the line's suitability for specific applications and to rapidly integrate HNSC.100 cells into their experimental workflows.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

The paper links to its data, not to its authors' code: see the Data section.

Tracing map

A tracing map links a paper to the code its authors published: this paper has none, so it has no map.

Data

Datasets cited

Data availability

Data will be made available on request.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 2, 28 September 2026

  • Authors: added Dierk Niessing (0000-0002-5589-369X); removed Dierk Niessing

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, pages, dates, 6 authors, 8 keywords, 1 funder, 36 references.

Cite

This paper

Jeruzalska, E., Ketteler, C., Stützenberger, E., Burczyk, S., Möller, L., & Niessing, D. (2026). Comprehensive characterization of the human neural stem cell line HNSC.100 as a versatile model for neurobiological research. Biochemistry and biophysics reports, 46, 102655. https://doi.org/10.1016/j.bbrep.2026.102655

BibTeX

@article{jeruzalska2026comprehensive,
author = {Jeruzalska, Estera and Ketteler, Carolin and Stützenberger, Elisa and Burczyk, Sandra and Möller, Larissa and Niessing, Dierk},
title = {{Comprehensive characterization of the human neural stem cell line HNSC.100 as a versatile model for neurobiological research}},
journal = {Biochemistry and biophysics reports},
year = {2026},
month = jun,
volume = {46},
pages = {102655},
publisher = {Elsevier},
issn = {2405-5808},
doi = {10.1016/j.bbrep.2026.102655},
url = {https://doi.org/10.1016/j.bbrep.2026.102655},
pmid = {42282851},
pmcid = {PMC13251743}
}

RIS

TY - JOUR
AU - Jeruzalska, Estera
AU - Ketteler, Carolin
AU - Stützenberger, Elisa
AU - Burczyk, Sandra
AU - Möller, Larissa
AU - Niessing, Dierk
TI - Comprehensive characterization of the human neural stem cell line HNSC.100 as a versatile model for neurobiological research
T2 - Biochemistry and biophysics reports
J2 - Biochem Biophys Rep
PY - 2026
DA - 2026/06/02
VL - 46
SP - 102655
SN - 2405-5808
PB - Elsevier
DO - 10.1016/j.bbrep.2026.102655
UR - https://doi.org/10.1016/j.bbrep.2026.102655
LA - en
ER -

CSL-JSON

{
"id": "10.1016/j.bbrep.2026.102655",
"type": "article-journal",
"title": "Comprehensive characterization of the human neural stem cell line HNSC.100 as a versatile model for neurobiological research",
"container-title": "Biochemistry and biophysics reports",
"author": [
{
"family": "Jeruzalska",
"given": "Estera"
},
{
"family": "Ketteler",
"given": "Carolin"
},
{
"family": "Stützenberger",
"given": "Elisa"
},
{
"family": "Burczyk",
"given": "Sandra"
},
{
"family": "Möller",
"given": "Larissa"
},
{
"family": "Niessing",
"given": "Dierk"
}
],
"container-title-short": "Biochem Biophys Rep",
"volume": "46",
"page": "102655",
"DOI": "10.1016/j.bbrep.2026.102655",
"PMID": "42282851",
"PMCID": "PMC13251743",
"ISSN": "2405-5808",
"publisher": "Elsevier",
"URL": "https://doi.org/10.1016/j.bbrep.2026.102655",
"language": "en",
"issued": {
"date-parts": [
[
2026,
6,
2
]
]
}
}

Similar papers

The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.

[1] doi:10.1038/s41420-026-02971-w [code]
Multi-omics reveals heterogeneity and functional populations of oligodendrocyte progenitor cells induced by human neural stem cells.
Journal: Cell death discovery
In common: 3 references
[2] doi:10.3390/bioengineering13050500
SOX10 Overexpression Enhances the Oligodendrocyte Lineage Commitment of iOPCs In Vitro by Reshaping Their Chromatin Binding Landscape.
Journal: Bioengineering (Basel, Switzerland)
In common: 2 references
[3] doi:10.1126/sciadv.aed8653
Targeting astrocytic Dp71 attenuates BBB disruption after traumatic brain injury through WTAP-associated m<sup>6</sup>A regulation of MMP2.
Journal: Science advances
In common: 2 references
[4] doi:10.1038/s41398-026-04142-y [code]
Phocaeicola vulgatus improves anxiety-like behavior by ameliorating amygdala neuroinflammation and the neurite impairment in IBS.
Journal: Translational psychiatry
In common: 1 reference
[5] doi:10.1038/s41467-026-74058-0
IQGAP3 bridges matrix stiffness with glioma stem cell maintenance and radioresistance by stabilizing SOX2.
Journal: Nature communications
In common: 1 reference
[6] doi:10.3389/fnagi.2026.1761218
Integrated transcriptomic profiling combined with <i>in vitro</i> validation reveals the involvement of TMEM140 in the link between periodontitis and brain aging.
Journal: Frontiers in aging neuroscience
In common: 1 reference
[7] doi:10.1016/j.isci.2026.117028
Intermittent fasting promotes remodeling of neural and vascular networks in visceral white adipose tissue.
Journal: iScience
In common: 1 reference
[8] doi:10.1016/j.stemcr.2026.103020
Brain corticogenesis promotes SARS-CoV-2 neuro-glial tropism through lipid-dependent viral replication.
Journal: Stem cell reports
In common: 1 reference
[9] doi:10.1158/0008-5472.can-25-2237 [code]
Extracellular Vesicle-Mediated O-GlcNAcase Transfer Drives Neuronal Necroptosis to Facilitate Gallbladder Cancer Perineural Invasion.
Journal: Cancer research
In common: 1 reference
[10] doi:10.1093/neuonc/noag059
Combined patch-clamp electrophysiology and single-cell genomic analysis reveal spiking tumor cells at the neocortical glioblastoma interface in humans.
Journal: Neuro-oncology
In common: 1 reference

Contribute

The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.

Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.

Request its removal

To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).

Discussion, reproductions, activity

Discussion: questions and error reports about this paper and its code, from signed-in readers and its authors. It opens with sign-in.

Reproductions: reports from readers who ran the authors' code: what they reproduced, with which environment, commit and data. It opens with sign-in.

Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.