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Jeruzalska, E.* ; Ketteler, C. ; Stützenberger, E.* ; Burczyk, S.* ; Möller, L.* ; Niessing, D.

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

Biochem. Biophys. Rep. 46:102655 (2026)
Verlagsversion Forschungsdaten DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
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.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Astrocytes ; Hns1 ; Human Neural Stem Cells ; Immortalized Cell Line ; Neurodegeneration ; Neurodevelopment ; Neurons ; Oligodendrocytes
ISSN (print) / ISBN 2405-5808
e-ISSN 2405-5808
Quellenangaben Band: 46, Heft: , Seiten: , Artikelnummer: 102655 Supplement: ,
Verlag Elsevier
Begutachtungsstatus Peer reviewed