Background: There is an urgent need of neuronal cell models to be applied to high-throughput screening settings while recapitulating physiological and/or pathological events occurring in the Central Nervous System (CNS). Stem cells offer a great opportunity in this direction since their self renewal capacity allows for large scale expansion. Protocols for directed differentiation also promise to generate populations of biochemically homogenous neuronal progenies. NS (Neural Stem) cells are a novel population of stem cells that undergo symmetric cell division in monolayer and chemically defined media, while remaining highly neurogenic.Results: We report the full adaptation of the NS cell systems for their growth and neuronal differentiation to 96- and 384-well microplates. This optimized system has also been exploited in homogeneous and high-content assays.Conclusions: Our results show that these mouse NS cells may be suitable for a series of applications in high-throughput format. © 2010 Garavaglia et al; licensee BioMed Central Ltd.

Adaptation of NS cells growth and differentiation to high-throughput screening-compatible plates

BOLOGNINI, DANIELE;Papait, Roberto;
2010-01-01

Abstract

Background: There is an urgent need of neuronal cell models to be applied to high-throughput screening settings while recapitulating physiological and/or pathological events occurring in the Central Nervous System (CNS). Stem cells offer a great opportunity in this direction since their self renewal capacity allows for large scale expansion. Protocols for directed differentiation also promise to generate populations of biochemically homogenous neuronal progenies. NS (Neural Stem) cells are a novel population of stem cells that undergo symmetric cell division in monolayer and chemically defined media, while remaining highly neurogenic.Results: We report the full adaptation of the NS cell systems for their growth and neuronal differentiation to 96- and 384-well microplates. This optimized system has also been exploited in homogeneous and high-content assays.Conclusions: Our results show that these mouse NS cells may be suitable for a series of applications in high-throughput format. © 2010 Garavaglia et al; licensee BioMed Central Ltd.
2010
Adult Stem Cells; Animals; Apoptosis; Cell Culture Techniques; Cell Differentiation; Cell Line; Cell Survival; Cyclic AMP; High-Throughput Screening Assays; Mice; Mice, Inbred Strains; Neurogenesis; Neurons; Oxidative Stress; Receptors, GABA-A; Stem Cell Niche; Time Factors; Neuroscience (all); Cellular and Molecular Neuroscience
Garavaglia, Alessia; Moiana, Alessia; Camnasio, Stefano; Bolognini, Daniele; Papait, Roberto; Rigamonti, Dorotea; Cattaneo, Elena
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11383/2072366
 Attenzione

L'Ateneo sottopone a validazione solo i file PDF allegati

Citazioni
  • ???jsp.display-item.citation.pmc??? 3
  • Scopus 10
  • ???jsp.display-item.citation.isi??? 9
social impact