Long-term tripotent differentiation capacity of human neural stem (NS) cells in adherent culture

Yirui Sun, Steven Pollard, Luciano Conti, Mauro Toselli, Gerardo Biella, Georgina Parkin, Lionel Willatt, Anna Falk, Elena Cattaneo, Austin Smith

Research output: Contribution to journalArticlepeer-review

Abstract

Stem cell lines that provide a renewable and scaleable supply of central nervous system cell types would constitute an invaluable resource for basic and applied neurobiology. Here we describe the generation and long-term expansion of multiple human foetal neural stem (NS) cell lines in monolayer culture without genetic immortalization. Adherent human NS cells are propagated in the presence of epidermal growth factor (ELF) and fibroblast growth factor 2 (FGF2), under which conditions they stably express neural precursor markers and exhibit negligible differentiation into neurons or glia. However, they produce astrocytes, oligodendrocytes, and neurons upon exposure to appropriate differentiation factors. Single cell cloning demonstrates that human NS cells are tripotent. They retain a diploid karyotype and constant neurogenic capacity after over 100 generations. In contrast to human neurospheres, we observe no requirement for the cytokine leukaemia inhibitory factor (LIF) for continued expansion of adherent human NS cells. Human NS cells can be stably transfected to provide reporter lines and readily imaged in live monolayer cultures, creating the potential for high content genetic and chemical screens. (C) 2008 Elsevier Inc. All rights reserved.

Original languageEnglish
Pages (from-to)245-258
Number of pages14
JournalMolecular and Cellular Neuroscience
Volume38
Issue number2
DOIs
Publication statusPublished - Jun 2008

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