Stem Cell Research & Therapy · 2013 · 27 citations · 30 references
Life SciencesCell BiologyNeuroscienceCellular NeuroscienceDevelopmental NeuroscienceStem Cell BiologyNeural DevelopmentNeural Stem Cell BiologyNeural Stem CellsNeurogenesisNeuronal DevelopmentNeuronal DifferentiationNeural Stem Cell MarkersNeural Stem Cell TransplantationNeurogenic DifferentiationNeuronal Fate DeterminationProgenitor CellsSpinal Cord LesionsSpinal Cord TissueStem Cell-derived Cell Lines
INTRODUCTION: The use of immortalized neural stem cells either as models of neural development in vitro or as cellular therapies in central nervous system (CNS) disorders has been controversial. This controversy has centered on the capacity of immortalized cells to retain characteristic features of the progenitor cells resident in the tissue of origin from which they were derived, and the potential for tumorogenicity as a result of immortalization. Here, we report the generation of conditionally immortalized neural stem cell lines from human fetal spinal cord tissue, which addresses these issues. METHODS: Clonal neural stem cell lines were derived from 10-week-old human fetal spinal cord and conditionally immortalized with an inducible form of cMyc. The derived lines were karyotyped, transcriptionally profiled by microarray, and assessed against a panel of spinal cord progenitor markers with immunocytochemistry. In addition, the lines were differentiated and assessed for the presence of neuronal fate markers and functional calcium channels. Finally, a clonal line expressing eGFP was grafted into lesioned rat spinal cord and assessed for survival, differentiation characteristics, and tumorogenicity. RESULTS: We demonstrate that these clonal lines (a) retain a clear transcriptional signature of ventral spinal cord progenitors and a normal karyotype after extensive propagation in vitro, (b) differentiate into relevant ventral neuronal subtypes with functional T-, L-, N-, and P/Q-type Ca(2+) channels and spontaneous calcium oscillations, and (c) stably engraft into lesioned rat spinal cord without tumorogenicity. CONCLUSIONS: We propose that these cells represent a useful tool both for the in vitro study of differentiation into ventral spinal cord neuronal subtypes, and for examining the potential of conditionally immortalized neural stem cells to facilitate functional recovery after spinal cord injury or disease.
30
Pax6 Controls Progenitor Cell Identity and Neuronal Fate in Response to Graded Shh Signaling
Johan Ericson, Penny Rashbass, Andreas Schedl et al. · Cell · 1997 · 1.1K citations · Full text
Regulation of growth cone behavior by calcium
SB Kater, LR Mills · Journal of Neuroscience · 1991 · 594 citations · Full text