Back to Search
Start Over
Bipotent progenitor cell lines from the human CNS
- Source :
- Nature Biotechnology. 15:574-580
- Publication Year :
- 1997
- Publisher :
- Springer Science and Business Media LLC, 1997.
-
Abstract
- Human central nervous system (CNS) cell lines would substantially facilitate drug discovery and basic research by providing a readily renewable source of human neurons. We isolated clonal human CNS cell lines that had been immortalized with a tetracycline (Tc)-responsive v-myc oncogene; addition of Tc to the growth medium suppressed the oncoprotein rapidly and virtually completely, allowing differentiation to proceed. Two classes of bipotent precursor cells were immortalized: the first class had a default differentiation pathway of neurons only, and the second class had a default differentiation pathway of neurons and astrocytes. We found that after exposure to different external signals in vitro, the environment is capable of redirecting the fate of a particular cell, even in the case of the bipotent precursor cell whose default differentiation pathway was neurons only. These data suggest that extrinsic cues can prevail over intrinsic determinants in directing cell fate in the human CNS.
- Subjects :
- Oncogene Protein p55(v-myc)
N-Methylaspartate
Cellular differentiation
Models, Neurological
Cell
Cell Culture Techniques
Genes, myc
Glycine
Biomedical Engineering
Gestational Age
Bioengineering
Cell fate determination
Biology
Transfection
Applied Microbiology and Biotechnology
Cell Line
Membrane Potentials
Fetus
Precursor cell
medicine
Humans
Progenitor cell
gamma-Aminobutyric Acid
Cell Line, Transformed
Neurons
Kainic Acid
Brain-Derived Neurotrophic Factor
Stem Cells
Brain
Cell Differentiation
Recombinant Proteins
Cell biology
medicine.anatomical_structure
Bucladesine
Cell culture
Astrocytes
Immunology
Molecular Medicine
Neuron
Biotechnology
Subjects
Details
- ISSN :
- 15461696 and 10870156
- Volume :
- 15
- Database :
- OpenAIRE
- Journal :
- Nature Biotechnology
- Accession number :
- edsair.doi.dedup.....cc386e8adcec373ac811a4aa617002d8
- Full Text :
- https://doi.org/10.1038/nbt0697-574