CG-4, A new bipotential glial cell line from rat brain, is capable of differentiating in vitro into either mature oligodendrocytes or type-2 astrocytes
Autor: | S. Varon, Ella Magal, Jean-Claude Louis, David Muir, Marston Manthorpe |
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Rok vydání: | 1992 |
Předmět: |
Swine
Cellular differentiation Biology Cell Line Neuroblastoma Cellular and Molecular Neuroscience Tumor Cells Cultured medicine Animals Humans Progenitor cell Growth Substances Cerebral Cortex Cell Differentiation Rats Inbred Strains Oligodendrocyte Culture Media Rats Cell biology Oligodendroglia Phenotype medicine.anatomical_structure P19 cell Animals Newborn Cell culture Astrocytes Karyotyping Immunology Neuroglia Galactocerebroside Cell Division Astrocyte |
Zdroj: | Journal of Neuroscience Research. 31:193-204 |
ISSN: | 1097-4547 0360-4012 |
Popis: | We have established a permanent cell line (CG-4) of rat central nervous system glial precursors from primary cultures of bipotential oligodendrocyte-type 2-astrocyte (O-2A) progenitor cells, which were kept proliferating with the mitogen(s) secreted by the neuronal B104 cell line. The CG-4 cells have a normal karyotype and display the properties of normal O-2A cells. CG-4 cells can be propagated in serum-free culture medium supplemented with medium conditioned by B104 cells for unrestricted periods of time as O-2A cells, characterized by the presence of the A2B5 surface marker and the absence of markers specific for oligodendrocytes (galactocerebroside, myelin basic protein) or type 2-astrocytes (glial acidic fibrillary protein). bFGF and PDGF are potent mitogens for CG-4 cells and their combination can substitute for the B104-derived mitogen(s). CG-4 cells are capable of differentiating into either oligodendrocytes or type 2-astrocytes. Differentiation into oligodendrocytes occurs after withdrawal of the mitogen. Replacement of the mitogen with fetal calf serum (20%), in contrast, induces 50% of the CG-4 cells to differentiate into type 2-astrocytes. Pure cultures of oligodendrocytes or type 2-astrocytes can be generated in substantial amounts from CG-4 cells and maintained for several weeks in medium containing 5% fetal calf serum. |
Databáze: | OpenAIRE |
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