Abstract
Commercially available microcarriers (MCs), which are briefly described here, are usually used as a support for culturing a variety of cells both on laboratory and on an industrial scale. Selected MCs are used as a culture system for embryonic dissociated CNS cells and myoblasts. The tridimensional support provided by the MCs, enables neuronal and muscle cells to grow and differentiate into functional cell-MC units, which remain floating in the culture medium. The neuronal entities are characterized by intensive fiber growth followed by synaptogenesis and myelination. The muscular units develop striated myotubes, having the same orientation, which contract spontaneously. The MC technique is advantageous over the conventional monolayer procedure, allowing cells to grow to higher amounts at a better efficiency for longer periods. Functional units can be sampled without interfering with the ongoing culture. We consider the use of these cultures, as well as nerve muscle MC co-cultures as a tool for the study of neurotoxicology. The possibility of implantation of such functional culture units into injured adult nerve and muscle tissues is being considered.
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Abbreviations
- AChE:
-
Acetylcholinesterase
- CNS:
-
Central nervous system
- DIV:
-
Days in vitro
- MC:
-
Microcarrier
- MCs:
-
Microcarriers
- SEM:
-
Scanning electron microscope or micrographs
- TEM:
-
Transmission electron microscope or micrographs
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© 1987 Springer-Verlag
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Shahar, A., Reuveny, S. (1987). Nerve and muscle cells on microcarriers in culture. In: Vertrebrate Cell Culture I. Advances in Biochemical Engineering/Biotechnology, vol 34. Springer, Berlin, Heidelberg. https://doi.org/10.1007/BFb0000672
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DOI: https://doi.org/10.1007/BFb0000672
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