Myelination in rat brain aggregating cell cultures.

Details

Serval ID
serval:BIB_AD790D9F55CA
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Myelination in rat brain aggregating cell cultures.
Journal
Neuroscience
Author(s)
Matthieu J.M., Honegger P., Trapp B.D., Cohen S.R., Webster H.F.
ISSN
0306-4522 (Print)
ISSN-L
0306-4522
Publication state
Published
Issued date
1978
Volume
3
Number
6
Pages
565-572
Language
english
Abstract
Aggregates of fetal rat brain were maintained in rotating culture for 30-40 days and were analyzed morphologically and biochemically. At 4 days in culture all cells were undifferentiated. At 26 days in vitro over 90% of all cells within the aggregates could be identified as neurons, astrocytes or oligodendrocytes. Myelinated axons and morphologically mature synapses were present at 26 days. Myelination started between 18 and 19 days in culture as determined biochemically. Myelin basic protein sulphatide synthesis and 2′,3′-cyclic nucleotide 3′-phosphohydrolase activity increased with in vitro age. The amount of myelin observed within the aggregates was much lower than observed at the corresponding age in vivo. Neurons and neuronal processes were undergoing severe degeneration in the 40-day aggregates and synaptic contacts were not maintained. There were no normal myelinated axons at 40 days although multilammellar membranes were found intra- and extracellularly. The ganglioside pattern of the aggregates were qualitatively similar to rat whole brain. Quantitatively the GM3ganglioside was elevated in comparison to whole rat brain.
Our results indicate that aggregating rat brain cultures provide a useful in vitro system for the biochemical and morphological analysis of myelin formation.
Keywords
2',3'-Cyclic-Nucleotide Phosphodiesterases/analysis, Animals, Brain/embryology, Brain Chemistry, Cells, Cultured, Lipids/analysis, Myelin Proteins/analysis, Myelin Sheath, Nerve Tissue Proteins/analysis, Rats
Pubmed
Web of science
Create date
24/01/2008 14:11
Last modification date
20/08/2019 16:17
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