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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
1986-6-10
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pubmed:abstractText |
Using a mouse embryonal teratocarcinoma (E.C.) cell line, it was possible to follow the sequence of development of ionic channels during neuronal differentiation, with patch-clamp techniques. 1003 E.C. cells were induced to differentiate into neurons by culturing them in defined medium without foetal calf serum (DARMON et al., 1981). Non-differentiated cells were not excitable and presented mainly 2 types of K+ channels: a Ca2+ activated K+ channel (220 pS in symmetrical K+) and a delayed rectifier (30 pS in symmetrical K+). When the cells start to grow neurites, a low threshold calcium current can be recorded, only if the cell is held at hyperpolarized potentials (-70 to -80 mV). Fully differentiated cells with long neurites presented a complete repertoire of ionic channels: voltage dependent Na+ and Ca2+ channels, Ca2+ activated K+ channel and K+ delayed rectifier.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:issn |
0021-7948
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
80
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
312-20
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2422359-Animals,
pubmed-meshheading:2422359-Calcium,
pubmed-meshheading:2422359-Cell Differentiation,
pubmed-meshheading:2422359-Clone Cells,
pubmed-meshheading:2422359-Ion Channels,
pubmed-meshheading:2422359-Mice,
pubmed-meshheading:2422359-Neurons,
pubmed-meshheading:2422359-Phenotype,
pubmed-meshheading:2422359-Potassium,
pubmed-meshheading:2422359-Sodium,
pubmed-meshheading:2422359-Teratoma
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pubmed:year |
1985
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pubmed:articleTitle |
Development of ionic channels during mouse neuronal differentiation.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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