Abstract
An intracellular timer is thought to help control the timing of oligodendrocyte differentiation. We show here that the expression of the helix-loop-helix gene Id4 in oligodendrocyte precursor cells decreases in vivo and in vitro with a time course expected if Id4 is part of the timer. We also show that Id4 expression decreases prematurely when the precursor cells are induced to differentiate by mitogen withdrawal. Both Id4 mRNA and protein decrease together under all of these conditions, suggesting that the control of Id4 expression is transcriptional. Finally, we show that enforced expression of Id4 stimulates cell proliferation and blocks differentiation induced by either mitogen withdrawal or treatment with thyroid hormone. These findings suggest that a progressive fall in Id4 transcription is part of the intracellular timer that helps determine when oligodendrocyte precursor cells withdraw from the cell cycle and differentiate.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Biological Clocks / genetics
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Biological Clocks / physiology
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Cell Differentiation* / drug effects
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Cell Division / drug effects
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Cells, Cultured
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DNA-Binding Proteins*
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Fluorescent Antibody Technique
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Gene Expression
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Helix-Loop-Helix Motifs*
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Inhibitor of Differentiation Protein 1
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Inhibitor of Differentiation Proteins
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Kinetics
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Mitogens / deficiency
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Mitogens / pharmacology
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Oligodendroglia / cytology*
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Oligodendroglia / drug effects
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Oligodendroglia / metabolism
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Platelet-Derived Growth Factor / deficiency
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Platelet-Derived Growth Factor / pharmacology
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Proteins / chemistry*
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Proteins / genetics
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Proteins / metabolism*
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RNA, Messenger / genetics
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RNA, Messenger / metabolism
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Rats
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Rats, Sprague-Dawley
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Repressor Proteins*
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Stem Cells / cytology
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Stem Cells / drug effects
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Stem Cells / metabolism
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Temperature
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Thyroid Hormones / pharmacology
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Time Factors
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Transcription Factors / genetics
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Transcription Factors / metabolism
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Transfection
Substances
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DNA-Binding Proteins
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ID1 protein, rat
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Id4 protein, rat
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Inhibitor of Differentiation Protein 1
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Inhibitor of Differentiation Proteins
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Mitogens
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Platelet-Derived Growth Factor
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Proteins
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RNA, Messenger
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Repressor Proteins
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Thyroid Hormones
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Transcription Factors