A crucial role for p57(Kip2) in the intracellular timer that controls oligodendrocyte differentiation

Authors:
Dugas JC, Ibrahim A, Barres BA
In:
Source: J Neurosci
Publication Date: (2007)
Issue: 27(23): 6185-96
Research Area:
Neurobiology
Cells used in publication:
Oligodendrocyte, rat
Species: rat
Tissue Origin: brain
Platform:
Nucleofector® I/II/2b
Experiment
Rat Oligodendrocyte Nucleofector Kit was used in combination with program O-017. 2-3 million cells and 1.5-4 µg plasmid DNA was used per reaction. 100-200 pmol siGenome SMARTPool from Dharmacon directed against different targets was used.
Abstract
The intracellular molecular mechanism that controls the timing of oligodendrocyte differentiation remains unknown. Temple and Raff (1986) previously showed that an oligodendrocyte precursor cell (OPC) can divide a maximum of approximately eight times before its daughter cells simultaneously cease proliferating and differentiate into oligodendrocytes. They postulated that over time the level of an intracellular molecule might synchronously change in each daughter cell, ultimately reaching a level that prohibited additional proliferation. Here, we report the discovery of such a molecule, the cyclin-dependent kinase inhibitor p57(Kip2) (Cdkn1c). We show in vitro that all daughters of a clone of OPCs express similar levels of p57(Kip2), that p57(Kip2) levels increase over time in proliferating OPCs, and that p57(Kip2) levels regulate how many times an OPC can divide before differentiating. These findings reveal a novel part of the mechanism by which OPCs measure time and are likely to extend to similar timers in many other precursor cell types.