Cell cycle control of Schwann cell proliferation: Role of cyclin-dependent kinase-2

被引:39
|
作者
Tikoo, R
Zanazzi, G
Shiffman, D
Salzer, J
Chao, MV
机构
[1] NYU, Sch Med, Skirball Inst Biomol Med, New York, NY 10016 USA
[2] NYU, Sch Med, Dept Cell Biol, New York, NY 10016 USA
[3] Cornell Univ, Weill Med Coll, Dept Neurol & Neurosurg, New York, NY 10021 USA
来源
JOURNAL OF NEUROSCIENCE | 2000年 / 20卷 / 12期
关键词
Schwann cell; proliferation; growth arrest; cyclin-dependent kinase; cell cycle; DRG;
D O I
10.1523/JNEUROSCI.20-12-04627.2000
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Schwann cell proliferation is regulated by multiple growth factors and axonal signals. However, the molecules that control growth arrest of Schwann cells are not well defined. Here we describe regulation of the cyclin-dependent kinase-2 (CDK2) protein, an enzyme that is necessary for the transition from G1 to S phase. Levels of CDK2 protein were elevated in proliferating Schwann cells cultured in serum and forskolin. However, when cells were grown with either serum-free media or at high densities, CDK2 levels declined to low levels. The decrease in CDK2 levels was associated with growth arrest of Schwann cells. The modulation of CDK2 appears to be regulated at the transcriptional level, because CDK2 mRNA levels and its promoter activity both decline during cell cycle arrest. Furthermore, analysis of the CDK2 promoter suggests that Sp1 DNA binding sites are essential for maximal activation in Schwann cells. Together, these data suggest that CDK2 may represent a significant target of developmental signals that regulate Schwann cell proliferation and that this regulation is mediated, in part, through regulation of Sp1 transcriptional activity.
引用
收藏
页码:4627 / 4634
页数:8
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