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Cell cycle control of Schwann cell proliferation: role of cyclin-dependent kinase-2.
Tikoo, R; Zanazzi, G; Shiffman, D; Salzer, J; Chao, M V.
Afiliación
  • Tikoo R; Department of Neurology and Neuroscience, Weill Medical College of Cornell University, New York, New York 10021, USA.
J Neurosci ; 20(12): 4627-34, 2000 Jun 15.
Article en En | MEDLINE | ID: mdl-10844032
ABSTRACT
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.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Células de Schwann / Ciclo Celular / Proteínas Proto-Oncogénicas / Proteínas Serina-Treonina Quinasas / Quinasas Ciclina-Dependientes / Quinasas CDC2-CDC28 / Neuronas Idioma: En Revista: J Neurosci Año: 2000 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Células de Schwann / Ciclo Celular / Proteínas Proto-Oncogénicas / Proteínas Serina-Treonina Quinasas / Quinasas Ciclina-Dependientes / Quinasas CDC2-CDC28 / Neuronas Idioma: En Revista: J Neurosci Año: 2000 Tipo del documento: Article