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Expression variation and significance of Skp2 and p27(kip1) during the proliferation of Jurkat cells / 中华肿瘤杂志
Chinese Journal of Oncology ; (12): 330-334, 2008.
Article Dans Chinois | WPRIM | ID: wpr-348100
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the expression variation and significance of Skp2 and p27(kip1) during the proliferation of lymphoma cell line Jurkat cells.</p><p><b>METHODS</b>The binding of p27(kip1) and Skp2 in Jurkat cells were detected by immunoprecipitation. Jurkat cells were treated with serum starvation and release synchronization. The expression variation and subcellular localization of p27(kip1) and Skp2 were detected by subcellular fractionation, Western blot and double immunofluorescence labelling.</p><p><b>RESULTS</b>The results of immunoprecipitation suggested that p27(kip1) and Skp2 could bind each other in Jurkat cells. During the proliferation of Jurkat cells, the protein expression of p27(kip1) decreased and intranuclear p27(kip1) decreased significantly, while the Skp2 protein increased and cytoplasmic Skp2 increased significantly.</p><p><b>CONCLUSION</b>During the proliferation of Jurkat cells, the increased cytoplasmic synthesis of Skp2 may speed up p27(kip1) degradation via the ubiquitin-proteasome pathway, then intranuclear p27(kip1) decreases significantly, leading to an increased cell cycling activity.</p>
Sujets)
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Anatomopathologie / Liaison aux protéines / Noyau de la cellule / Lymphome B / Cellules Jurkat / Cytoplasme / Protéines associées aux kinases de la phase S / Prolifération cellulaire / Inhibiteur p27 de kinase cycline-dépendante / Métabolisme Limites du sujet: Humains langue: Chinois Texte intégral: Chinese Journal of Oncology Année: 2008 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Anatomopathologie / Liaison aux protéines / Noyau de la cellule / Lymphome B / Cellules Jurkat / Cytoplasme / Protéines associées aux kinases de la phase S / Prolifération cellulaire / Inhibiteur p27 de kinase cycline-dépendante / Métabolisme Limites du sujet: Humains langue: Chinois Texte intégral: Chinese Journal of Oncology Année: 2008 Type: Article