Effect of has-miR-150 on proliferation and apoptosis of Jurkat cells and its mechanism / 中国实验血液学杂志
Journal of Experimental Hematology
; (6): 94-98, 2015.
Artigo
em Chinês
| WPRIM (Pacífico Ocidental)
| ID: wpr-259634
Biblioteca responsável:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>This study was to investigate the effect of has-miR-150 on the proliferation and apoptosis in human acute T lymphocytic leukemia (T-ALL) cell line Jurkat, and explore its mechanism.</p><p><b>METHODS</b>Lentivirus-has-miR-150 was constructed and transfected to Jurkat cells. The expression of miR-150 was detected by real time PCR; the cell proliferation and apoptosis were detected by CCK-8 method and Annexin V/7-AAD labeling, respectively; the cell-related protein expressions of phosphatidylinositol-3-kinase(PI3K)/serine/ threonine kinase (Akt) signaling pathway were detected by Western blot.</p><p><b>RESULTS</b>The expression of miR-150 in infected Jurkat cells was significantly upregulated by constructing lentivirus-has-miR-150. Compared to negative control (transfected with empty-vector lentivirus), the cell proliferation after LV-miR-150 transfection was significantly inhibited and cell apoptosis was remarkably induced. Phosphorylation levels of P13K/Akt/NF-κB signaling pathway protein p-Akt and p-p65 decreased,whereas no obvious change was found in the expression of Akt.</p><p><b>CONCLUSION</b>miR-150 may be a putative oncoprotein in T-ALL cells. Overexpression of miR-150 has noticeable effects on the proliferation inhibition and apoptosis induction of Jurkat cells, which may be mediated by the negative regulation of PI3K/Akt /NF-κB signaling pathway.</p>
Texto completo:
Disponível
Base de dados:
WPRIM (Pacífico Ocidental)
Assunto principal:
Transfecção
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Transdução de Sinais
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Regulação para Cima
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NF-kappa B
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Apoptose
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Lentivirus
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Células Jurkat
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Fosfatidilinositol 3-Quinases
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MicroRNAs
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Proliferação de Células
Limite:
Humanos
Idioma:
Chinês
Revista:
Journal of Experimental Hematology
Ano de publicação:
2015
Tipo de documento:
Artigo