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Effects and Mechanism of PARP Inhibitor Olaparib on the Expression of NKG2D Ligands in HL-60 Cells / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 1826-1830, 2020.
Article em Zh | WPRIM | ID: wpr-879978
Biblioteca responsável: WPRO
ABSTRACT
OBJECTIVE@#To investigate the regulatory effects of Olaparib on natural killer cell activating receptor (NKG2D) ligands expression on human acute myeloid leukemia (AML) cell line HL-60, and to explore the molecular mechanism of Olaparib on HL-60 cells.@*METHODS@#After HL-60 cells in logarithmic growth phase were treated with Olaparib at different concentrations for different times (24, 48 h), the expression of NKG2D ligand on the surface of HL-60 cells was detected by flow cytometry. Western blot was used to dectect the expression of ERK expression in HL-60 cells. The killing effect of NK cells to HL-60 cells was detected by CFSE/PI method.@*RESULTS@#10 μmol/L Olaparib could upregulate the expression of NKG2D ligand on the surface of HL-60 cell at 24 and 48 hours, while 5 μmol/L Olaparib could induce up-regulation of the expression of ULBP-2 and ULBP-3 at 48 hours. Western blot analysis showed that ERK phosphorylation of HL-60 cells was enhanced after treating with Olaparib. The killing effect of NK cells to HL-60 cells could be enhanced by Olaparib, however, ERK inhibitor could suppress the killing effect of NK cells to HL-60 cells.@*CONCLUSION@#Olaparib can upregulate NKG2D ligands expression on the surface of HL-60 cells and enhance the cytotoxicity of NK cell to HL-60 cells. The mechanism may be related to Olaparib promoting ERK phosphorylation expression.
Assuntos
Texto completo: 1 Base de dados: WPRIM Assunto principal: Ftalazinas / Piperazinas / Antígenos de Histocompatibilidade Classe I / Células HL-60 / Citotoxicidade Imunológica / Linhagem Celular Tumoral / Subfamília K de Receptores Semelhantes a Lectina de Células NK / Inibidores de Poli(ADP-Ribose) Polimerases / Ligantes Limite: Humans Idioma: Zh Ano de publicação: 2020 Tipo de documento: Article
Texto completo: 1 Base de dados: WPRIM Assunto principal: Ftalazinas / Piperazinas / Antígenos de Histocompatibilidade Classe I / Células HL-60 / Citotoxicidade Imunológica / Linhagem Celular Tumoral / Subfamília K de Receptores Semelhantes a Lectina de Células NK / Inibidores de Poli(ADP-Ribose) Polimerases / Ligantes Limite: Humans Idioma: Zh Ano de publicação: 2020 Tipo de documento: Article