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蛋白酶体抑制剂MG132诱导KG-1细胞凋亡的机制研究
  • 期刊名称:浙江理工大学学报
  • 时间:0
  • 页码:597-601
  • 语言:中文
  • 分类:Q789[生物学—分子生物学]
  • 作者机构:[1]浙江理工大学生命科学学院新元医学与生物技术研究所,杭州310018
  • 相关基金:国家自然科学基金(30801379); 浙江省“生物医学工程”重中之重学科开放基金(SWYX0804 SWYX0812)
  • 相关项目:通过急性髓性白血病干细胞表面CD123导入溶瘤腺病毒的实验研究
中文摘要:

研究蛋白酶体抑制剂MG132对人急性髓性白血病细胞株KG-1的致凋亡作用及其对细胞内信号传导因子NF-κB与凋亡蛋白PARP表达的影响。采用CCK-8法检测MG132对KG-1细胞增殖的抑制作用;利用Hoechst33342染色法,从形态学上观察凋亡的KG-1细胞;Western blot检测NF-κB活性及与凋亡相关的蛋白变化情况。CCK-8法检测结果表明,MG132能明显抑制KG-1细胞生长,并呈现时间依赖性和浓度依赖性;Hoechst染色和Western blot检测实验证明,MG132诱导KG-1细胞发生凋亡的同时,NF-κB活性明显降低,细胞凋亡蛋白PARP降解为P89蛋白。以上结果显示,MG132能诱导KG-1细胞凋亡,其机制可能与MG132抑制NF-κB信号转导通路,下调NF-κB表达继而增加凋亡蛋白PARP剪切有关。

英文摘要:

The study is aimed to explore the apoptosis effect of proteasome inhibitor MG132 on human acute myeloid leukemia(AML) cell line KG-1 and the expression of nuclear factor-kappa B(NF-κB) and the apoptotic signaling pathway protein.CCK-8 assay tests the growth inhibition effect of MG132 on KG-1 cell;the apoptosis of KG-1 cells induced by MG132 is observed through Hoechst 33342 staining under fluorescent microscope;the NF-κB activity and the expression of apoptotic signaling pathway protein are found by Western blot analysis.CCK-8 assay shows that the growth of KG-1 cell was inhibited by MG132 and presented double manners of concentration and time dependence;the Hoechst 33342 staining and Western blot analysis indicated that the activity of NF-κB is decreased by MG132 on KG-1 cell,and the apoptotic signaling pathway protein PARP is cleaved to a 89KD protein.All the results confirmed that MG132 can obviously inhibit the growth of KG-1 cells,and the possible mechanism was that the apoptotic signaling pathway of NF-κB is inhibited by MG132 and the low expression of NF-κB in turn increasing the apoptotic protein PARP cleavage.

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