中南医学科学杂志
中南醫學科學雜誌
중남의학과학잡지
JOURNAL OF UNIVERSITY OF SOUTH CHINA(MEDICAL EDITION)
2014年
3期
217-221
,共5页
白洁%孟军%刘艳辉%李小红%危当恒
白潔%孟軍%劉豔輝%李小紅%危噹恆
백길%맹군%류염휘%리소홍%위당항
Ox-LDL%THP-1巨噬细胞%自噬
Ox-LDL%THP-1巨噬細胞%自噬
Ox-LDL%THP-1거서세포%자서
oxidized low density lipoprotein%THP-1 macrophage%autophagy
目的探讨氧化型低密度脂蛋白( Ox-LDL)对PMA诱导的THP-1巨噬细胞自噬的影响。方法PMA诱导THP-1细胞24 h,使其分化为巨噬细胞,再分别用0、10、20、40或80 mg/L的Ox-LDL处理24 h,逆转录聚合酶链反应( RT-PCR)和免疫印迹技术( Western blotting)分别检测Beclin-1以及LC3的mRNA及蛋白表达;细胞免疫荧光检测LC3在细胞内的含量;MDC染色检测自噬囊泡的形成。结果随着Ox-LDL浓度的增加,THP-1源性巨噬细胞Beclin-1 mRNA及蛋白表达显著降低(P<0.05);LC3 mRNA表达无明显改变(P>0.05),但蛋白水平LC3II/LC3I显著降低(P<0.001);免疫荧光结果表明随着Ox-LDL浓度的增加,LC3II含量降低,MDC染色结果显示自噬囊泡随着Ox-LDL浓度的增加而减少。结论 Ox-LDL抑制PMA诱导的THP-1巨噬细胞自噬。
目的探討氧化型低密度脂蛋白( Ox-LDL)對PMA誘導的THP-1巨噬細胞自噬的影響。方法PMA誘導THP-1細胞24 h,使其分化為巨噬細胞,再分彆用0、10、20、40或80 mg/L的Ox-LDL處理24 h,逆轉錄聚閤酶鏈反應( RT-PCR)和免疫印跡技術( Western blotting)分彆檢測Beclin-1以及LC3的mRNA及蛋白錶達;細胞免疫熒光檢測LC3在細胞內的含量;MDC染色檢測自噬囊泡的形成。結果隨著Ox-LDL濃度的增加,THP-1源性巨噬細胞Beclin-1 mRNA及蛋白錶達顯著降低(P<0.05);LC3 mRNA錶達無明顯改變(P>0.05),但蛋白水平LC3II/LC3I顯著降低(P<0.001);免疫熒光結果錶明隨著Ox-LDL濃度的增加,LC3II含量降低,MDC染色結果顯示自噬囊泡隨著Ox-LDL濃度的增加而減少。結論 Ox-LDL抑製PMA誘導的THP-1巨噬細胞自噬。
목적탐토양화형저밀도지단백( Ox-LDL)대PMA유도적THP-1거서세포자서적영향。방법PMA유도THP-1세포24 h,사기분화위거서세포,재분별용0、10、20、40혹80 mg/L적Ox-LDL처리24 h,역전록취합매련반응( RT-PCR)화면역인적기술( Western blotting)분별검측Beclin-1이급LC3적mRNA급단백표체;세포면역형광검측LC3재세포내적함량;MDC염색검측자서낭포적형성。결과수착Ox-LDL농도적증가,THP-1원성거서세포Beclin-1 mRNA급단백표체현저강저(P<0.05);LC3 mRNA표체무명현개변(P>0.05),단단백수평LC3II/LC3I현저강저(P<0.001);면역형광결과표명수착Ox-LDL농도적증가,LC3II함량강저,MDC염색결과현시자서낭포수착Ox-LDL농도적증가이감소。결론 Ox-LDL억제PMA유도적THP-1거서세포자서。
Objective To explore the effect of oxidized low density lipoprotein ( Ox-LDL) on autophagy in THP-1-derived macrophages induced by phorbol-12-myristate-13-acetate ( PMA ) . Methods After treatment with PMA for 24 h,THP-1-derived macrophages were treated with 0,10,20,40 or 80 mg/L Ox-LDL for 24 h. Reverse transcription poly-merase chain reaction ( RT-PCR) and Western blotting were used to detect Beclin 1 and LC3 mRNA and protein expres-sion. Cell immunofluorescence was used to detect intracellular LC3II protein concentration. The autofluorescent substance monodansylcadaverine (MDC) was used to detect autophagic vacuoles (AVs). Results After treated with 0,10,20,40 or 80 mg/L Ox-LDL for 24 h,Beclin-1 mRNA and protein expression were obviously decreased(P<0. 05). There was no obvious change in LC3 mRNA expression (P>0. 05). However,the ratio of LC3II/LC3I was decreased with a concentration dependent manner at the level of protein (P<0. 001). Cell immunofluorescence showed that the intracellular LC3II concen-tration was decreased in response to Ox-LDL concentration. MDC staining showed that AVs had negative correlation with Ox-LDL concentration. Conclusion Ox-LDL inhibited PMA induced-THP-1 macrophage autophagy.