摘要
目的:采用ox-LDL诱导巨噬细胞泡沫化模型,通过不同剂量衣霉素诱导巨噬细胞不同程度内质网应激,观察对其自噬的影响。方法:不同剂量衣霉素作用于小鼠巨噬细胞系RAW264.7,通过TUNEL染色检测其凋亡率,Western blot检测内质网应激蛋白GRP78,以及自噬标志蛋白P62的表达水平。结果:与ox-LDL组和大剂量衣霉素组相比,小剂量衣霉素组可以显著减少巨噬细胞的凋亡(P<0.01);与ox-LDL组相比,小剂量衣霉素组上调内质网应激蛋白GRP78表达的同时,自噬标志蛋白P62适度下降(P<0.01);大剂量衣霉素组更为显著地上调了内质网应激蛋白GRP78表达,但同时自噬标志蛋白P62也显著增加(P<0.01)。结论:小剂量衣霉素引起一定程度的内质网应激,可以激活适度的自噬,从而减少巨噬细胞的凋亡,可能有助于降低动脉粥样硬化的程度。
Objective： By using ox-LDL-indueed macrophage foam cell model, we used different doses of tunicamycin to induce different degree of the endoplasmic reticulum stress, to observe the effects of it on autophagy. Methods： Different doses of tunieamycin were added to maerophage RAW264.7. The apoptosis rate was detected with TUNEL method. And the expression level of the endoplasmic reticulum stress marker protein GRP78 and autophagy marker protein P62 were detected by western blotting. Results： Compared with the ox-LDL group and the high-dose ttmicamycin group, low-dose of tunieamycin significantly reduced the apoptosis of macrophage （P〈0.01）; compared with ox-LDL group, the endoplasmic reticulum stress marker protein GRP78 expression was remarkable increased in low-dose tunicamycin group; meanwhile, the autophagy marker protein P62 moderately decreased （P〈0.01）; in the high-dose ttmicamycin group, there was more significant increase in the endoplasmic reticulurn stress marker protein GRP78 expression, however the autophagy marker protein P62 also increased notably （P〈0.01）. Conclusion： Low-dose of tunicamycin caused a certain degree of endoplasmic reticulum stress, which activated moderate autophagy, decreasing macrophage apoptosis. It may help to reduce the extent of the atherosclerosis.
出处
《现代生物医学进展》
CAS
2014年第2期209-213,共5页
Progress in Modern Biomedicine
基金
国家自然科学基金项目(81170184)
陕西省社会发展公关计划课题(2012SF2-02-3)
作者简介
马美娟（1987-），女，硕士，动脉粥样硬化，Tel：13310988552，E—mail：dyrnameijuan@163．com
通讯作者：李妍，电话：13892890227，E-mail：fireman．finmu@edu．cn
