镉对细胞自噬、凋亡和细胞器的影响。

C. S. Vergílio, E. D. de Melo
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引用次数: 12

摘要

镉(Cd)在不同的组织中引起几种作用,但我们对其对细胞器的毒性作用的认识还不够。为了观察Cd对细胞器结构和功能影响的进展,我们将HuH-7细胞(人肝癌细胞系)暴露在CdCl2浓度(1微米- 20微米)和暴露时间(2小时- 24小时)增加的环境中。在Cd处理过程中,细胞的活力表现出时间和剂量依赖性的逐渐下降。Cd处理的细胞表现出进行性的形态学改变,包括细胞质收缩和细胞核凝聚,直至完全丧失细胞粘附。10 μ m处理12 h可导致不可逆损伤。在这些剧烈和不可修复的损伤之前,处理细胞(5微米12小时)表现出线粒体功能的进行性丧失和细胞质酸化,以及微丝和内质网的功能障碍和解体。这些损伤导致凋亡事件的诱导和细胞质中自噬小体的增加。这些结果表明,Cd影响多种细胞内靶点,诱导线粒体、细胞骨架、内质网和酸性室的改变,最终通过凋亡和自噬途径导致细胞死亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Autophagy, apoptosis and organelle features during cell exposure to cadmium.
Cadmium (Cd) induces several effects in different tissues, but our knowledge of the toxic effects on organelles is insufficient. To observe the progression of Cd effects on organelle structure and function, HuH-7 cells (human hepatic carcinoma cell line) were exposed to CdCl2 in increasing concentrations (1 microM - 20 microM) and exposure times (2 h - 24 h). During Cd treatment, the cells exhibited a progressive decrease in viability that was both time- and dose-dependent. Cd treated cells displayed progressive morphological changes that included cytoplasm retraction and nuclear condensation preceding a total loss of cell adhesion. Treatment with 10 microM for 12 h led to irreversible damages. Before these drastic and irreparable damages, treated cells (5 microM for 12 h) presented a progressive loss of mitochondrial function and cytoplasm acidification as well as dysfunction and disorganization of microfilaments and endoplasmic reticulum. These damages led to the induction of apoptotic events and an increase in autophagic bodies in the cytoplasm. These results revealed that Cd affects multiple intra-cellular targets that induce alterations in the mitochondria, cytoskeleton, endoplasmic reticulum and acidic compartments, ultimately culminating in cell death via apoptotic and autophagic pathways.
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