内化
胞浆
细胞生物学
癌细胞
溶酶体
组织蛋白酶B
纳米颗粒
程序性细胞死亡
表皮生长因子受体
生物物理学
自噬
组织蛋白酶
材料科学
共焦显微镜
表皮生长因子
组织蛋白酶D
细胞内
化学
生物
细胞
氧化铁纳米粒子
细胞凋亡
受体
癌症
生物化学
纳米技术
酶
遗传学
作者
Maribella Domenech,Ileana Marrero-Berríos,Madeline Torres‐Lugo,Carlos Rinaldi
出处
期刊:ACS Nano
[American Chemical Society]
日期:2013-05-22
卷期号:7 (6): 5091-5101
被引量:261
摘要
Lysosomal death pathways are being explored as alternatives of overcoming cancer tumor resistance to traditional forms of treatment. Nanotechnologies that can selectively target and induce permeabilization of lysosomal compartments in cells could become powerful medical tools. Here we demonstrate that iron oxide magnetic nanoparticles (MNPs) targeted to the epidermal growth factor receptor (EGFR) can selectively induce lysosomal membrane permeabilization (LMP) in cancer cells overexpressing the EGFR under the action of an alternating magnetic field (AMF). LMP was observed to correlate with the production of reactive oxygen species (ROS) and a decrease in tumor cell viability. Confocal microscopy images showed an increase in the cytosolic activity of the lysosomal protease cathepsin B. These observations suggest the possibility of remotely triggering lysosomal death pathways in cancer cells through the administration of MNPs which target lysosomal internalization pathways and the application of AMFs.
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