Division of Experimental Pathology, Department of Clinical and Experimental Medicine, Faculty of Health Sciences, Linkoping University, Linköping, Sweden.
FEBS Lett. 2011 Feb 18;585(4):623-9. doi: 10.1016/j.febslet.2010.12.043. Epub 2011 Jan 8.
Moderate lysosomal membrane permeabilization (LMP) is an important inducer of apoptosis. Macrophages are professional scavengers and are rich in hydrolytic enzymes and iron. In the present study, we found that LMP by lysosomotropic detergent MSDH resulted in early up-regulation of lysosomal cathepsins, oxidative stress and ferritin up-regulation, and cell death. Lysosomotropic base NH(4)Cl reduced the ferritin induction and oxidative stress in apoptotic cells induced by MSDH. Cysteine cathepsin inhibitors significantly protected cell death and oxidative stress, but had less effect on ferritin induction. We conclude that oxidative stress induced by lysosomal rupture causes ferritin induction with concomitant mitochondrial damage, which are the potential target for prevention of cellular oxidative stress and cell death induced by typical lysosomotropic substances in different disorders.
中等程度的溶酶体膜通透性(LMP)是细胞凋亡的重要诱导因素。巨噬细胞是专业的吞噬细胞,富含各种水解酶和铁。在本研究中,我们发现溶酶体载体 MSDH 引起的 LMP 导致溶酶体组织蛋白酶早期上调、氧化应激和铁蛋白上调,以及细胞死亡。溶酶体碱 NH4Cl 降低了 MSDH 诱导的细胞凋亡中 ferritin 的诱导和氧化应激。半胱氨酸组织蛋白酶抑制剂显著保护细胞死亡和氧化应激,但对 ferritin 的诱导影响较小。我们的结论是,溶酶体破裂引起的氧化应激导致 ferritin 的诱导,并伴有线粒体损伤,这可能是预防不同疾病中典型溶酶体物质引起的细胞氧化应激和细胞死亡的潜在靶点。