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首页> 外文期刊>Experimental Gerontology >Ceroid/lipofuscin-loaded human fibroblasts show increased susceptibility to oxidative stress.
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Ceroid/lipofuscin-loaded human fibroblasts show increased susceptibility to oxidative stress.

机译:负载了类固醇/脂褐素的人成纤维细胞显示出对氧化应激的敏感性增加。

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摘要

To test whether the possibly enhanced sensitivity of aged cells to oxidative stress may depend on their content of ceroid/lipofuscin, AG-1518 human fibroblasts with various amounts of the pigment accumulated due to prolonged cultivation under normobaric hyperoxia were exposed to acute oxidative stress (2.5 microM naphthazarin, 15 min) and then returned to standard culture conditions. Twenty-four hours after the naphthazarin treatment, 37% of the cells were still vital, whereas others had undergone oxidative stress-induced apoptosis with ensuing postapoptotic necrosis. The average amount of ceroid/lipofuscin within the surviving cells was only about half of that of the initial population of cells, as measured before the naphthazarin exposure. This finding suggests that ceroid/lipofuscin-rich cells have an increased sensitivity to oxidative stress. The ceroid/lipofuscin quantity strongly positively correlated with the size of the acidic compartment (as evaluated by uptake of the weakly basic lysosomotropic fluorochrome acridine orange) and with its content of the lysosomal protease cathepsin D, as assayed by immunocytochemistry. We hypothesize that the enhanced sensitivity of ceroid/lipofuscin-loaded cells to oxidative stress may be caused by the increased amounts of lysosomal enzymes, known as mediators of oxidative damage, and/or by catalysis of intralysosomal oxidative reactions by lipofuscin-associated iron.
机译:为了测试衰老细胞对氧化应激的敏感性是否可能取决于其类固醇/脂褐素的含量,将在常压高氧下长时间培养而积累了各种色素的AG-1518人成纤维细胞暴露于急性氧化应激下(2.5 microM naphthazarin,15分钟),然后返回标准培养条件。萘他沙林处理后二十四小时,仍然有37%的细胞保持活力,而其他细胞则经历了氧化应激诱导的细胞凋亡,并随之发生凋亡后坏死。萘普沙林暴露前测得,存活细胞中的类固醇/脂褐素的平均含量仅为初始细胞数量的一半。这一发现表明富含类固醇/脂褐素的细胞对氧化应激的敏感性增加。如通过免疫细胞化学分析,类固醇/脂褐素的量与酸性区室的大小(通过吸收弱碱性溶血同性荧光色素tropic啶橙评估)和其溶酶体蛋白酶组织蛋白酶D的含量成正相关。我们假设,负载类固醇/脂褐素的细胞对氧化应激的敏感性增强可能是由于溶酶体酶(被称为氧化损伤的介质)的数量增加和/或脂溶素相关铁催化的溶酶体内氧化反应所致。

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