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Different susceptibilities to cell death induced by t-butylhydroperoxide could depend upon cell histotype-associated growth features.

作者信息

Malorni W, Rainaldi G, Rivabene R, Santini M T

机构信息

Department of Ultrastructures, Istituto Superiore di Sanità, Rome, Italy.

出版信息

Cell Biol Toxicol. 1994 Aug;10(4):207-18. doi: 10.1007/BF00756761.

DOI:10.1007/BF00756761
PMID:7895150
Abstract

The effects of the oxidizing agent t-butylhydroperoxide (t-BHP) were investigated on three human cell lines of different origin and growth features (A431 epithelial cells, ADF astrocytoma cells and U937 leukemic cells) using electron microscopy and electron paramagnetic resonance spectroscopy. The results indicate that important biophysical and ultrastructural modifications are induced in the plasma and mitochondrial membranes of these cells and that these changes can ultimately lead to cell death. In addition, the cell cytoskeleton also appears to be a target of hydroperoxide-mediated stress. In particular, all three cell types undergo cytoskeletal alterations leading to surface blebbing, a typical characteristic of cell damage. However, the timing and extent of this damage as well as that occurring at the mitochondrial and plasma membrane levels seems to be different: cells with weak (ADF) or absent (U937) cell-to-cell and cell-substrate contacts and a poorly developed cytoskeleton appear to be more susceptible than other cell types (e.g., A431) to t-BHP-mediated injury. These diverse cell susceptibilites to hydroperoxide-mediated oxidative stress could thus depend upon cell histotype-associated growth features.

摘要

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A new, striking morphologic feature for the human erythrocyte in hereditary spherocytosis: the blebbing pattern.遗传性球形红细胞增多症中人类红细胞的一种新的显著形态学特征:泡状模式。
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Free radicals in disease processes: a compilation of cause and consequence.
激酶抑制剂 SI113 诱导自噬,并与氯喹嗪协同作用抑制人多形性胶质母细胞瘤细胞的生长。
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The small molecule SI113 synergizes with mitotic spindle poisons in arresting the growth of human glioblastoma multiforme.小分子SI113与有丝分裂纺锤体毒物协同作用,可抑制多形性胶质母细胞瘤的生长。
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SI113, a SGK1 inhibitor, potentiates the effects of radiotherapy, modulates the response to oxidative stress and induces cytotoxic autophagy in human glioblastoma multiforme cells.SI113是一种SGK1抑制剂,可增强放射治疗的效果,调节对氧化应激的反应,并在多形性胶质母细胞瘤细胞中诱导细胞毒性自噬。
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