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随着年龄增长,T细胞比B细胞更容易发生脂质过氧化并积累荧光产物。

Susceptibility to lipid peroxidation and accumulation of fluorescent products with age is greater in T-cells than B-cells.

作者信息

Hendricks L C, Heidrick M L

机构信息

Department of Biochemistry, University of Nebraska College of Medicine, Omaha 68105.

出版信息

Free Radic Biol Med. 1988;5(3):145-54. doi: 10.1016/0891-5849(88)90077-9.

Abstract

The age-related loss of immune function, which is primarily due to loss of T-lymphocyte function, is also associated with accumulation in spleen lymphocytes of autofluorescent products indicative of peroxidation damage. In this study, we examined T-cell membranes for age-related changes which could be related to lipid peroxidation. Using fluorescence spectroscopy of CHCl3:CH3OH membrane extracts, we observed that old T-cells have a 2-fold greater accumulation of fluorescent products than old B-cells and that young T-cells, when exposed to free radicals in an in vitro system, accumulate significantly more fluorescent products over time than young B-cells. We used fluorescence polarization to show that young T-cell membranes are more fluid than young B-cell membranes. However, T-cell membrane fluidity decreases with age, whereas B-cell membrane fluidity does not change; in old mice, T-cell membranes are significantly less fluid than old B-cell membranes. Using two-dimensional electrophoresis, we showed that membrane extracts of old T-cells contain many more proteins than extracts of young T-cells. Our results indicate that age-related changes occur in T-cell membranes which could be due to their increased susceptibility to lipid peroxidation and these changes may contribute to the age-related decline in immune function.

摘要

与年龄相关的免疫功能丧失主要是由于T淋巴细胞功能丧失,这也与脾脏淋巴细胞中指示过氧化损伤的自发荧光产物的积累有关。在本研究中,我们检查了T细胞膜与年龄相关的变化,这些变化可能与脂质过氧化有关。使用CHCl3:CH3OH膜提取物的荧光光谱法,我们观察到老年T细胞中荧光产物的积累比老年B细胞多2倍,并且在体外系统中,年轻T细胞在暴露于自由基时,随着时间的推移比年轻B细胞积累显著更多的荧光产物。我们使用荧光偏振表明,年轻T细胞膜比年轻B细胞膜更具流动性。然而,T细胞膜流动性随年龄增长而降低,而B细胞膜流动性不变;在老年小鼠中,T细胞膜的流动性明显低于老年B细胞膜。使用二维电泳,我们表明老年T细胞的膜提取物比年轻T细胞的提取物含有更多的蛋白质。我们的结果表明,T细胞膜中发生了与年龄相关的变化,这可能是由于它们对脂质过氧化的敏感性增加,并且这些变化可能导致与年龄相关的免疫功能下降。

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