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亚历山大病中的晚期脂质过氧化终产物

Advanced lipid peroxidation end-products in Alexander's disease.

作者信息

Castellani R J, Perry G, Harris P L, Cohen M L, Sayre L M, Salomon R G, Smith M A

机构信息

Department of Pathology, University of Maryland Medical Center, 22 South Greene Street, Baltimore, MD 21201, USA.

出版信息

Brain Res. 1998 Mar 16;787(1):15-8. doi: 10.1016/s0006-8993(97)01224-9.

Abstract

Rosenthal fibers (RF), intra-astrocytic hyaline inclusions, accumulate in various pathological conditions and are the histological hallmark of Alexander's disease. While the major protein components of RF have been identified, the factors accounting for their pathogenesis, accumulation, and insolubility are largely unknown. In this study, we immunohistochemically examined three cases of Alexander's disease using antibodies to a lysine-derived pyrrole modification arising from 4-hydroxy-2-nonenal, a highly cytotoxic reactive aldehyde produced by lipid peroxidation. In all the cases of Alexander's disease examined, strong immunolabeling of RF by the antibodies to 4-hydroxy-2-nonenal pyrrole adducts were noted. By contrast, age-matched control cases showed no immunoreactivity. These results indicate that modification of protein by lipid peroxidation adducts may play an important role in the formation of RF as well as in the pathogenesis of Alexander's disease. Furthermore, taken together with our previous data indicating advanced Maillard reaction end products in RF, it seems that post-translational modification of RF, initiated by oxidative stress, is critical for both the accumulation and the insolubility of RF, and therefore, by inference, in the pathogenesis of Alexander's disease.

摘要

罗森塔尔纤维(RF)是星形细胞内的透明包涵体,在多种病理情况下会积聚,是亚历山大病的组织学标志。虽然RF的主要蛋白质成分已被确定,但其发病机制、积聚及不溶性的相关因素在很大程度上仍不清楚。在本研究中,我们使用针对由4-羟基-2-壬烯醛(一种脂质过氧化产生的高细胞毒性反应性醛)衍生的赖氨酸吡咯修饰的抗体,对3例亚历山大病进行了免疫组织化学检查。在所检查的所有亚历山大病病例中,均观察到针对4-羟基-2-壬烯醛吡咯加合物的抗体对RF有强烈的免疫标记。相比之下,年龄匹配的对照病例未显示免疫反应性。这些结果表明,脂质过氧化加合物对蛋白质的修饰可能在RF的形成以及亚历山大病的发病机制中起重要作用。此外,结合我们之前表明RF中存在晚期美拉德反应终产物的数据,似乎由氧化应激引发的RF翻译后修饰对于RF的积聚和不溶性至关重要,因此,由此推断,对亚历山大病的发病机制也至关重要。

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