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晚期糖基化终末产物受体在周围闭塞性血管疾病中的表达

Expression of receptors for advanced glycation end products in peripheral occlusive vascular disease.

作者信息

Ritthaler U, Deng Y, Zhang Y, Greten J, Abel M, Sido B, Allenberg J, Otto G, Roth H, Bierhaus A

机构信息

Department of Medicine, University of Heidelberg, Germany.

出版信息

Am J Pathol. 1995 Mar;146(3):688-94.

Abstract

The cellular interactions of advanced glycation end products (AGEs), which have been hypothesized to contribute to the development of vascular lesions, occur, at least in part, through their binding to a novel integral membrane protein, the receptor for AGEs (RAGE). Studies of human vascular segments show that endothelial RAGE expression at the antigen and mRNA level was variable and usually at low levels in samples from healthy individuals. In contrast, patients with a range of peripheral occlusive vascular diseases, with or without underlying diabetes, demonstrated prominent enhancement of endothelial RAGE expression. Smooth muscle cells and nerves in the vessel wall showed constitutively high levels of RAGE expression that were unchanged with aging (from 1 to 92 years) or by the presence of vascular disease. These data suggest that RAGE is likely to have ligands other than AGEs, and that multiple factors in addition to AGEs impact on its expression. Taken together, our findings suggest that RAGE may contribute to the pathogenesis of a range of vascular disorders.

摘要

晚期糖基化终末产物(AGEs)的细胞相互作用被认为与血管病变的发展有关,至少部分是通过它们与一种新型整合膜蛋白——AGEs受体(RAGE)的结合来实现的。对人体血管段的研究表明,在健康个体的样本中,内皮RAGE在抗原和mRNA水平的表达是可变的,且通常处于低水平。相比之下,患有一系列外周闭塞性血管疾病的患者,无论是否伴有潜在糖尿病,其内皮RAGE表达均显著增强。血管壁中的平滑肌细胞和神经显示出RAGE的组成性高表达,其表达水平不会随年龄增长(从1岁到92岁)或血管疾病的存在而改变。这些数据表明,RAGE可能有除AGEs之外的配体,并且除AGEs外,多种因素也会影响其表达。综上所述,我们的研究结果表明,RAGE可能在一系列血管疾病的发病机制中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/194b/1869189/d0d74f9e2fcb/amjpathol00051-0147-a.jpg

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