首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >AA-amyloidosis. Tissue component-specific association of various protein AA subspecies and evidence of a fourth SAA gene product.
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AA-amyloidosis. Tissue component-specific association of various protein AA subspecies and evidence of a fourth SAA gene product.

机译:AA淀粉样变性病。各种蛋白质AA亚种的组织成分特异性结合和第四个SAA基因产物的证据。

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摘要

Protein AA, the major repetitive protein subunit present in fibrils deposited in AA-amyloidosis, is an N-terminal cleavage product of a 104-amino acid precursor, serum amyloid A (SAA). Protein AA subspecies varying between 45 and 94 amino acids in length have been described. In this study it is shown that the different protein AA subspecies are not evenly distributed in amyloid deposits and that in single patients, certain subspecies of protein AA are deposited in specific tissue component sites. Thus larger protein AA subspecies occur in lower concentration in amyloid in the glomeruli compared to other sites and are especially found in amyloid in vessel walls. Three different SAA forms have been predicted from genomic and complementary DNA studies. The existence of a fourth type has been suspected from amino acid sequence studies of purified SAA. Protein AA derived from this fourth type of SAA is now shown to be present in amyloid fibrils in one of the patients studied in this paper.
机译:蛋白质AA是沉积在AA淀粉样变性病中的原纤维中的主要重复蛋白亚基,是104个氨基酸的前体血清淀粉样蛋白A(SAA)的N末端裂解产物。已经描述了长度在45至94个氨基酸之间变化的蛋白质AA亚种。在这项研究中表明,不同的蛋白质AA亚种在淀粉样蛋白沉积物中分布不均匀,并且在单例患者中,蛋白质AA的某些亚种沉积在特定的组织成分部位。因此,与其他部位相比,较大的蛋白质AA亚种在肾小球的淀粉样蛋白中的浓度较低,尤其是在血管壁的淀粉样蛋白中。从基因组和互补DNA研究中已预测出三种不同的SAA形式。从纯化的SAA的氨基酸序列研究中怀疑存在第四种类型。现在显示,在本文研究的一名患者中,淀粉样蛋白原纤维中存在第四种SAA衍生的蛋白质AA。

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