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Medin:主动脉平滑肌细胞产生的乳粘连蛋白的一个完整片段构成了最常见的人类淀粉样蛋白。

Medin: an integral fragment of aortic smooth muscle cell-produced lactadherin forms the most common human amyloid.

作者信息

Häggqvist B, Näslund J, Sletten K, Westermark G T, Mucchiano G, Tjernberg L O, Nordstedt C, Engström U, Westermark P

机构信息

Division of Molecular and Immunological Pathology and Cell Biology, Linköping University, S-581 85 Linköping, Sweden.

出版信息

Proc Natl Acad Sci U S A. 1999 Jul 20;96(15):8669-74. doi: 10.1073/pnas.96.15.8669.

Abstract

Aortic medial amyloid is a form of localized amyloid that occurs in virtually all individuals older than 60 years. The importance and impact of the amyloid deposits are unknown. In this study we have purified a 5.5-kDa aortic medial amyloid component, by size-exclusion chromatography and RP-HPLC, from three individuals, and we have shown by amino acid sequence analysis that the amyloid is derived from an integral proteolytic fragment of lactadherin. Lactadherin is a 364-aa glycoprotein, previously known to be expressed by mammary epithelial cells as a cell surface protein and secreted as part of the milk fat globule membrane. The multidomain protein has a C-terminal domain showing homology to blood coagulation factors V and VIII. We found that the main constituent of aortic medial amyloid is a 50-aa-long peptide, here called medin, that is positioned within the coagulation factor-like domain of lactadherin. Our result is supported by the specific labeling of aortic medial amyloid in light and electron microscopy with two rabbit antisera raised against two synthetic peptides corresponding to different parts of medin. By using in situ hybridization we have shown that lactadherin is expressed by aortic medial smooth muscle cells. Furthermore, one of the synthetic peptides forms amyloid-like fibrils in vitro. Lactadherin was not previously known to be an amyloid precursor protein or to be expressed in aortic tissue. The structure of lactadherin may implicate an important regulatory function in the aorta.

摘要

主动脉中层淀粉样蛋白是一种局限性淀粉样蛋白,几乎所有60岁以上的个体都会出现。淀粉样蛋白沉积物的重要性和影响尚不清楚。在本研究中,我们通过尺寸排阻色谱法和反相高效液相色谱法从三名个体中纯化了一种5.5 kDa的主动脉中层淀粉样蛋白成分,并通过氨基酸序列分析表明,该淀粉样蛋白源自乳粘连蛋白的一个完整蛋白水解片段。乳粘连蛋白是一种364个氨基酸的糖蛋白,以前已知由乳腺上皮细胞作为细胞表面蛋白表达,并作为乳脂肪球膜的一部分分泌。这种多结构域蛋白的C末端结构域与凝血因子V和VIII具有同源性。我们发现主动脉中层淀粉样蛋白的主要成分是一种50个氨基酸长的肽,在此称为medin,它位于乳粘连蛋白的凝血因子样结构域内。用针对medin不同部分的两种合成肽制备的两种兔抗血清对主动脉中层淀粉样蛋白进行光镜和电镜下的特异性标记,支持了我们的结果。通过原位杂交,我们表明乳粘连蛋白由主动脉中层平滑肌细胞表达。此外,其中一种合成肽在体外形成淀粉样纤维。以前不知道乳粘连蛋白是一种淀粉样前体蛋白或在主动脉组织中表达。乳粘连蛋白的结构可能在主动脉中具有重要的调节功能。

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