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基底膜胶原 IV 缺乏促进腹主动脉瘤形成。

Basement membrane collagen IV deficiency promotes abdominal aortic aneurysm formation.

机构信息

Centre for Individualized Medicine in Artery Diseases, Odense University Hospital, J. B. Winsløws Vej 4, 5000, Odense C, Denmark.

Department of Molecular Medicine, University of Southern Denmark, Odense, Denmark.

出版信息

Sci Rep. 2021 Jun 18;11(1):12903. doi: 10.1038/s41598-021-92303-y.

DOI:10.1038/s41598-021-92303-y
PMID:34145342
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8213747/
Abstract

Abdominal aortic aneurysm (AAA) is a complex disease which is incompletely accounted for. Basement membrane (BM) Collagen IV (COL4A1/A2) is abundant in the artery wall, and several lines of evidence indicate a protective role of baseline COL4A1/A2 in AAA development. Using Col4a1/a2 hemizygous knockout mice (Col4a1/a2, 129Svj background) we show that partial Col4a1/a2 deficiency augmented AAA formation. Although unchallenged aortas were morphometrically and biomechanically unaffected by genotype, explorative proteomic analyses of aortas revealed a clear reduction in BM components and contractile vascular smooth muscle cell (VSMC) proteins, suggesting a central effect of the BM in maintaining VSMCs in the contractile phenotype. These findings were translated to human arteries by showing that COL4A1/A2 correlated to BM proteins and VSMC markers in non-lesioned internal mammary arteries obtained from coronary artery bypass procedures. Moreover, in human AAA tissue, MYH11 (VSMC marker) was depleted in areas of reduced COL4 as assessed by immunohistochemistry. Finally, circulating COL4A1 degradation fragments correlated with AAA progression in the largest Danish AAA cohort, suggesting COL4A1/A2 proteolysis to be an important feature of AAA formation. In sum, we identify COL4A1/A2 as a critical regulator of VSMC phenotype and a protective factor in AAA formation.

摘要

腹主动脉瘤 (AAA) 是一种复杂的疾病,其发病机制尚不完全清楚。基底膜 (BM) 中的胶原 IV (COL4A1/A2) 在动脉壁中含量丰富,有几方面的证据表明基线 COL4A1/A2 在 AAA 发展中起保护作用。使用 Col4a1/a2 半合子敲除小鼠 (Col4a1/a2, 129Svj 背景),我们发现部分 Col4a1/a2 缺失会增强 AAA 的形成。尽管主动脉在形态和生物力学上不受基因型影响,但对主动脉的探索性蛋白质组分析显示 BM 成分和收缩性血管平滑肌细胞 (VSMC) 蛋白明显减少,表明 BM 在维持 VSMC 收缩表型方面起着核心作用。这些发现通过显示 COL4A1/A2 与非病变内乳动脉中的 BM 蛋白和 VSMC 标志物在取自冠状动脉旁路手术的非病变内乳动脉中相关而转化为人类动脉。此外,在人 AAA 组织中,通过免疫组织化学评估,COL4 减少的区域中 MYH11 (VSMC 标志物) 耗竭。最后,循环 COL4A1 降解片段与丹麦最大的 AAA 队列中的 AAA 进展相关,提示 COL4A1/A2 蛋白水解是 AAA 形成的一个重要特征。总之,我们确定 COL4A1/A2 是 VSMC 表型的关键调节因子和 AAA 形成的保护因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0784/8213747/c75535a5537c/41598_2021_92303_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0784/8213747/d043125e2940/41598_2021_92303_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0784/8213747/a8f86dda18cd/41598_2021_92303_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0784/8213747/b0eae38a7d3c/41598_2021_92303_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0784/8213747/c75535a5537c/41598_2021_92303_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0784/8213747/d043125e2940/41598_2021_92303_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0784/8213747/a8f86dda18cd/41598_2021_92303_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0784/8213747/b0eae38a7d3c/41598_2021_92303_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0784/8213747/c75535a5537c/41598_2021_92303_Fig4_HTML.jpg

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