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腹主动脉瘤近段至远段金属蛋白酶及其抑制剂的表达梯度。

Expression gradient of metalloproteinases and their inhibitors from proximal to distal segments of abdominal aortic aneurysm.

机构信息

Department of Molecular Biology, Faculty of Medical Science in Katowice, Medical University of Silesia, Katowice, Poland.

Department of Medical Genetics, Faculty of Medical Science in Katowice, Medical University of Silesia, Katowice, Poland.

出版信息

J Appl Genet. 2021 Sep;62(3):499-506. doi: 10.1007/s13353-021-00642-3. Epub 2021 Jun 6.

Abstract

Abdominal aortic aneurysm refers to abnormal, asymmetric distension of the infrarenal aortic wall due to pathological remodelling of the extracellular matrix. The distribution of enzymes remodelling the extracellular matrix and their expression patterns in the affected tissue are largely unknown. The goal of this work was to investigate the expression profiles of 20 selected genes coding for metalloproteinases and their inhibitors in the proximal to the distal direction of the abdominal aortic aneurysm. RNA samples were purified from four lengthwise fragments of aneurysm and border tissue obtained from 29 patients. The quantities of selected mRNAs were determined by real-time PCR to reveal the expression patterns. The genes of interest encode collagenases (MMP1, MMP8, MMP13), gelatinases (MMP2, MMP9), stromelysins (MMP3, MMP7, MMP10, MMP11, MMP12), membrane-type MMPs (MMP14, MMP15, MMP16), tissue inhibitors of metalloproteinases (TIMP1, TIMP2, TIMP3, TIMP4), and ADAMTS proteinases (ADAMTS1, ADAMTS8, and ADAMTS13). It was found that MMP, TIMP, and ADAMTS are expressed in all parts of the aneurysm with different patterns. A developed aneurysm has such a disturbed expression of the main participants in extracellular matrix remodelling that it is difficult to infer the causes of the disorder development. MMP12 secreted by macrophages at the onset of inflammation may initiate extracellular matrix remodelling, which, if not controlled, initiates a feedback loop leading to aneurysm formation.

摘要

腹主动脉瘤是指由于细胞外基质的病理性重塑,导致肾下主动脉壁的异常、不对称扩张。细胞外基质重塑的酶的分布及其在病变组织中的表达模式在很大程度上尚不清楚。本工作的目的是研究 20 个选定的编码金属蛋白酶及其抑制剂的基因在腹主动脉瘤的近-远方向上的表达谱。从 29 名患者获得的动脉瘤和边界组织的四个纵向片段中纯化 RNA 样本。通过实时 PCR 确定所选 mRNA 的量以揭示表达模式。感兴趣的基因编码胶原酶(MMP1、MMP8、MMP13)、明胶酶(MMP2、MMP9)、基质金属蛋白酶(MMP3、MMP7、MMP10、MMP11、MMP12)、膜型 MMPs(MMP14、MMP15、MMP16)、金属蛋白酶组织抑制剂(TIMP1、TIMP2、TIMP3、TIMP4)和 ADAMTS 蛋白酶(ADAMTS1、ADAMTS8 和 ADAMTS13)。研究发现 MMP、TIMP 和 ADAMTS 在动脉瘤的所有部位都有不同模式的表达。一个已经发展的动脉瘤对细胞外基质重塑的主要参与者的表达如此紊乱,以至于很难推断出紊乱发展的原因。炎症开始时巨噬细胞分泌的 MMP12 可能启动细胞外基质重塑,如果不受控制,就会启动一个反馈回路,导致动脉瘤形成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4eea/8357691/3e6cb2581b9f/13353_2021_642_Fig1_HTML.jpg

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