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Circ Res. 2016 Dec 9;119(12):1313-1323. doi: 10.1161/CIRCRESAHA.116.309799. Epub 2016 Sep 28.
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MYOSLID Is a Novel Serum Response Factor-Dependent Long Noncoding RNA That Amplifies the Vascular Smooth Muscle Differentiation Program.MYOSLID是一种新型的血清反应因子依赖性长链非编码RNA,可增强血管平滑肌分化程序。
Arterioscler Thromb Vasc Biol. 2016 Oct;36(10):2088-99. doi: 10.1161/ATVBAHA.116.307879. Epub 2016 Jul 21.
3
Smooth Muscle Enriched Long Noncoding RNA (SMILR) Regulates Cell Proliferation.平滑肌富集长链非编码RNA(SMILR)调节细胞增殖。
Circulation. 2016 May 24;133(21):2050-65. doi: 10.1161/CIRCULATIONAHA.115.021019. Epub 2016 Apr 6.
4
Vascular Smooth Muscle Cells in Atherosclerosis.动脉粥样硬化中的血管平滑肌细胞
Circ Res. 2016 Feb 19;118(4):692-702. doi: 10.1161/CIRCRESAHA.115.306361.
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Down-regulation of miR-23b induces phenotypic switching of vascular smooth muscle cells in vitro and in vivo.miR-23b 的下调可诱导血管平滑肌细胞体外和体内表型转换。
Cardiovasc Res. 2015 Sep 1;107(4):522-33. doi: 10.1093/cvr/cvv141. Epub 2015 May 20.
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Long noncoding RNAs in cardiovascular diseases.长链非编码 RNA 与心血管疾病
Circ Res. 2015 Feb 13;116(4):737-50. doi: 10.1161/CIRCRESAHA.116.302521.
7
Regulation of apoptosis by long non-coding RNA HIF1A-AS1 in VSMCs: implications for TAA pathogenesis.长链非编码RNA HIF1A-AS1对血管平滑肌细胞凋亡的调控:对胸主动脉瘤发病机制的影响
Int J Clin Exp Pathol. 2014 Oct 15;7(11):7643-52. eCollection 2014.
8
Previously differentiated medial vascular smooth muscle cells contribute to neointima formation following vascular injury.先前分化的血管内侧平滑肌细胞在血管损伤后有助于新生内膜的形成。
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LincRNA-p21 regulates neointima formation, vascular smooth muscle cell proliferation, apoptosis, and atherosclerosis by enhancing p53 activity.长链非编码 RNA-p21 通过增强 p53 活性来调节新生内膜形成、血管平滑肌细胞增殖、凋亡和动脉粥样硬化。
Circulation. 2014 Oct 21;130(17):1452-1465. doi: 10.1161/CIRCULATIONAHA.114.011675. Epub 2014 Aug 25.
10
Transdifferentiation of vascular smooth muscle cells to macrophage-like cells during atherogenesis.动脉粥样硬化形成过程中血管平滑肌细胞向巨噬细胞样细胞的转分化。
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颈动脉结扎后的炎症与血管平滑肌细胞去分化

Inflammation and vascular smooth muscle cell dedifferentiation following carotid artery ligation.

作者信息

Herring B Paul, Hoggatt April M, Griffith Sarah L, McClintick Jeanette N, Gallagher Patricia J

机构信息

Department of Cellular and Integrative Physiology, Indiana University School of Medicine, Indianapolis, Indiana; and

Department of Cellular and Integrative Physiology, Indiana University School of Medicine, Indianapolis, Indiana; and.

出版信息

Physiol Genomics. 2017 Mar 1;49(3):115-126. doi: 10.1152/physiolgenomics.00095.2016. Epub 2016 Dec 30.

DOI:10.1152/physiolgenomics.00095.2016
PMID:28039430
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5374455/
Abstract

Following vascular injury medial smooth muscle cells dedifferentiate and migrate through the internal elastic lamina where they form a neointima. The goal of the current study was to identify changes in gene expression that occur before the development of neointima and are associated with the early response to injury. Vascular injury was induced in C57BL/6 mice and in -creER(T2) mTmG reporter mice by complete ligation of the left carotid artery. Reporter mice were used to visualize cellular changes in the injured vessels. Total RNA was isolated from control carotid arteries or from carotid arteries 3 days following ligation of C57BL/6 mice and analyzed by Affymetrix microarray and quantitative RT-PCR. This analysis revealed decreased expression of mRNAs encoding smooth muscle-specific contractile proteins that was accompanied by a marked increase in a host of mRNAs encoding inflammatory cytokines following injury. There was also marked decrease in molecules associated with BMP, Wnt, and Hedgehog signaling and an increase in those associated with B cell, T cell, and macrophage signaling. Expression of a number of noncoding RNAs were also altered following injury with microRNAs 143/145 being dramatically downregulated and microRNAs 1949 and 142 upregulated. Several long noncoding RNAs showed altered expression that mirrored the expression of their nearest coding genes. These data demonstrate that following carotid artery ligation an inflammatory cascade is initiated that is associated with the downregulation of coding and noncoding RNAs that are normally required to maintain smooth muscle cells in a differentiated state.

摘要

血管损伤后,中膜平滑肌细胞去分化并穿过内弹力层迁移,在那里形成新内膜。本研究的目的是确定在新内膜形成之前发生的、与损伤早期反应相关的基因表达变化。通过完全结扎左颈动脉,在C57BL/6小鼠和 -creER(T2) mTmG报告基因小鼠中诱导血管损伤。使用报告基因小鼠来观察受损血管中的细胞变化。从对照颈动脉或C57BL/6小鼠结扎后3天的颈动脉中分离总RNA,并通过Affymetrix微阵列和定量RT-PCR进行分析。该分析显示,编码平滑肌特异性收缩蛋白的mRNA表达降低,同时损伤后大量编码炎性细胞因子的mRNA显著增加。与骨形态发生蛋白(BMP)、Wnt和Hedgehog信号相关的分子也显著减少,而与B细胞、T细胞和巨噬细胞信号相关的分子增加。损伤后一些非编码RNA的表达也发生了改变,其中微小RNA 143/145显著下调,微小RNA 1949和142上调。几种长链非编码RNA的表达改变反映了其最邻近编码基因的表达。这些数据表明,颈动脉结扎后引发了炎症级联反应,这与维持平滑肌细胞分化状态所需的编码和非编码RNA的下调有关。