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논문 기본 정보

자료유형
학술저널
저자정보
Yixi Chen (Hunan Environment-Biological Polytechnic College) Jianping Cao (Hunan Environment-Biological Polytechnic College) Qihui Zhao (Hunan Environment-Biological Polytechnic College) Haiyong Luo (Hunan Environment-Biological Polytechnic College) Yiguang Wang (Institute of Medicinal Biotechnology Chinese Academy of Medical Sciences) Wenjian Dai (Hunan Environment-Biological Polytechnic College)
저널정보
대한약리학회 The Korean Journal of Physiology & Pharmacology The Korean Journal of Physiology & Pharmacology 제22권 제2호
발행연도
2018.3
수록면
127 - 134 (8page)
DOI
https://doi.org/10.4196/kjpp.2018.22.2.127

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Myofibrillogenesis regulator-1 (MR-1) is a novel protein involved in cellular proliferation, migration, inflammatory reaction and signal transduction. However, little information is available on the relationship between MR-1 expression and the progression of atherosclerosis. Here we report atheroprotective effects of silencing MR-1 in a model of Ang II-accelerated atherosclerosis, characterized by suppression focal adhesion kinase (FAK) and nuclear factor kappaB (NF-κB) signaling pathway, and atherosclerotic lesion macrophage content. In this model, administration of the siRNA-MR-1 substantially attenuated Ang II-accelerated atherosclerosis with stabilization of atherosclerotic plaques and inhibited FAK, Akt, mammalian target of rapamycin (mTOR) and NF-kB activation, which was associated with suppression of inflammatory factor and atherogenic gene expression in the artery. In vitro studies demonstrated similar changes in Ang II-treated vascular smooth muscle cells (VSMCs) and macrophages: siRNA-MR-1 inhibited the expression levels of proinflammatory factor. These studies uncover crucial proinflammatory mechanisms of Ang II and highlight actions of silencing MR-1 to inhibit Ang II signaling, which is atheroprotective.

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