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体内动脉粥样硬化研究方法的研究综述。

Survey of Approaches for Investigation of Atherosclerosis In Vivo.

机构信息

Cardiff School of Biosciences, Cardiff University, Cardiff, UK.

出版信息

Methods Mol Biol. 2022;2419:57-72. doi: 10.1007/978-1-0716-1924-7_4.

DOI:10.1007/978-1-0716-1924-7_4
PMID:35237958
Abstract

Although in vitro model systems are useful for investigation of atherosclerosis-associated processes, they represent simplification of complex events that occur in vivo, which involve interactions between many different cell types together with their environment. The use of animal model systems is important for more in-depth insights of the molecular mechanisms underlying atherosclerosis and for identifying potential targets for agents that can prevent plaque formation and even reverse existing disease. This chapter will provide a survey of such animal models and associated techniques that are routinely used for research of atherosclerosis in vivo.

摘要

虽然体外模型系统对于研究动脉粥样硬化相关过程非常有用,但它们代表了体内复杂事件的简化,这些事件涉及许多不同细胞类型及其环境之间的相互作用。动物模型系统的使用对于深入了解动脉粥样硬化的分子机制以及鉴定能够预防斑块形成甚至逆转现有疾病的潜在药物靶点非常重要。本章将介绍常用于体内动脉粥样硬化研究的此类动物模型和相关技术。

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Radiation Impacts Early Atherosclerosis by Suppressing Intimal LDL Accumulation.辐射通过抑制内膜 LDL 蓄积来影响早期动脉粥样硬化。
Circ Res. 2021 Feb 19;128(4):530-543. doi: 10.1161/CIRCRESAHA.119.316539. Epub 2021 Jan 5.
2
Harnessing Single-Cell RNA Sequencing to Better Understand How Diseased Cells Behave the Way They Do in Cardiovascular Disease.利用单细胞 RNA 测序更好地了解心血管疾病中病变细胞的行为方式。
Arterioscler Thromb Vasc Biol. 2021 Feb;41(2):585-600. doi: 10.1161/ATVBAHA.120.314776. Epub 2020 Dec 17.
3
Heterogeneity of T Cells in Atherosclerosis Defined by Single-Cell RNA-Sequencing and Cytometry by Time of Flight.
单细胞 RNA 测序和飞行时间流式细胞术定义的动脉粥样硬化中的 T 细胞异质性。
Arterioscler Thromb Vasc Biol. 2021 Feb;41(2):549-563. doi: 10.1161/ATVBAHA.120.312137. Epub 2020 Dec 3.
4
Microanatomy of the Human Atherosclerotic Plaque by Single-Cell Transcriptomics.单细胞转录组学解析人动脉粥样硬化斑块的微观解剖结构。
Circ Res. 2020 Nov 6;127(11):1437-1455. doi: 10.1161/CIRCRESAHA.120.316770. Epub 2020 Sep 28.
5
Myeloid deletion and therapeutic activation of AMPK do not alter atherosclerosis in male or female mice.髓系细胞缺失和 AMPK 的治疗性激活均不改变雌雄小鼠的动脉粥样硬化。
J Lipid Res. 2020 Dec;61(12):1697-1706. doi: 10.1194/jlr.RA120001040. Epub 2020 Sep 25.
6
TL1A inhibits atherosclerosis in apoE-deficient mice by regulating the phenotype of vascular smooth muscle cells.TL1A 通过调节血管平滑肌细胞的表型抑制载脂蛋白 E 缺陷小鼠的动脉粥样硬化。
J Biol Chem. 2020 Nov 27;295(48):16314-16327. doi: 10.1074/jbc.RA120.015486. Epub 2020 Sep 22.
7
Single Cell RNA-Sequencing for the Study of Atherosclerosis.用于动脉粥样硬化研究的单细胞RNA测序
J Lipid Atheroscler. 2019 Sep;8(2):152-161. doi: 10.12997/jla.2019.8.2.152. Epub 2019 Jul 30.
8
Small rodent models of atherosclerosis.动脉粥样硬化的小型啮齿动物模型。
Biomed Pharmacother. 2020 Sep;129:110426. doi: 10.1016/j.biopha.2020.110426. Epub 2020 Jun 20.
9
Single Cell RNA Sequencing in Atherosclerosis Research.单细胞 RNA 测序在动脉粥样硬化研究中的应用。
Circ Res. 2020 Apr 24;126(9):1112-1126. doi: 10.1161/CIRCRESAHA.119.315940. Epub 2020 Apr 23.
10
A perspective on targeting inflammation and cytokine actions in atherosclerosis.靶向动脉粥样硬化中的炎症和细胞因子作用的观点。
Future Med Chem. 2020 Apr;12(7):613-626. doi: 10.4155/fmc-2019-0301. Epub 2020 Mar 16.