细胞外囊泡与心血管疾病相互关联:心脏病学的临床新视角

Swarup Sonar
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引用次数: 0

摘要

亲爱的编辑,细胞外囊泡(EVs)是从多个细胞中释放出来的细胞信号分子,可分为微囊泡、凋亡体和外泌体等多个亚群1 。目前,心血管疾病(CVD)已成为全球性的健康危机。3 全球与心血管疾病相关的最常见死亡原因是动脉粥样硬化的临床后果,如冠状动脉疾病和中风。冠状动脉疾病(CAD)是最常见的心脏并发症。导致冠状动脉疾病的一些因素包括内皮功能障碍、氧化应激和炎症途径的激活,以及动脉中胆固醇积累的增加。在 CAD 中,心肌细胞、干细胞、内皮细胞和血小板分泌的外泌体与 CAD 的发展有关。4 在 CAD 期间,外泌体 miRNA 的高表达具有临床意义(miRNA-1、miRNA-92、miRNA-30、miRNA-133、miRNA-208 和 miRNA-499 高表达)。在急性心肌梗死患者血浆中观察到外泌体衍生的 miRNA-133a、miRNA-208、miRNA-1 和 miRNA-499 高度富集。5 循环 miRNA 在心血管疾病中的血清学特征非常令人印象深刻。6 此外,还观察到 miRNA-221、miR-210、miRNA-126 和 miRNA-30 在中风事件中表达较低,而 miRNA-145 和 miRNA-21 在中风中表达较高。外泌体是一种很有前景的心血管疾病生物标志物来源。8 一些外泌体来源(干细胞衍生的外泌体或改良外泌体)也被用作心血管疾病的治疗手段。9, 10 外泌体研究面临的挑战包括外泌体异质性、大规模生产、分离等。单个外泌体分析11 解决了这一难题,为精准治疗学的发展提供了支持。未来,基于外泌体的治疗学应用将成为心血管疾病的有效解决方案:作者声明无利益冲突。
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Extracellular vesicles and cardiovascular disease interlink: A new clinical perspective in cardiology

Dear Editor,

Extracellular vesicles (EVs) are cell signalling molecules released from several cells. it is classified into several subpopulations such as microvesicles, apoptotic bodies, and exosomes.1 Current time exosomes reveal several disease complications effectively including cancer, immunological, neurological, and cardiology complications.2 Exosome carries dynamic molecular cargo such as DNA, RNAs, proteins, lipids, etc.1 This molecule indicates cellular status (health or cell undergoing any clinical complication). Cardiovascular disease (CVD) become a global bordering health crisis current time.3 The most common cause of CVD-related mortality globally is caused by the clinical consequences of atherosclerosis, such as coronary artery disease and stroke. Coronary artery disease (CAD) is the most common heart complication. Some factors develop it such as activation of endothelial dysfunction, oxidative stress, and inflammatory pathways, as well as enhanced cholesterol accumulation in the arteries. In CAD, cardiomyocytes, stem cells, endothelial cells, and platelets secreted exosomes related to the development of CAD.4 During CAD, higher expression of exosomes miRNA has clinical significance (miRNA-1, miRNA-92, miRNA-30, miRNA-133, miRNA-208, and miRNA-499 highly expressed). Exosome-derived miRNA-133a, miRNA-208, miRNA-1, and miRNA-499 high enrichment was observed in acute myocardial infarction patients plasma.5 Theranostic signature of circulation miRNAs in CVD is very impressive.6 Additionally, it was observed that miRNA-221, miR-210, miRNA-126 and miRNA-30 have lower expression in stroke incidents, other hand miRNA-145 and miRNA-21 were highly expressed in stroke.7 The exosome is a promising biomarker source of CVD.8 Several EV sources (stem cell-derived EVs or modified EVs) are also used in CVD as a therapeutic.9, 10 Exosome research-based challenges such as exosome heterogeneity, large-scale production, isolation, etc. Single exosome profiling11 solved this complication and supported the precision theranostics development. In the future, exosome-based theranostics applications become an effective solution for CVD.

Swarup Sonar: Manuscript writing; editing and reviewing.

The author declares no conflict of interest.

Not applicable.

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