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Microvesicles-mediated Cell Communnicationn in Pulmonary Arterial Hypertension

期刊

CURRENT MEDICINAL CHEMISTRY
卷 28, 期 23, 页码 4731-4741

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/0929867328666201124152406

关键词

Microvesicles; extracellular vesicles; cell communication; macrophage-derived microvesicles; inflammation; pulmonary arterial hypertension

资金

  1. National Natural Science Foundation of China [81973404, 81503058]
  2. Department of Education of Liaoning Province [JC2019034]
  3. Natural Science Founda-tion of Liaoning Province [2014021065]

向作者/读者索取更多资源

Microvesicles play an important role in the pathogenesis of pulmonary arterial hypertension by transferring inflammatory factors and may become a potential therapeutic target for the disease.
Background: Pulmonary arterial hypertension is one of the chronic diseases that affect human health. Microvesicles participate in the communication between cells by fusing with the recipient cells to transfer the bioactive molecules, such as lipids, proteins, RNA, etc., to the target cells. Microvesicles are involved in various biological processes and have the functions of regulating immunity, promoting angiogenesis, and so on. Microvesicles derived from various cells may become the diagnostic biomarkers or therapeutic targets for the diseases. Therefore, exploring the role of microvesicles-mediated cell communication has become a potential therapeutic target for pulmonary arterial hypertension. Objective: It is to clarify the classification, features, and mechanism of microvesicles in cell communication and to discuss the potentially important roles of microvesicles-mediated cell communication in pulmonary arterial hypertension. Results: Inflammation is an important pathogenesis of pulmonary arterial hypertension. Many studies have shown that microvesicles from different cells can participate in the pathological process of pulmonary arterial hypertension by transferring the inflammatory factors contained in them. Conclusion: Microvesicles-mediated cell communication may become the therapeutic target for pulmonary arterial hypertension.

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