Roles of ROCK (Rho-associated protein kinase) and its Associated Pathways During Acute Vascular Thrombosis Events

論文翻譯標題: 急性血管栓塞中Rho激?蛋白和相關訊息傳遞路徑所扮演的角色
  • 王 裕文

學生論文: Master's Thesis

摘要

Acute myocardial infarction (AMI) is a leading cause of death of cardiovascular disease (CVD) in the world It can be triggered by thrombin which promotes thrombosis and causes coronary artery occlusion In early CVD monocyte and macrophage play major role in atherosclerosis and promote plaque formation partially via Rho kinase (ROCK) signal pathway However it remained unknown how ROCK signaling or its associated pathways play the role on monocytes and macrophages functions during the AMI development process Previous studies have shown that galectin-3 could promote inflammation cell migration and macrophage phagocytosis It is possible that galectin-3 may play as the mechanism between activation of macrophages or monocytes under thrombin stimulation thus facilitate ROCK activation Therefore our aim is to test the interaction between galectin-3 and Rho protein signal pathway in macrophages To investigate the ROCK activity ROCK expression and galectin-3 secretion in macrophages thrombin was used for the activation of THP-1 macrophage cell line After stimulation of thrombin in macrophages we studied the relationship between ROCK and galectin-3 secretion by western blots Then we tested the galectin-3 secretion among macrophage with ROCK inhibitor after thrombin stimulation Flow cytometry and migration assay were applied to detect the M1/M2 macrophage expression distribution and migration functional changes after thrombin treatment Finally to prove that ROCK is important in human acute thrombotic event we detected the phosphor-ezrin/radixin/moesin (pERM) which are the downstream molecules of ROCK and galectin-3 expression in macrophages isolated from AMI patient and also healthy donors We found that galectin-3 secretion was activated in macrophage after thrombin treatment peaking at 24 hours Interestingly Rho-associated pathway protein expressions increased after thrombin treatment earlier at 12 hours After Rho-kinase inhibitor treatment the expression of galectin-3 decreased in the activated macrophage Regarding functional assay more percentage of THP-1-derived macrophages were prone to become M1 type macrophage after thrombin treatment in flow cytometry and had greater migration ability after thrombin treatment Finally we proved that pERM and galectin-3 expression in AMI patient’s macrophages were higher than healthy donor’s macrophages In conclusion thrombin treatment can stimulate macrophage to M1 type and their migration ability thus promote Rho-kinase signal pathway expression and galectin-3 secretion
獎項日期2015 一月 21
原文English
監督員Ping-Yen Liu (Supervisor)

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