急性肺栓塞患者外周血循环ACE2和Mas表达及其对内皮损伤的影响
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国家自然科学基金项目(82274131)


Expression of ACE2 and Mas in peripheral blood circulation and their effects on endothelial injury in patients with acute pulmonary embolism
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    摘要:

    目的 探究急性肺栓塞(APE)患者治疗前后外周血循环内皮细胞(CECs)凋亡数量及ACE2、Mas蛋白表达变化。方法 收集2023年1月—2023年10月本院急诊科接收的APE患者82例,根据疾病严重程度将其分为中高危组42例、低危组40例,另选取40例于本院体检的健康受试者为对照组。取APE患者入院时、出院时及健康受试者外周血。流式细胞术分析APE患者及健康受试者CECs数量、凋亡水平。Western blotting检测CECs内凋亡蛋白Bax、Bcl2、caspase 3/9水平变化及蛋白ACE2、Mas表达变化。结果 入院时中高危组、低危组患者入院时外周血CECs数量及凋亡率均显著高于对照组,且中高危组CECs数量及凋亡率均显著高于低危组水平(P<0.05)。出院时中高危组及低危组患者CECs数量及凋亡率均显著低于入院时水平(P<0.05)。入院时中高危组、低危组患者CECs中Bax/Bcl2蛋白比值、切割caspase 3/9蛋白水平显著高于对照组,且中高危组这些指标水平显著高于低危组,同时出院时中高危组、低危组患者CECs上述指标水平显著低于入院时水平(P<0.05)。进一步发现入院时中高危组、低危组CECs中ACE2、Mas水平显著低于对照组,且中高危组上述指标水平显著低于低危组(P<0.05)。结论 APE患者外周血CECs数量及凋亡率显著增加,治疗后CECs数量及凋亡率减少,提示CECs可能与APE发病及预后相关,同时ACE2-Mas轴可能参与调控CECs凋亡

    Abstract:

    Objective To investigate the apoptosis of peripheral blood circulating endothelial cells (CECs) and the expression of ACE2 and Mas protein in patients with acute pulmonary embolism (APE) before and after treatment. Methods A total of 82 patients with APE received by the emergency department of our hospital were collected and divided into medium-high risk group (n=42) and low risk group (n=40) according to the severity of the disease. Forty healthy subjects who underwent physical examination in our hospital were selected as the control group. Peripheral blood of APE patients at admission, discharge and healthy subjects was taken. Flow cytometry was used to analyze the number of CECs, and their apoptosis level and surface angiotensin converting enzyme 2 (ACE2) expression in peripheral blood of APE patients and healthy subjects. Western blotting was used to detect the levels of apoptotic proteins Bax, Bcl2, caspase 3/9 and the expression of proteins ACE2 and Mas in CECs. Results The number and apoptosis rate of CECs in peripheral blood of patients in the high-risk group and the low-risk group at admission were significantly higher than those in the control group, and the number and apoptosis rate of CECs in the high-risk group were significantly higher than those in the low-risk group (P<0.05). The number and apoptosis rate of CECs in the high-risk group and the low-risk group at discharge were significantly lower than those at admission (P<0.05). The levels of Bcl2 protein, Bcl2/Bax protein ratio and cleaved caspase 3/9 protein in CECs of patients in the middle-high-risk group and low-risk group at admission were significantly higher than those in the control group, and the levels of these indexes in the middle-high-risk group were significantly higher than those in the low-risk group. At the same time, the levels of the above indexes in CECs of patients in the middle-high-risk group and low-risk group at discharge were significantly lower than those at admission (P<0.05). It was further found that the levels of ACE2 and Mas in CECs of the middle-high risk group and the low-risk group were significantly lower than those of the control group at admission, and the levels of the above indexes in the middle-high risk group were significantly lower than those in the low-risk group (P<0.05). Conclusion The number and apoptosis rate of CECs in peripheral blood of patients with APE increased significantly, and the number and apoptosis rate of CECs decreased after treatment, suggesting that CECs may be related to the pathogenesis and prognosis of APE, and the ACE2-Mas axis may be involved in the regulation of CECs apoptosis

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  • 在线发布日期: 2025-01-17
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