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急性冠状动脉综合征患者淋巴细胞凋亡标志物Fas/FasL(CD95/CD95L)表达的分析

Analysis of apoptotic markers Fas/FasL (CD95/CD95L) expression on the lymphocytes in patients with acute coronary syndrome.

作者信息

Bossowska Anna, Bossowski Artur, Galar Bogdan

机构信息

Department of Cardiology, Internal Affair and Andministration Ministry Hospital, and Medical University, Białystok, Poland.

出版信息

Kardiol Pol. 2007 Aug;65(8):883-9; discussion 890-2.

Abstract

BACKGROUND

Acute coronary syndromes are caused by the rupture or erosion of an atherosclerotic plaque which by secreting a variety of proteases is capable of degrading pericellular matrix components induces death of endothelial cells. This mechanism plays the main role in apoptosis.

AIM

To estimate expression of apoptotic Fas/FasL (CD95/CD95L) on lymphocytes in the peripheral blood.

METHODS

We examined patients with acute myocardial infarction (n=18, mean age 62+/-8 years), in unstable angina pectoris (n=31, mean age 62+/-10 years) and in a control group (n=20, mean age 62+/-9 years) without coronary risk factors and inflammatory condition. All investigations of Fas/FasL were performed by flow cytometry. Inflammatory parameters and standard risk factors were investigated by standard methods (ELISA).

RESULTS

The analysis revealed a higher expression of Fas and FasL molecules on the lymphocytes from patients with acute myocardial infarction (p<0.001, p<0.002) and unstable angina (p<0.01, p<0.02) compared to the control group. Moreover we found a statistically significant positive correlation between the level of LDL cholesterol and hypertension and prevalence of CD95 (p<0.001, p<0.01) and CD95L (p<0.02, p<0.03) in patients with acute myocardial infarction.

CONCLUSIONS

A higher expression of apoptotic molecules (Fas and FasL) on lymphocytes occurs before the onset of acute ischaemia and contributes to the plaque rupture and acute coronary syndrome. Furthermore, antiapoptotic therapy leads to plaque stabilisation.

摘要

背景

急性冠状动脉综合征由动脉粥样硬化斑块破裂或糜烂引起,该斑块通过分泌多种蛋白酶能够降解细胞周围基质成分,从而诱导内皮细胞死亡。这种机制在细胞凋亡中起主要作用。

目的

评估外周血淋巴细胞上凋亡相关Fas/FasL(CD95/CD95L)的表达。

方法

我们检查了急性心肌梗死患者(n = 18,平均年龄62±8岁)、不稳定型心绞痛患者(n = 31,平均年龄62±10岁)以及无冠心病危险因素和炎症状态的对照组(n = 20,平均年龄62±9岁)。所有Fas/FasL检测均通过流式细胞术进行。炎症参数和标准危险因素通过标准方法(ELISA)进行检测。

结果

分析显示,与对照组相比,急性心肌梗死患者(p<0.001,p<0.002)和不稳定型心绞痛患者(p<0.01,p<0.02)淋巴细胞上Fas和FasL分子表达更高。此外,我们发现急性心肌梗死患者中,低密度脂蛋白胆固醇水平和高血压与CD95(p<0.001,p<0.01)及CD95L(p<0.02,p<0.03)的患病率之间存在统计学显著正相关。

结论

淋巴细胞上凋亡分子(Fas和FasL)的高表达在急性缺血发作前出现,并促成斑块破裂和急性冠状动脉综合征。此外,抗凋亡治疗可使斑块稳定。

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