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肥胖个体中内皮损伤的转化证据:炎症和促血栓形成反应。

Translational evidence of endothelial damage in obese individuals: inflammatory and prothrombotic responses.

机构信息

Endocrinology and Nutrition Department, Diabetes and Obesity Laboratory, Hospital Clinic/IDIBAPS, University of Barcelona, Barcelona, Spain.

出版信息

J Thromb Haemost. 2011 Jun;9(6):1236-45. doi: 10.1111/j.1538-7836.2011.04285.x.

Abstract

BACKGROUND

Obesity is associated with an increased atherothrombotic morbidity/mortality risk. However, there is no direct evidence of subclinical activation of the endothelium in obese subjects without other major cardiometabolic risk factors.

OBJECTIVES

We applied a translational approach to investigate endothelial activation occurring in response to the components secreted by visceral and subcutaneous adipose tissue and their corresponding cell fractions obtained from obese subjects without other major cardiometabolic risk factors, as compared with non-obese controls.

METHODS

Fat pads and cell fractions were incubated with serum-free medium to obtain their secretomes, which were analyzed by protein arrays. Endothelial cells (ECs) were exposed to the different secretomes to evaluate changes in gene expression, composition and reactivity of the extracellular matrix (ECM), and cell growth and viability.

RESULTS

ECs incubated in the presence of obese secretomes displayed increased proliferation, altered cell morphology, augmented expression of VCAM-1, ICAM-1, and von Willebrand factor, and higher ECM reactivity towards circulating platelets. The visceral secretomes, especially the stromal one, induced the strongest expression of these markers, together with a more reactive ECM. These changes occurred through nuclear factor-κB (NF-κB) activation.

CONCLUSION

This is the first translational study demonstrating that the cytokines secreted by the adipose tissue from obese individuals without other major cardiometabolic complications have a hazardous effect on the endothelium, through activation of the NF-κB pathway.

摘要

背景

肥胖与动脉粥样硬化血栓形成的发病率和死亡率增加有关。然而,在没有其他主要心血管代谢危险因素的肥胖患者中,并没有直接的证据表明内皮细胞存在亚临床激活。

目的

我们采用转化方法研究了来自没有其他主要心血管代谢危险因素的肥胖患者的内脏和皮下脂肪组织及其相应细胞成分分泌的成分引起的内皮细胞激活,并与非肥胖对照组进行了比较。

方法

用无血清培养基孵育脂肪垫和细胞成分以获得其分泌组,并用蛋白质芯片进行分析。将内皮细胞(ECs)暴露于不同的分泌组中,以评估基因表达、细胞外基质(ECM)的组成和反应性以及细胞生长和活力的变化。

结果

在肥胖分泌组存在的情况下孵育的 ECs 显示出增殖增加、细胞形态改变、VCAM-1、ICAM-1 和 von Willebrand 因子的表达增加,以及对循环血小板的 ECM 反应性增加。内脏分泌组,特别是基质分泌组,诱导这些标志物的最强表达,同时 ECM 反应性更高。这些变化是通过核因子-κB(NF-κB)激活发生的。

结论

这是第一项转化研究,证明了来自没有其他主要心血管代谢并发症的肥胖个体的脂肪组织分泌的细胞因子通过 NF-κB 途径对内皮细胞具有危害性影响。

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