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C1q/TNF 相关蛋白-15 和脂联素对冠心病患者原代巨噬细胞白细胞介素 6 和肿瘤坏死因子-α的影响。

The impacts of C1q/TNF-related protein-15 and adiponectin on Interleukin-6 and tumor necrosis factor-α in primary macrophages of patients with coronary artery diseases.

机构信息

Clinical Biochemistry Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran.

Sleep Disorders Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran.

出版信息

Cytokine. 2021 Jun;142:155470. doi: 10.1016/j.cyto.2021.155470. Epub 2021 Mar 3.

Abstract

UNLABELLED

Atherosclerosis is a progressive inflammatory disease characterized by the accumulation of lipids in the arterial wall. Inflammation plays a key role in the pathogenesis of atherosclerosis and some previous studies have shown the role of adipokines during the inflammatory process of atherosclerosis. Therefore, the present study aimed to evaluate the impacts of adiponectin and CTRP15 on inflammatory cytokines secretions from THP1 and primary macrophages.

METHODS

THP1 monocytes were differentiated to macrophages and primary monocytes were then isolated from patients with coronary artery disease and controls who were differentiated to macrophages. Macrophages were treated with LPS, LPS+adiponectin, and LPS+CTRP15.

RESULTS

Adiponectin and CTRP15 have reduced IL-6 and TNF-α secretions from LPS-induced THP1 macrophages, and the CTRP15 indicated a more potent anti-inflammatory property compared to adiponectin. In addition, adiponectin reduced cytokines' expressions and secretions in primary macrophages of both patient and control groups. However, CTRP15 has only reduced cytokines' expressions and secretions in controls and it was not able to ameliorate inflammation in macrophages of CAD patients.

CONCLUSION

The results of the present study indicate anti-inflammatory impact of adiponectin and CTRP15, while this property was stronger for CTRP15. In addition, it seems likely that anti-inflammatory CTRP15's impact on macrophages in the CAD patients was weaker than macrophages from the controls.

摘要

未加标签

动脉粥样硬化是一种渐进性炎症性疾病,其特征是脂质在动脉壁中的积累。炎症在动脉粥样硬化的发病机制中起着关键作用,一些先前的研究表明了脂肪因子在动脉粥样硬化炎症过程中的作用。因此,本研究旨在评估脂联素和 CTRP15 对 THP1 和原代巨噬细胞中炎症细胞因子分泌的影响。

方法

将 THP1 单核细胞分化为巨噬细胞,然后从冠心病患者和对照组中分离原代单核细胞分化为巨噬细胞。用 LPS、LPS+脂联素和 LPS+CTRP15 处理巨噬细胞。

结果

脂联素和 CTRP15 可减少 LPS 诱导的 THP1 巨噬细胞中 IL-6 和 TNF-α 的分泌,并且 CTRP15 比脂联素具有更强的抗炎作用。此外,脂联素可降低两组患者和对照组原代巨噬细胞中细胞因子的表达和分泌。然而,CTRP15 仅降低了对照组细胞因子的表达和分泌,并且不能改善 CAD 患者巨噬细胞中的炎症。

结论

本研究结果表明脂联素和 CTRP15 具有抗炎作用,而 CTRP15 的作用更强。此外,抗炎性 CTRP15 对 CAD 患者巨噬细胞的影响似乎弱于对照组的巨噬细胞。

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