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GDF15 在脓毒症中的临床价值及其潜在机制。

The Clinical Value of GDF15 and Its Prospective Mechanism in Sepsis.

机构信息

Department of Clinical Laboratory, Renmin Hospital of Wuhan University, Wuhan, China.

出版信息

Front Immunol. 2021 Sep 8;12:710977. doi: 10.3389/fimmu.2021.710977. eCollection 2021.

Abstract

Growth differentiation factor 15 (GDF15) is involved in the occurrence and development of many diseases, and there are few studies on its relationship with sepsis. This article aims to explore the clinical value of GDF15 in sepsis and to preliminarily explore its prospective regulatory effect on macrophage inflammation and its functions. We recruited 320 subjects (132 cases in sepsis group, 93 cases in nonsepsis group, and 95 cases in control group), then detected the serum GDF15 levels and laboratory indicators, and further investigated the correlation between GDF15 and laboratory indicators, and also analyzed the clinical value of GDF15 in sepsis diagnosis, severity assessment, and prognosis. , we used LPS to stimulate THP-1 and RAW264.7 cells to establish the inflammatory model, and detected the expression of GDF15 in the culture medium and cells under the inflammatory state. After that, we added GDF15 recombinant protein (rGDF15) pretreatment to explore its prospective regulatory effect on macrophage inflammation and its functions. The results showed that the serum GDF15 levels were significantly increased in the sepsis group, which was correlated with laboratory indexes of organ damage, coagulation indexes, inflammatory factors, and SOFA score. GDF15 also has a high AUC in the diagnosis of sepsis, which can be further improved by combining with other indicators. The dynamic monitoring of GDF15 levels can play an important role in the judgment and prognosis of sepsis. In the inflammatory state, the expression of intracellular and extracellular GDF15 increased. GDF15 can reduce the levels of cytokines, inhibit M1 polarization induced by LPS, and promote M2 polarization. Moreover, GDF15 also enhances the phagocytosis and bactericidal function of macrophages. Finally, we observed a decreased level of the phosphorylation of JAK1/STAT3 signaling pathway and the nuclear translocation of NF-κB p65 with the pretreatment of rGDF15. In summary, our study found that GDF15 has good clinical application value in sepsis and plays a protective role in the development of sepsis by regulating the functions of macrophages and inhibiting the activation of JAK1/STAT3 pathway and nuclear translocation of NF-κB p65.

摘要

生长分化因子 15(GDF15)参与多种疾病的发生和发展,关于其与脓毒症的关系研究较少。本研究旨在探讨 GDF15 在脓毒症中的临床价值,并初步探讨其对巨噬细胞炎症及其功能的潜在调控作用。我们招募了 320 名受试者(脓毒症组 132 例,非脓毒症组 93 例,对照组 95 例),检测血清 GDF15 水平和实验室指标,进一步分析 GDF15 与实验室指标的相关性,并分析 GDF15 在脓毒症诊断、严重程度评估和预后中的临床价值。我们使用 LPS 刺激 THP-1 和 RAW264.7 细胞建立炎症模型,检测炎症状态下培养基和细胞中 GDF15 的表达。然后,我们添加 GDF15 重组蛋白(rGDF15)预处理,探讨其对巨噬细胞炎症及其功能的潜在调控作用。结果表明,脓毒症组血清 GDF15 水平显著升高,与器官损伤、凝血指标、炎症因子和 SOFA 评分的实验室指标相关。GDF15 对脓毒症的诊断具有较高的 AUC,与其他指标联合应用可进一步提高。GDF15 水平的动态监测对脓毒症的判断和预后具有重要作用。在炎症状态下,细胞内和细胞外 GDF15 的表达增加。GDF15 可降低细胞因子水平,抑制 LPS 诱导的 M1 极化,并促进 M2 极化。此外,GDF15 还增强了巨噬细胞的吞噬和杀菌功能。最后,我们观察到 rGDF15 预处理后 JAK1/STAT3 信号通路磷酸化水平降低,NF-κB p65 核转位减少。综上所述,本研究发现 GDF15 在脓毒症中具有良好的临床应用价值,通过调节巨噬细胞功能,抑制 JAK1/STAT3 通路磷酸化和 NF-κB p65 核转位,在脓毒症的发生发展中发挥保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f761/8456026/b3a4f2470b7b/fimmu-12-710977-g001.jpg

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